WO2009050507A1 - Marqueurs pour le cancer colorectal - Google Patents

Marqueurs pour le cancer colorectal Download PDF

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WO2009050507A1
WO2009050507A1 PCT/GB2008/050938 GB2008050938W WO2009050507A1 WO 2009050507 A1 WO2009050507 A1 WO 2009050507A1 GB 2008050938 W GB2008050938 W GB 2008050938W WO 2009050507 A1 WO2009050507 A1 WO 2009050507A1
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base
human chromosome
increased risk
linkage therewith
disequilibrium linkage
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PCT/GB2008/050938
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English (en)
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Malcolm G. Dunlop
Harry Campbell
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The University Court Of The University Of Edinburgh
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    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6876—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
    • C12Q1/6883—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
    • C12Q1/6886—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material for cancer
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q2600/00—Oligonucleotides characterized by their use
    • C12Q2600/172—Haplotypes

Definitions

  • This invention relates to prediction of the susceptibility of an individual to colorectal cancer.
  • Basis for the prediction lies in relating an individual's genetic makeup, as through molecular analysis, to the genetic makeup of a population of individuals.
  • Colorectal cancer is the third most common cancer and the third most common cause of death from cancer for both men and women. Colorectal cancer is responsible for more deaths that are not due primarily to tobacco use than any other type of cancer and inflicts a huge financial burden. Early detection of some human tumors such as uterine cervical cancer has dramatically reduced mortality from this condition (Herzog, 2003). Early detection of colorectal cancer can reasonably be expected to prevent death from this condition by identifying patients at risk for the disease, or those with the disease in an early stage and allow life saving intervention. A validated genetic test for colorectal cancer predisposition will have clinical utility, allowing prevention of cancer mortality through targeted screening programs.
  • Genotypic complexity is reduced through linkage disequilibrium that exists across long segments of the human genome with restriction in the diversity of haplotypes observed (Daly et al, 2001 ; Rioux et al, 2001; Liu et al, 2004). That is, single nucleotide polymorphisms found at specific locations within the human genome are inherited in conjunction with nucleotides that can be polymorphic that are physically located near by.
  • allelic association between pairs of markers typically extends over 10-5Ok, although there is tremendous variability in the magnitude of association observed at any given distance (Clark et al, 1998; Kikuchi et al., 2003; Dunning et al, 2000; Abecasis et al, 2001).
  • Genome-wide data (Gabriel et al. , 2002; Reich et al, 2001; Dawson et al, 2002) supports the generality of this description as well as its application across populations. This confirms that measurement of single nucleotide polymorphisms at sites in tight linkage disequilibrium with adjacent genomic regions can provide information about the presence of diversity not just at sites actually measured, but also about large areas of the adjacent genome.
  • STR short tandem repeats
  • VNTR variable number of tandem repeats
  • SSR short sequence repeats
  • micro satellites These repeats commonly are comprised of 1 to 5 base pairs. Polymorphism occurs due to variation in the number of repeated sequences found at a particular locus.
  • SNPs single nucleotide polymorphisms or SNPs. SNPs account for as much as 90% of human DNA polymorphism (Collins et al, 1998). SNPs are single base pair positions in genomic DNA at which different sequence alternatives (genotypes) exist in a population. By common definition, the least frequent allele occurs at least 1% of the time. These nucleotide substitutions may be a transition, which is the substitution of one purine by another purine or the substitution of one pyrimidine by another, or they may be transversions in which a purine is replaced by a pyrimidine or vice versa.
  • SNPs are observed in about 1 in 1000 base pairs (Wang el al, 1998; Taillon-Miller et al. , 1999).
  • the frequency of SNPs varies with the type and location of the change. Specifically, two-thirds of the substitutions involve the C o T (G « A) type, which may occur due to 5-methylcytosine deamination reactions that occur commonly. SNPs occur at a much higher frequency in non-coding regions than they do in coding regions.
  • This invention thus includes methods for identifying a subject at risk of colorectal cancer and/or determining risk of colorectal cancer in a subject, which comprise detecting the presence or absence of one or more polymorphic variations associated with colorectal cancer in a nucleic acid sample from the subject.
  • the present invention provides a method for detecting whether or not a subject has an altered risk of developing colorectal cancer, said method comprising the step of detecting the presence or absence of one or more polymorphic variations associated with colorectal cancer in a nucleic acid sample from a subject, wherein the polymorphic variations associated with colorectal cancer are in any one or more of the following nucleotide bases: a base located at position 113578406 on human chromosome 4; a base located at position 31114834 to position 31244811 on human chromosome 6; a base located at position 31114834 to position 31428789 on human chromosome 6; a base located at position 311 18992 to position 31220054 on human chromosome 6; a base located at position 31162490 to position 31461308 on human chromosome 6; a base located at position 31189184 to position 31454600 on human chromosome 6; a base located at position 31189184 to
  • the polymorphic variations may comprise mutations, for example point mutations, or the inversion, deletion and/or addition of one or more nucleotides.
  • the polymorphic variations associated with colorectal cancer are single nucleotide polymorphisms (SNPs).
  • this invention relates to identifying an individual who is at altered risk for developing colorectal cancer based on the presence of specific genotypes defined by 21 single nucleotide polymorphism (SNPs), observed alone or in combination.
  • SNPs single nucleotide polymorphism
  • the methods for identifying a subject at risk of colorectal cancer and/or determining the risk of colorectal cancer in a subject involves the detection of the presence or absence of one or more of the single nucleotide polymorphisms listed in Tables 1 to 21.
  • the method may not involve the SNPs presented in Tables 19 and 20 (i.e. those occurring at positions 44707461 and 44707927 of chromosome 18 or represented as SNPs rs 4939827 and rsl2953717).
  • the method may involve any variation occurring at any of the above noted positions and/or each of the SNPs presented in Tables I to 21.
  • one aspect of the present invention provides a method of determining or for diagnosing, a genetic predisposition to colorectal cancer in a subject, comprising providing or obtaining a sample containing at least one polynucleotide from the subject and analyzing the polynucleotide to detect the genetic polymorphism wherein the presence or absence of the polymorphism is associated with an altered susceptibility to developing colorectal cancer.
  • one or more of the 21 polymorphisms found distributed among 8 genes that we have identified may be used.
  • Another aspect of the present invention provides an isolated nucleic acid sequence comprising at least 16 contiguous nucleotides or their complements found in the genomic sequences of the 8 genes adjacent to and including the 21 polymorphic sites the inventors have identified to be associated with colorectal cancer.
  • Yet another aspect of the invention provides a method or medicament for treating colorectal cancer comprising providing or obtaining a sample of biological material containing at least one polynucleotide from the subject, analyzing the polynucleotides to detect the presence of at least one polymorphism associated with colorectal cancer and treating or administering the subject a medicament to counteract the effect of any such polymorphism detected.
  • the present invention may provide a method of recommending a treatment or medicament for colorectal cancer, said method comprising the steps of providing or obtaining a sample of biological material containing at least one polynucleotide from a subject, analyzing the polynucleotides to detect the presence of at least one polymorphism associated with colorectal cancer and recommending a therapy or medicament suitable for counteracting the effect of any such polymorphism detected.
  • Still another aspect of the invention provides a method or medicament for the prophylactic treatment of a subject identified with a genetic predisposition to colorectal cancer identified through the measurement of all or some of the 21 polymorphic SNP markers described in Tables 1 to 21.
  • prophylactic encompasses the act of administering a medicament or composition to prevent or protect against the onset of a particular disease or condition, hi this case, a method or medicament for use in prophylactically treating colorectal cancer may prevent or protect against the development of this disease in those subjects identified by any of the methods described herein, as being at risk of developing, or susceptible to, colorectal cancer.
  • Tables 1 to 21 report the result of a genotyping analysis of 4,669 samples by measuring 99,632 single nucleotide polymorphisms in peripheral blood DNA from 2,475 subjects (1,234 cases with colorectal cancer and 1,241 age matched individuals undiseased at the time of testing), and validating the identified CRC-associated alleles by using peripheral blood DNA from a second, different, group of 2,194 subjects (1,139 cases with colorectal cancer and 1 ,055 age matched individuals undiseased at the time of testing).
  • SEQ ID NOs: 1 to 260 are associated with an altered risk of developing colorectal cancer in subjects.
  • the present invention thus provides SNPs associated with colorectal cancer, nucleic acid molecules containing SNPs, methods and reagents for the detection of Che SNPs disclosed herein, uses of these SNPs for the development of detection reagents, and assays or kits that utilize such reagents.
  • the colorectal cancer-associated SNPs disclosed herein are useful for detecting, diagnosing, screening for, and evaluating predisposition to colorectal cancer and related pathologies in humans.
  • SNPs and their encoded products are useful targets for the development of therapeutic agents which, for example, may be used in the preparation or manufacture of medicaments for treating colorectal cancer and related disorders.
  • a large number of colorectal cancer-associated SNPs have been identified by genotyping DNA from 4,669 individuals, 2,373 of these individuals having been previously diagnosed with colorectal cancer and 2,296 being "control" or individuals thought to be free of colorectal cancer.
  • the present invention thus provides individual SNPs associated with colorectal cancer, genomic sequences (SEQ ID NOs:261 to 268) containing SNPs, transcript sequences and amino acid sequences.
  • the invention includes methods of detecting these polymorphisms in a test sample, methods of determining the risk of an individual of having or developing colorectal cancer, methods of screening for compounds useful for treating disorders associated with a variant gene/protein such as colorectal cancer, compounds identified by these screening methods, methods of using the disclosed SNPs to select, recommend or allocate a treatment strategy, methods of treating a disorder associated with a variant gene/protein (i.e., therapeutic methods), medicaments and methods of using the SNPs of the present invention for human identification.
  • this effect can be a "dominant” effect in which case such increased probability exists when the base is present in one or the other or both, alleles of the individual.
  • the effect can be said to be "recessive", in which case such increased probability exists only when the base is present in both alleles of the individual.
  • An "altered risk” means either an increased or a decreased risk.
  • a SNP is a particular type of polymorphic site, a polymorphic site being a region in a nucleic acid sequence at which two or more alternative nucleotides are observed in a significant number of individuals from a population.
  • a polymorphic site may be a nucleotide sequence of two or more nucleotides, an inserted nucleotide or nucleotide sequence, a deleted nucleotide or nucleotide sequence, or a microsatellite, for example.
  • a polymorphic site that is two or more nucleotides in length may be 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15 or more, 20 or more, 30 or more, 50 or more, 75 or more, 100 or more, 500 or more, or about 1000 nucleotides in length, where all or some of the nucleotide sequences differ within the region.
  • Each of the specific polymorphic sites found in SEQ ID NOs:261 to 268 is a "single nucleotide polymorphism" or a "SNP.”
  • each nucleotide sequence is referred to as a "polymorphic valiant" or "nucleic acid variant.”
  • polymorphic valiant or "nucleic acid variant.”
  • polymorphic variants represented in a majority of samples from a population
  • prevalent allele the polymorphic variant represented in a majority of samples from a population
  • polymorphic variant that is less prevalently represented is sometimes referred to as an "uncommon allele.”
  • An individual who possesses two prevalent alleles or two uncommon alleles is “homozygous” with respect to the polymorphism, and an individual who possesses one prevalent allele and one uncommon allele is "heterozygous” with respect to the polymorphism.
  • Individuals who are homozygous with respect to one allele are sometimes predisposed to a different phenotype as compared to individuals who are heterozygous or homozygous with respect to another allele.
  • a genotype or polymorphic variant may also be expressed in terms of a "haplotype,” which refers to the identity of two or more polymorphic variants occurring within genomic DNA on the same strand of DNA.
  • haplotype refers to the identity of two or more polymorphic variants occurring within genomic DNA on the same strand of DNA.
  • two SNPs may exist within a gene where each SNP position may include a cytosine variation or an adenine variation.
  • Certain individuals in a population may carry an allele (heterozygous) or two alleles (homozygous) having the gene with a cytosine at each SNP position.
  • the two cytosines corresponding to each SNP in the gene travel together on one or both alleles in these individuals, the individuals can be characterized as having a cytosine/cytosine haplotype with respect to the two SNPs in the gene.
  • a "phenotype” is a trait which can be compared between individuals, such as presence or absence of a condition, for example, occurrence of colorectal cancer.
  • Polymorphic variants are often reported without any determination of whether the variant is represented in a significant fraction of a population. Some reported variants are sequencing errors and/or not biologically relevant. Thus, it is often not known whether a reported polymorphic variant is statistically significant or biologically relevant until the presence of the variant is detected in a population of individuals and the frequency of the variant is determined.
  • a polymorphic variant may be detected on either or both strands of a double-stranded nucleic acid.
  • a polymorphic variant may be located within an intron or exon of a gene or within a portion of a regulatory region such as a promoter, a 5 1 untranslated region (UTR), a 3' UTR, and in DNA (e.g., genomic DNA (gDNA) and complementary DNA (cDNA)), RNA (e.g., mRNA, tRNA, and rRNA), or a polypeptide.
  • Polymorphic variations may or may not result in detectable differences in gene expression, polypeptide structure, or polypeptide function.
  • polymorphic variants can travel together. Such variants are said to be in "linkage disequilibrium" so that heritable elements e.g., alleles that have a tendency to be inherited together instead of being inherited independently by random assortment are in linkage disequilibrium. Alleles are randomly assorted or inherited independently of each other if the frequency of the two alleles together is the product of the frequencies of the two alleles individually. For example, if two alleles at different polymorphic sites are present in 50% of the chromosomes in a population, then they would be said to assort randomly if the two alleles are present together on 25% of the chromosomes in the population. A higher percentage would mean that the two alleles are linked.
  • a first polymorphic site Pl having two alleles, e.g. A and C--each appearing in 50% of the individuals in a given population is said to be in linkage disequilibrium with a second polymorphic site P2 having two alleles e.g. G and T-- each appearing in 50% of the individuals in a given population, if particular combinations of alleles are observed in individuals at a frequency greater than 25% (if the polymorphic sites are not linked, then one would expect a 50% chance of an individual having A at Pl and a 50% chance of having G at P2 thus leading to a 25% chance of having the combination of A at Pl and G at P2 together).
  • Heritable elements that are in linkage disequilibrium are said to be "linked” or "genetically linked" to each other.
  • each SNP in the genomic sequences identified as SEQ ID NOs: 261 to 268 is associated with the occurrence of colorectal cancer.
  • methods for identifying a risk of colorectal cancer in a subject which includes detecting the presence or absence of one or more of the SNPs described herein in a human nucleic acid sample.
  • Three different analyses were performed for each marker: (a) a test of trend across the 3 genotypes (Sasieni et al.
  • A A (adenine)
  • C cytosine
  • G G (guanine)
  • 4 T (thymidine).
  • B indicates the polymorphic allele.
  • AA, AB, BB are the counts of the number of individuals with the given genotype, by cases/controls. For dominant models, an odds ratio measuring the increase in risk associated with one or two copies of allele B is calculated. For recessive models, an odds ratio associated with exactly two copies of allele B is calculated. For the trend models, the Mantel- Haenszel odds ratio showing the increase in risk with each additional copy of allele B is calculated.
  • each polymorphic variation in the genomic sequences identified as SEQ ID NOs:261 to 268 is associated with the occurrence of colorectal cancer.
  • methods for identifying a risk of colorectal cancer in a subject which comprises detecting the presence or absence of one or more of the polymorphic variations described herein in a human nucleic acid sample.
  • the polymorphic variation, SNP are detailed in the tables.
  • Methods for determining whether a subject is susceptible to, i.e., at risk of colorectal cancer are provided herein. These methods include detecting the presence or absence of one or more polymorphic variations, i.e., SNPs 5 associated with colorectal cancer in a sample from a subject.
  • SNPs can be associated with a disease state in humans or in animals.
  • the association can be direct, as in conditions where the substitution of a base results in alteration of the protein coding sequence of a gene which contributes directly to the pathophysiology of the condition. Common examples of this include diseases such as sickle cell anemia and cystic fibrosis.
  • the association can be indirect when the SNP plays no role in the disease, but is located close to the defective gene such that there is a strong association between the presence of the SNP and the disease state. Because of the high frequency of SNPs within the genome, there is a greater probability that a SNP will be linked to a genetic locus of interest than other types of genetic markers.
  • Disease-associated SNPs can occur in coding and non-coding regions of the genome. When located in the coding region altered function of the ensuing protein sequence may occur. If it occurs in the regulatory region of a gene it may affect expression of the protein. If the protein is involved in protecting the body against pathological conditions this can result in disease susceptibility.
  • Nucleic acids for diagnosis may be obtained from a patient's cells, such as from blood, urine, saliva, tissue biopsy and autopsy material.
  • the genomic DNA may be used directly for detection or may be amplified enzymatically by using PCR prior to analysis (Saiki et al. , 1986).
  • RNA or cDNA may also be used in the same ways.
  • PCR primers complementary to the nucleic acid of one or more SNPs of the present invention can be used to identify and analyze the presence or absence of the SNP. For example, deletions and insertions can be detected by a change in size of the amplified product in comparison to the normal genotype.
  • Point mutations can be identified by hybridizing amplified DNA to radiolabeled SNP RNA of the present invention or alternatively, radiolabeled SNP antisense DNA sequences of the present invention.
  • Sequence differences between a reference gene and genes having mutations also may be revealed by direct DNA sequencing.
  • cloned DNA segments may be employed as probes to detect specific DNA segments. The sensitivity of such methods can be greatly enhanced by appropriate use of PCR or another amplification method.
  • a sequencing primer is used with double-stranded PCR product or a single-stranded template molecule generated by a modified PCR. The sequence determination is performed by conventional procedures with radiolabeled nucleotide or by automatic sequencing procedures with fluorescent-tags.
  • DNA sequence differences may be achieved by detection of alteration in electrophoretic mobility of DNA fragments in gels, with or without denaturing agents. Small sequence deletions and insertions can be visualized by high resolution gel electrophoresis. DNA fragments of different sequences may be distinguished on denaturing formamide gradient gels in which the mobilities of different DNA fragments are retarded in the gel at different positions according to their specific melting or partial melting temperatures (Myers et al, 1985).
  • Sequence changes at specific locations also may be revealed by nuclease protection assays, such as RNase and Sl protection or the chemical cleavage method (Cotton et al., 1988).
  • the detection of a specific DNA sequence may be achieved by methods which include, but are not limited to, hybridization, RNase protection, chemical cleavage, direct DNA sequencing or the use of restriction enzymes, (e.g., restriction fragment length polymorphisms ("RFLP”) and Southern blotting of genomic DNA).
  • restriction enzymes e.g., restriction fragment length polymorphisms ("RFLP") and Southern blotting of genomic DNA.
  • mutations also can be detected by in situ analysis.
  • Genetic mutations can be identified by hybridizing a sample and control nucleic acids, e.g., DNA or RNA, to high density arrays containing hundreds or thousands of oligonucleotide probes (Cronin et al, 1996; Kozal et al, 1996). For example, genetic mutations can be identified in two-dimensional arrays containing light-generated DNA probes as described in Cronin et al., supra. Briefly, a first hybridization array of probes can be used to scan through long stretches of DNA in a sample and control to identify base changes between the sequences by making linear arrays of sequential overlapping probes. This step allows the identification of point mutations.
  • This step is followed by a second hybridization array that allows the characterization of specific mutations by using smaller, specialized probe arrays complementary to all variants or mutations detected.
  • Each mutation array is composed of parallel probe sets, one complementary to the wild-type gene and the other complementary to the mutant gene.
  • Specific mutations can also be determined through direct sequencing of one or both strands of DNA using dideoxy nucleotide chain termination chemistry, electrophoresis through a semi- solid matrix and fluorescent or radioactive chain length detection techniques. Further mutation detection techniques may involve differential susceptibility of the polymorphic double strand to restriction endonuclease digestion, or altered electrophoretic gel mobility of single or double stranded gene fragments containing one polymorphic form.
  • Other techniques to detect specific DNA polymorphisms or mutation may involve evaluation of the structural characteristics at the site of polymorphism using nuclear magnetic resonance or x-ray diffraction techniques.
  • the invention includes a method for identifying a subject at risk of colorectal cancer, which includes detecting in a nucleic acid sample from or provided by the subject the presence or absence of a SNP associated with colorectal cancer at a polymorphic site in a nucleotide sequence identified as SEQ ID NOs: 1 to 268 .
  • Results from prognostic tests may be combined with other test results to diagnose colorectal cancer.
  • prognostic results may be gathered, a patient sample may be ordered based on a determined predisposition to colorectal cancer, the patient sample analyzed, and the results of the analysis may be utilized to diagnose colorectal cancer.
  • colorectal cancer diagnostic methods can be developed from studies used to generate prognostic/diagnostic methods in which populations are stratified into subpopulations having different progressions of colorectal cancer.
  • prognostic results may be gathered; a patient's risk factors for developing colorectal cancer analyzed (e.g., age, family history); and a patient sample may be ordered based on a determined predisposition to colorectal cancer.
  • the results from predisposition analyses may be combined with other test results indicative of colorectal cancer, which were previously, concurrently, or subsequently gathered with respect to the predisposition testing.
  • the combination of the prognostic test results with other test results can be probative of colorectal cancer, and the combination can be utilized as a colorectal cancer diagnostic.
  • Risk of colorectal cancer sometimes is expressed as a probability, such as an odds ratio, percentage, or risk factor.
  • the risk is based upon the presence or absence of one or more of the SNP variants described herein, and also may be based in part upon phenotypic traits of the individual being tested. Methods for calculating risk based upon patient data are well known (Agresti, 2001). Allelotyping and genotyping analyses may be carried out in populations other than those exemplified herein to enhance the predictive power of the prognostic method. These further analyses are executed in view of the exemplified procedures described herein, and may be based upon the same polymorphic variations or additional polymorphic variations. Risk determinations for colorectal cancer are useful in a variety of applications.
  • colorectal cancer risk determinations are used by clinicians to direct appropriate detection, preventative and treatment procedures to subjects who most require these. In another embodiment, colorectal cancer risk determinations are used by health insurers for preparing actuarial tables and for calculating insurance premiums.
  • the nucleic acid sample typically is isolated from a biological sample provided by or obtained from a subject.
  • nucleic acid can be isolated from blood, saliva, sputum, urine, cell scrapings, and biopsy tissue.
  • the nucleic acid sample can be isolated from a biological sample using standard techniques.
  • the nucleic acid sample may be isolated from the subject and then directly utilized in a method for determining the presence of a polymorphic variant, or alternatively, the sample may be isolated and then stored (e.g., frozen) for a period of time before being subjected to analysis.
  • the presence or absence of a polymorphic variant is determined using one or both chromosomal complements represented in the nucleic acid sample. Determining the presence or absence of a polymorphic variant in both chromosomal complements represented in a nucleic acid sample is useful for determining the zygosity of an individual for the polymorphic variant (i.e., whether the individual is homozygous or heterozygous for the polymorphic variant). Any oligonucleotide-based diagnostic may be utilized to determine whether a sample includes the presence or absence of a polymorphic variant in a sample. For example, primer extension methods, ligase sequence determination methods (e.g., U.S. Pat. Nos.
  • mismatch sequence determination methods e.g., U.S. Pat. Nos. 5,851,770; 5,958,692; 6,110,684; and 6,183,958
  • microarray sequence determination methods restriction fragment length polymorphism (RFLP), single strand conformation polymorphism detection (SSCP) (e.g., U.S. Pat. Nos. 5,891,625 and 6,013,499)
  • PCR-based assays e.g., TAQMANTM PCR System (Applied Biosystems)
  • nucleotide sequencing methods may be used.
  • Oligonucleotide extension methods typically involve providing a pair of oligonucleotide primers in a polymerase chain reaction (PCR) or in other nucleic acid amplification methods for the purpose of amplifying a region from the nucleic acid sample that comprises the polymorphic variation.
  • PCR polymerase chain reaction
  • One oligonucleotide primer is complementary to a region 3' of the polymorphism and the other is complementary to a region 5' of the polymorphism.
  • a PCR primer pair may be used in methods disclosed in U.S. Pat. Nos. 4,683,195; 4,683,202, 4,965,188; 5,656,493; 5,998,143; 6,140,054; WO 01/27327; and WO 01/27329 for example.
  • PCR primer pairs may also be used in any commercially available machines that perform PCR, such as any of the GENEAMPTM, systems available from Applied Biosystems. Also, those of ordinary skill in the art will be able to design oligonucleotide primers based upon the nucleotide sequences set forth in SEQ ID NOs: 1 to 268.
  • an extension oligonucleotide that hybridizes to the amplified fragment adjacent to the polymorphic variation.
  • An adjacent fragment refers to the 3' end of the extension oligonucleotide being often 1 nucleotide from the 5 r end of the polymorphic site, and sometimes 2, 3, 4, 5, 6, 7, 8, 9, or 10 nucleotides from the 5' end of the polymorphic site, in the nucleic acid when the extension oligonucleotide is hybridized to the nucleic acid.
  • the extension oligonucleotide then is extended by one or more nucleotides, and the number and/or type of nucleotides that are added to the extension oligonucleotide determine whether the polymorphic variant is present.
  • Oligonucleotide extension methods are disclosed, for example, in U.S. Pat. Nos. 4,656,127; 4,851,331; 5,679,524; 5,834,189; 5,876,934; 5,908,755; 5,912,118; 5,976,802; 5,981,186; 6,004,744; 6,013,431 ; 6,017,702; 6,046,005; 6,087,095; 6,210,891; and WO 01/20039. Oligonucleotide extension methods using mass spectrometry are described, for example, in U.S. Pat. Nos.
  • Multiple extension oligonucleotides may be utilized in one reaction, which is referred to as multiplexing.
  • a microarray can be utilized for determining whether a SNP is present or absent in a nucleic acid sample.
  • a microarray may include any oligonucleotides described herein, and methods for making and using oligonucleotide microarrays suitable for diagnostic use are disclosed in U.S. Pat. Nos.
  • the microarray typically comprises a solid support and the oligonucleotides may be linked to this solid support by covalent bonds or by non-covalent interactions.
  • the oligonucleotides may also be linked to the solid support directly or by a spacer molecule.
  • a microarray may comprise one or more oligonucleotides complementary to a SNP set forth in the tables.
  • a kit also may be utilized for determining whether a polymorphic variant is present or absent in a nucleic acid sample.
  • a kit can include one or more pairs of oligonucleotide primers useful for amplifying a fragment of a nucleotide sequence of interest, where the fragment includes a polymorphic site.
  • the kit sometimes comprises a polymerizing agent, for example, a thermo-stable nucleic acid polymerase such as one disclosed in U.S. Pat. Nos. 4,889,818 or 6,077,664.
  • the kit often comprises an elongation oligonucleotide that hybridizes to the nucleotide sequence in a nucleic acid sample adjacent to the polymorphic site.
  • kit includes an elongation oligonucleotide
  • it can also include chain elongating nucleotides, such as dATP, dTTP, dGTP, dCTP, and dITP, including analogs of dATP, dTTP, dGTP, dCTP and dITP, provided that such analogs are substrates for a thermo-stable nucleic acid polymerase and can be incorporated into a nucleic acid chain elongated from the extension oligonucleotide.
  • chain elongating nucleotides would be one or more chain terminating nucleotides such as ddATP, ddTTP, ddGTP, ddCTP.
  • the kit can include one or more oligonucleotide primer pairs, a polymerizing agent, chain elongating nucleotides, at least one elongation oligonucleotide, and one or more chain terminating nucleotides.
  • Kits optionally include buffers, vials, rm ' crotiter plates, and instructions for use.
  • An individual identified as being susceptible to colorectal cancer may be heterozygous or homozygous with respect to the allele associated with an increased risk of colorectal cancer, as indicated in the tables.
  • a subject homozygous for an allele associated with an increased risk of colorectal cancer is at a comparatively high risk of colorectal cancer as far as that SNP is concerned whether or not the allelic effect has been determined to be dominant or recessive.
  • a subject who is heterozygous for an allele associated with an increased risk of colorectal cancer, in which the allelic effect is recessive would likely be at a comparatively reduced risk of colorectal cancer predicted by that SNP.
  • Individuals carrying mutations in one or more SNP of the present invention may be detected at the protein level by a variety of techniques.
  • Cells suitable for diagnosis may be obtained from a patient's blood, urine, saliva, tissue biopsy and autopsy material.
  • Oligonucleotides can be linked to a second moiety, which can be another nucleic acid molecule to provide, for example, a tail sequence (e.g., a polyadenosine tail), an adapter sequence (e.g., phage Ml 3 universal tail sequence), etc.
  • the moiety might be one that facilitates linkage to a solid support or a detectable label, e.g., a radioactive label, a fluorescent label, a chemilumine scent label, a paramagnetic label, etc.
  • Nucleic acid sequences shown in the tables can be used for diagnostic or detection purposes or for detection and control of polypeptide expression.
  • oligonucleotide sequences such as antisense RNA, small- interfering RNA (siRNA) and DNA molecules and ribozymes that function to inhibit translation of a polypeptide are part of this invention.
  • Nucleic acids of the instant invention may be useful in the manufacture of medicaments for the treatment of colorectal cancer and/or associated disorders.
  • Antisense RNA and DNA molecules, siRNA and ribozymes can be prepared by known methods. These include techniques for chemically synthesizing oligodeoxyribonucleotides such as solid phase phosphoramidite chemical synthesis. Alternatively, RNA molecules may be generated by in vitro and in vivo transcription of DNA sequences encoding the antisense RNA molecule. Such DNA sequences can be incorporated into vectors which incorporate suitable RNA polymerase promoters such as the T7 or SP6 polymerase promoters, or antisense cDNA constructs that synthesize antlsense RNA constitutively or inducibly, depending on the promoter used, can be introduced stably into cell lines.
  • suitable RNA polymerase promoters such as the T7 or SP6 polymerase promoters
  • antisense cDNA constructs that synthesize antlsense RNA constitutively or inducibly, depending on the promoter used, can be introduced stably into cell lines.
  • DNA encoding a polypeptide can also be used in the analysis or diagnosis of colorectal cancer, resulting from aberrant expression of a target gene.
  • the nucleic acid sequence can be used in hybridization assays of biopsies or autopsies to diagnose or detect abnormalities of expression or function (e.g., Southern or Northern blot analysis, in situ hybridization assays).
  • Expression of a polypeptide during embryonic development can also be determined using nucleic acid encoding the polypeptide, particularly production of a functionally impaired polypeptide that is the cause of colorectal cancer.
  • In situ hybridizations using a polypeptide as a probe can be employed to predict problems related to colorectal cancer.
  • Administration of human active polypeptide, recombinantly produced can be used to treat disease states related to functionally impaired polypeptide.
  • gene therapy approaches may be employed to remedy deficiencies of functional polypeptide or to replace or compete with a dysfunctional polypeptide.
  • nucleic acid vectors include a nucleotide sequence set forth in the tables.
  • a vector is a nucleic acid molecule capable of transporting another nucleic acid to which it has been linked and can include a plasmid, cosmid, or viral vector.
  • the vector can be capable of autonomous replication or it can integrate into a host DNA.
  • Viral vectors may include replication defective retroviruses, adenoviruses and adeno-associated viruses for example.
  • a vector can include a nucleotide sequence from the tables in a form suitable for expression of an encoded protein or nucleic acid in a host cell.
  • the recombinant expression vector generally includes one or more regulatory sequences operatively linked to the nucleic acid sequence to be expressed.
  • a regulatory sequence includes promoters, enhancers and other expression control elements (e.g., polyadenylation signals). Regulatory sequences include those that direct constitutive expression of a nucleotide sequence, as well as tissue-specific regulatory and/or inducible sequences.
  • the design of the expression vector can depend on such factors as the choice of the host cell to be transformed, the level of expression of polypeptide desired, etc. Expression vectors can be introduced into host cells to produce the desired polypeptides, including fusion polypeptides.
  • Recombinant expression vectors can be designed for expression of polypeptides in prokaryotic or eukaryotic cells.
  • the polypeptides can be expressed in E. coli, insect cells (e.g., using baculovirus expression vectors), yeast cells, or mammalian cells. Suitable host cells are discussed further by Goeddel (Goeddel, 1990).
  • a recombinant expression vector can also be transcribed and translated in vitro, for example using T7 promoter regulatory sequences and T7 polymerase.
  • Fusion vectors add a number of amino acids to a polypeptide.
  • Such fusion vectors typically serve to increase expression of recombinant polypeptide, to increase the solubility of the recombinant polypeptide and/or to aid in the purification of the recombinant polypeptide by acting as a ligand during purification.
  • a proteolytic cleavage site is introduced at the junction of the fusion moiety and the recombinant polypeptide to enable separation of the recombinant polypeptide from the fusion moiety after purification of the fusion polypeptide.
  • enzymes, and their cognate recognition sequences include Factor Xa, thrombin and enterokinase.
  • Typical fusion expression vectors include pGEX (Pharmacia Biotech Inc; (Smith & Johnson, 1988)), pMAL (New England Biolabs, Beverly, Mass.) and pRIT5 (Pharmacia, Piscataway, NJ.) which fuse glutathione S- transferase (GST), maltose E binding polypeptide, or polypeptide A, respectively, to the target recombinant polypeptide.
  • GST glutathione S- transferase
  • maltose E binding polypeptide or polypeptide A, respectively, to the target recombinant polypeptide.
  • fusion polypeptides can be used in screening assays and to generate antibodies specific for polypeptides.
  • fusion polypeptide expressed in a retroviral expression vector can be used to infect bone marrow cells that are subsequently transplanted into irradiated recipients. The pathology of the subject recipient is then examined after sufficient time has passed.
  • a polypeptide in host bacteria with an impaired capacity to proteolytically cleave the recombinant polypeptide can be used to maximize recombinant polypeptide expression (Gottesman, 1990).
  • the nucleotide sequence of the nucleic acid to be inserted into an expression vector can be changed so that the individual codons for each amino acid are those preferentially utilized in E. coli (Wada et al., 1992).
  • the expression vector's control functions are often provided by viral regulatory elements.
  • promoters are derived from polyoma, Adenovirus 2, cytomegalovirus and Simian Virus 40.
  • Recombinant mammalian expression vectors can be capable of directing expression of the nucleic acid in a particular cell type (e.g., tissue-specific regulatory elements are used to express the nucleic acid).
  • tissue-specific promoters include an albumin promoter (Pinkert et al., 1987), lymphoid-specif ⁇ c promoters (Calame and Eaton, 1988) , promoters of immunoglobulins (Banerji et al.
  • a nucleic acid from one of the tables might be cloned into an expression vector in an antisense orientation.
  • Regulatory sequences e.g., viral promoters and/or enhancers
  • operatively linked to a nucleic acid cloned in the antisense orientation can be chosen for directing constitutive, tissue specific or cell type specific expression of antisense RNA in a variety of cell types.
  • Antisense expression vectors can be in the form of a recombinant plasmid, phagemid or attenuated virus.
  • the invention includes host cells having a nucleotide sequence from the tables within a recombinant expression vector or a fragment of such a sequence, which facilitate homologous recombination into a specific site of the host cell genome.
  • Terms such as host cell and recombinant host cell refer not only to the particular subject cell but also to the progeny of a cell. Because certain modifications may occur in succeeding generations due to either mutation or environmental influences, such progeny may not, in fact, be identical to the parent cell.
  • a host cell can be any prokaryotic or eukaryotic cell.
  • a polypeptide can be expressed in bacterial cells such as E, coli, insect cells, yeast or mammalian cells (such as Chinese hamster ovary cells (CHO) or COS cells).
  • Vectors can be introduced into host cells via conventional transformation or transfection techniques.
  • transformation and transfection refer to a variety of techniques known for introducing foreign nucleic acid (e.g., DNA) into a host cell, including calcium phosphate or calcium chloride co-precipitation 3 transduction/infection, DEAE-dextran-mediated transfection, lipofection, or electroporation.
  • a host cell can be used to produce a polypeptide. Accordingly, methods for producing a polypeptide using the host cells are included as part of this invention. Such a method can include culturing host cells into which a recombinant expression vector encoding a polypeptide has been introduced in a suitable medium such that the polypeptide is produced. The method can further include isolating the polypeptide from the medium or the host cell.
  • the invention also includes cells or purified preparations of cells which include a transgene from the tables, or which otherwise mis-express a polypeptide.
  • Cell preparations can consist of human or non-human cells, e.g., rodent cells, e.g., mouse or rat cells, rabbit cells, or pig cells.
  • the transgene can be mis-expressed, e.g., over-expressed or under-expressed.
  • the cell or cells include a gene which misexpresses an endogenous polypeptide (e.g., expression of a gene is disrupted, also known as a knockout).
  • Such cells can serve as a model for studying disorders which are related to mutated or mis-expressed alleles or for use in drug screening.
  • human cells e.g., hematopoietic stem cells transformed with a nucleic acid from the tables.
  • the invention includes cells or a purified preparation thereof (e.g., human cells) in which an endogenous nucleic acid from the tables is under the control of a regulatory sequence that does not normally control the expression of the endogenous gene corresponding to the sequence.
  • a regulatory sequence that does not normally control the expression of the endogenous gene corresponding to the sequence.
  • the expression characteristics of an endogenous gene within a cell can be modified by inserting a heterologous DNA regulatory element into the genome of the cell such that the inserted regulatory element is operably linked to the corresponding endogenous gene.
  • an endogenous corresponding gene e.g., a gene which is transcriptionally silent, not normally expressed, or expressed only at very low levels
  • a regulatory element which is capable of promoting the expression of a normally expressed gene product in that cell.
  • Techniques such as targeted homologous recombinations, can be used to insert the heterologous DNA as described in, e.g., Chappel, U.S. Pat. No. 5,272,071; WO 91/06667, published on May 16, 1991.
  • Non-human transgenic animals that express a heterologous polypeptide e.g., expressed from a nucleic acid from the tables) can be generated.
  • a transgenic animal is a non-human animal such as a mammal (e.g., a non-human primate such as chimpanzee, baboon, or macaque; an ungulate such as an equine, bovine, or caprine; or a rodent such as a rat, a mouse, or an Israeli sand rat), a bird (e.g., a chicken or a turkey), an amphibian (e.g., a frog, salamander, or newt), or an insect (e.g., Drosophila melanogaster), in which one or more of the cells of the animal includes a transgene.
  • a mammal e.g., a non-human primate such as chimpanzee, baboon, or macaque
  • an ungulate such as an equine, bovine, or caprine
  • a rodent such as a rat, a mouse, or an Israeli sand rat
  • a transgene is exogenous DNA or a rearrangement (e.g., a deletion of endogenous chromosomal DNA) that is often integrated into or occurs in the genome of cells in a transgenic animal.
  • a transgene can direct expression of an encoded gene product in one or more cell types or tissues of the transgenic animal.
  • a transgenic animal can be one in which an endogenous nucleic acid homologous to a nucleic acid from the tables has been altered by homologous recombination between the endogenous gene and an exogenous DNA molecule introduced into a cell of the animal (e.g., an embryonic cell of the animal) prior to development of the animal.
  • Intronic sequences and polyadenylation signals can also be included in the transgene to increase expression efficiency of the transgene.
  • One or more tissue-specific regulatory sequences can be operably linked to a nucleotide sequence from the tables to direct expression of an encoded polypeptide to particular cells.
  • a transgenic founder animal can be identified based upon the presence of the nucleotide sequence in its genome and/or expression of encoded mRNA in tissues or cells of the animals. A transgenic founder animal can then be used to breed additional animals carrying the transgene.
  • transgenic animals carrying a nucleotide sequence can further be bred to other transgenic animals carrying other transgenes.
  • Polypeptides can be expressed in transgenic animals or plants by introducing a nucleic acid encoding the polypeptide into the genome of an animal.
  • the nucleic acid is placed under the control of a tissue specific promoter, e.g., a milk or egg specific promoter s and recovered from the milk or eggs produced by the animal.
  • a population of cells from a transgenic animal is also included.
  • polypeptide or protein is substantially free of cellular material or other contaminating proteins from the cell or tissue source from which the protein is derived, or is substantially free from chemical precursors or other chemicals when chemically synthesized.
  • substantially free means a preparation of a polypeptide having less than about 5% (by dry weight) of contaminating protein, or of chemical precursors or non-target chemicals.
  • the desired polypeptide is recombinantly produced, it is typically substantially free of culture medium, specifically, where culture medium represents less than about 10% of the polypeptide preparation.
  • polypeptides may exist as chimeric or fusion polypeptides.
  • a "target chimeric polypeptide” or “target fusion polypeptide” includes a target polypeptide linked to a different polypeptide.
  • the target polypeptide in the fusion polypeptide can correspond to an entire or nearly entire polypeptide as it exists in nature or a fragment thereof.
  • the other polypeptide can be fused to the N-terminus or C-terminus of the target polypeptide.
  • Fusion polypeptides can include a moiety having high affinity for a ligand.
  • the fusion polypeptide can be a GST-target fusion polypeptide in which the target sequences are fused to the C-terminus of the GST sequences, or a polyhistidine-target fusion polypeptide in which the target polypeptide is fused at the N- or C-terminus to a string of histidine residues.
  • Such fusion polypeptides can facilitate purification of recombinant target polypeptide.
  • Fusion moiety e.g., a GST polypeptide
  • a nucleotide sequence from the tables, or a substantially identical nucleotide sequence thereof can be cloned into an expression vector such that the fusion moiety is linked in-frame to the target polypeptide.
  • the fusion polypeptide can be a target polypeptide containing a heterologous signal sequence at its N-terminus.
  • expression, secretion, cellular internalization, and cellular localization of a target polypeptide can be increased through use of a heterologous signal sequence.
  • Fusion polypeptides can also include all or a part of a serum polypeptide (e.g., an IgG constant region or human serum albumin).
  • Target polypeptides can be incorporated into pharmaceutical compositions and administered to a subject in vivo. Administration of these polypeptides can be used to affect the bioavailability of a substrate of the polypeptide and may effectively increase polypeptide biological activity in a cell.
  • Target fusion polypeptides may be useful therapeutically for the treatment of disorders caused by, for example, (i) aberrant modification or mutation of a gene encoding a polypeptide; (ii) mis-regulation of the gene encoding the polypeptide; and (iii) aberrant post-translational modification of a polypeptide.
  • target polypeptides can. be used as immunogens to produce anti-target antibodies in a subject, to purify the polypeptide ligands or binding partners, and in screening assays to identify molecules which inhibit or enhance the interaction of a polypeptide with a substrate.
  • Polypeptides can be differentially modified during or after translation, e.g., by glycosylation, acetylation, phosphorylation, amidation, derivatization by known protecting/blocking groups, proteolytic cleavage, linkage to an antibody molecule or other cellular ligand, etc. Any known modification including specific chemical cleavage by cyanogen bromide, trypsin, chymotrypsin, papain, V8 protease, NaBH 4 ; acetylation, formylation, oxidation, reduction; metabolic synthesis in the presence of tunicamycin; etc. may be used.
  • Additional post- translational modifications include, for example, N-linked or O-linked carbohydrate chains, processing of N-terminal or C-terminal ends), attachment of chemical moieties to the amino acid backbone, chemical modifications of N-linked or O-linked carbohydrate chains, and addition or deletion of an N-terminal methionine residue as a result of prokaryotic host cell expression.
  • the polypeptide fragments may also be modified with a detectable label, such as an enzymatic, fluorescent, isotopic or affinity label to allow for detection and isolation of the polypeptide.
  • Chemically modified derivatives of polypeptides that can provide additional advantages such as increased solubility, stability and circulating time of the polypeptide, or decreased immunogenicity (see e.g., U.S. Pat. No. 4,179,337) are also part of this invention.
  • the chemical moieties for derivitization may be selected from water soluble polymers such as polyethylene glycol, ethylene glycol/propylene glycol copolymers, carboxymethylcellulose, dextran, polyvinyl alcohol and the like.
  • the polypeptides may be modified at random positions within the molecule, or at predetermined positions within the molecule and may include one, two, three or more attached chemical moieties.
  • the polymer may be of any molecular weight, and may be branched or unbranched.
  • the molecular weight often is between about 1 kDa and about 100 kDa for ease in handling and manufacturing. Other sizes may be used, depending on the desired therapeutic profile (e.g., the duration of sustained release desired, the effects, if any on biological activity, the ease in handling, the degree or lack of antigenicity and other known effects of the polyethylene glycol to a therapeutic protein or analog).
  • polymers can be attached to the polypeptide with consideration of effects on functional or antigenic domains of the polypeptide.
  • attachment methods available to those skilled in the art (e.g., EP 0 401 384 (coupling PEG to G-CSF) and Malik et al (Malik et al, 1992)
  • polyethylene glycol may be covalently bound through amino acid residues via a reactive group, such as a free amino or carboxyl group.
  • Reactive groups are those to which an activated polyethylene glycol molecule may be bound.
  • the amino acid residues having a free amino group may include lysine residues and the N- terminal amino acid residues; those having a free carboxyl group may include aspartic acid residues, glutamic acid residues and the C-terminal amino acid residue.
  • Sulfhydryl groups may also be used as a reactive group for attaching the polyethylene glycol molecules.
  • the attachment sometimes is at an amino group, such as attachment at the N-terminus or lysine group.
  • Proteins can be chemically modified at the N-terminus.
  • polyethylene glycol for example, one may select from a variety of polyethylene glycol molecules (by molecular weight, branching, and the like), the proportion of polyethylene glycol molecules to protein (polypeptide) molecules in the reaction mix, the type of pegylation reaction to be performed, and the method of obtaining the selected N-terminally pegylated protein.
  • the method of obtaining the N-terminally pegylated preparation i.e., separating this moiety from other monopegylated moieties if necessary
  • Selective proteins chemically modified at the N-terminus may be accomplished by reductive alkylation, which exploits differential reactivity of different types of primary amino groups (lysine versus the N- terminal) available for derivatization in a particular protein. Under the appropriate reaction conditions, substantially selective derivatization of the protein at the N-terminus with a carbonyl group containing polymer is achievable.
  • Pharmacogenomics is a discipline that involves tailoring a treatment for a subject according to the subject's genotype. For example, based upon the outcome of a prognostic test, a clinician or physician may target pertinent information and preventative or therapeutic treatments to a subject who would be benefited by the information or treatment and avoid directing such information and treatments to a subject who would not be benefited (e.g., the treatment has no therapeutic effect and/or the subject experiences adverse side effects). As therapeutic approaches for colorectal cancer continue to evolve and improve, the goal of treatments for colorectal cancer related disorders is to intervene even before clinical signs manifest themselves. Thus, genetic markers associated with susceptibility to colorectal cancer prove useful for early diagnosis, prevention and treatment of colorectal cancer.
  • a particular treatment regimen can exert a differential effect depending upon the subject's genotype.
  • a candidate therapeutic exhibits a significant beneficial interaction with a prevalent allele and a comparatively weak interaction with an uncommon allele (e.g., an order of magnitude or greater difference in the interaction)
  • such a therapeutic typically would not be administered to a subject genotyped as being homozygous for the uncommon allele, and sometimes not administered to a subject genotyped as being heterozygous for the uncommon allele.
  • a candidate therapeutic is not significantly toxic when administered to subjects who are homozygous for a prevalent allele but is comparatively toxic when administered to subjects heterozygous or homozygous for an uncommon allele
  • the candidate therapeutic is not typically administered to subjects who are genotyped as being heterozygous or homozygous with respect to the uncommon allele.
  • Methods of the invention are applicable to pharmacogenomic methods for detecting, preventing, alleviating and/or treating colorectal cancer.
  • a nucleic acid sample from an individual may be subjected to a genetic test. Where one or more SNPs associated with increased risk of colorectal cancer are identified in a subject, information for detecting, preventing or treating colorectal cancer and/or one or more colorectal cancer detection, prevention and/or treatment regimens then may be directed to and/or prescribed to that subject.
  • a detection, preventative and/or treatment regimen is specifically prescribed and/or administered to individuals who will most benefit from it based upon their risk of developing colorectal cancer assessed by the methods described herein.
  • Certain embodiments are directed to methods for treating colorectal cancer in a subject, reducing risk of colorectal cancer in a subject, or early detection of colorectal cancer in a subject, which comprise: detecting the presence or absence of a SNP associated with colorectal cancer in a nucleotide sequence set forth in SEQ ID NOs: 1 to 268, and prescribing or administering a colorectal cancer treatment regimen, preventative regimen and/or detection regimen to a subject from whom the sample originated where the presence of one or more SNPs associated with colorectal cancer are detected in the nucleotide sequence.
  • genetic results may be utilized in combination with other test results to diagnose colorectal cancer as described above.
  • colorectal cancer treatments include surgery, chemotherapy and/or radiation therapy. Any of the treatments may be used subsequently or in combination to treat or prevent colorectal cancer (e.g., surgery followed by radiation therapy or chemotherapy).
  • Pharmacogenomic methods also may be used to analyze and predict a response to a colorectal cancer treatment or a drug. For example, if pharmacogenomic analysis indicates a likelihood that an individual will respond positively to a colorectal cancer treatment with a particular drug, the drug may be administered to the individual. Conversely, if the analysis indicates that an individual is likely to respond negatively to treatment with a particular drug, an alternative course of treatment may be prescribed. A negative response may be defined as either the absence of an efficacious response or the presence of toxic side effects.
  • the response to a therapeutic treatment can be predicted in a background study in which subjects in any of the following populations are genotyped: a population that responds favorably to a treatment regimen, a population that does not respond significantly to a treatment regimen, and a population that responds adversely to a treatment regiment (e.g., exhibits one or more side effects). These populations are provided as examples and other populations and subpopulations may be analyzed. Based upon the results of these analyses, a subject is genotyped to predict whether he or she will respond favorably to a treatment regimen, not respond significantly to a treatment regimen, or respond adversely to a treatment regimen.
  • the methods described herein also are applicable to clinical drug trials.
  • One or more SNPs indicative of response to an agent for treating colorectal cancer or to side effects to an agent for treating colorectal cancer may be identified. Thereafter, potential participants in clinical trials of such an agent may be screened to identify those individuals most likely to respond favorably to the drug and exclude those likely to experience side effects. In that way, the effectiveness of drug treatment may be measured in individuals who respond positively to the drug, without lowering the measurement as a result of the inclusion of individuals who are unlikely to respond positively in the study and without risking undesirable safety problems.
  • another embodiment is a method of selecting an individual for inclusion in a clinical trial of a treatment or drug comprising the steps of: (a) obtaining a nucleic acid sample from an individual; (b) determining the identity of a polymorphic variant, e.g., SNP which is associated with a positive response to the treatment or the drug, or at least one SNP which is associated with a negative response to the treatment or the drug in the nucleic acid sample, and (c) including the individual in the clinical trial if the nucleic acid sample contains the SNP associated with a positive response to the treatment or the drug or if the nucleic acid sample lacks said SNP associated with a negative response to the treatment or the drug.
  • a polymorphic variant e.g., SNP which is associated with a positive response to the treatment or the drug, or at least one SNP which is associated with a negative response to the treatment or the drug in the nucleic acid sample
  • Step (c) can also include administering the drug or the treatment to the individual if the nucleic acid sample contains the SNP associated with a positive response to the treatment or the drug and the nucleic acid sample lacks the SNP associated with a negative response to the treatment or the drug.
  • compositions Comprising Colorectal Cancer-Directed Molecules
  • the invention includes a composition made up of a colorectal cancer cell and one or more molecules specifically directed and targeted to a nucleic acid comprising a nucleotide sequence shown in the tables, or a polypeptide encoded thereby.
  • Such directed molecules include, but are not limited to, a compound that binds to a nucleic acid or a polypeptide; a RNAi or siRNA molecule having a strand complementary to a nucleotide sequence; an antisense nucleic acid complementary to an RNA encoded by a DNA sequence; a ribozyme that hybridizes to a nucleotide sequence; a nucleic acid aptamer that specifically binds a polypeptide; and an antibody that specifically binds to a polypeptide or binds to a nucleic acid.
  • the colorectal cancer directed molecule interacts with a nucleic acid or polypeptide variant associated with colorectal cancer.
  • Compounds can be obtained using any of numerous approaches in combinatorial library methods known in the art, including: biological libraries; peptoid libraries (libraries of molecules having the functionalities of peptides, but with a novel, non-peptide backbone which are resistant to enzymatic degradation but which nevertheless remain bioactive (Zuckermann et al, 1994).
  • Biological library and peptoid library approaches are typically limited to peptide libraries, while the other approaches are applicable to peptide, non-peptide oligomer or small molecule libraries of compounds (Lam, 1997). Examples of methods for synthesizing molecular libraries are described, for example, in DeWitt et al. (DeWitt et al.
  • Libraries of compounds may be presented in solution (Houghten et al, 1992), or on beads (Lam et al, 1991), chips (Fodor et al, 1993), bacteria or spores (Ladner, U.S. Pat. No. 5,223,409), plasmids (Cull et al, 1992) or on phage (Scott and Smith, 1990; Devlin et al, 1990; CwMa et al, 1990; Felici et al, 1991).
  • Small molecules include peptides, peptidomimetics (e.g., peptoids), amino acids, amino acid analogs, polynucleotides, polynucleotide analogs, nucleotides, nucleotide analogs, organic or inorganic compounds (i.e., including heteroorganic and organometallic compounds) having a molecular weight less than about 10,000 grams per mole, organic or inorganic compounds having a molecular weight less than about 5,000 grams per mole, organic or inorganic compounds having a molecular weight less than about 1,000 grams per mole, organic or inorganic compounds having a molecular weight less than about 500 grams per mole, and salts, esters, and other pharmaceutically acceptable forms of such compounds.
  • peptides e.g., peptoids
  • amino acids amino acid analogs
  • polynucleotides polynucleo
  • An antisense nucleic acid refers to a nucleotide sequence complementary to a sense nucleic acid encoding a polypeptide, e.g., complementary to the, coding strand of a double-stranded cDNA molecule or complementary to an mRNA sequence.
  • the antisense nucleic acid can be complementary to an entire coding strand in a nucleic acid molecule having a sequence of one of SEQ ID NOs:261 to 268, or to a portion thereof.
  • the antisense nucleic acid molecule is antisense to a non-coding region of the coding strand of a nucleotide sequence, e.g., 5' and 3 V untranslated regions.
  • An antisense nucleic acid can be designed such that it is complementary to the entire coding region of an mRNA encoded by a nucleotide sequence of interest, and often the antisense nucleic acid is an oligonucleotide antisense to only a portion of a coding or non-coding region of the mRNA.
  • the antisense oligonucleotide can be complementary to the region surrounding the translation start site of the mRNA, e.g., between the -10 and +10 regions of the target gene nucleotide (SNP) sequence of interest.
  • SNP target gene nucleotide
  • An antisense oligonucleotide can be, for example, about 7, 10, 15, 20, 25, 30, 35, 4O 3 45, 50, 55, 60, 65, 70, 75, 80, or more nucleotides in length.
  • the antisense nucleic acids which include the ribozymes described below, can be designed to target a nucleotide sequence in any of SEQ ID NOs:261 to 268. Uncommon alleles and prevalent alleles can be targeted, and those associated with an increased risk of colorectal cancer are often designed, tested, and administered to subjects,
  • An antisense nucleic acid can be constructed using chemical synthesis and enzymatic ligation reactions using standard procedures.
  • an antisense nucleic acid molecule can be chemically synthesized using naturally occurring nucleotides or variously modified nucleotides designed to increase the biological stability of the molecules or to increase the physical stability of the duplex formed between the antisense and sense nucleic acids, e.g., phosphorothioate derivatives and acridine substituted nucleotides can be used.
  • Antisense nucleic acid also can be produced biologically using an expression vector into which a nucleic acid has been subcloned in an antisense orientation (i.e., RNA transcribed from the inserted nucleic acid will be of an antisense orientation to a target nucleic acid of interest.
  • an antisense orientation i.e., RNA transcribed from the inserted nucleic acid will be of an antisense orientation to a target nucleic acid of interest.
  • antisense nucleic acids When utilized as therapeutics, antisense nucleic acids typically are administered to a subject (e.g., by direct injection at a tissue site) or generated in situ such that they hybridize with or bind to cellular mRNA and/or genomic DNA encoding a polypeptide and thereby inhibit expression of the polypeptide, for example, by inhibiting transcription and/or translation.
  • antisense nucleic acid molecules can be modified to target selected cells and then are administered systemically.
  • antisense molecules can be modified such that they specifically bind to receptors or antigens expressed on a selected cell surface, for example, by linking antisense nucleic acid molecules to peptides or antibodies which bind to cell surface receptors or antigens.
  • Antisense nucleic acid molecules can also be delivered to cells using vectors. Sufficient intracellular concentrations of antisense molecules are achieved by incorporating a strong promoter, such as a pol II or pol III promoter, in the vector construct.
  • Antisense nucleic acid molecules sometimes are anomeric nucleic acid molecules (Gautier et al. , 1987). Antisense nucleic acid molecules can also comprise a 2 r -o-methylribonucleotide (Inoue el al, 1987a) or a chimeric RNA-DNA analogue (Inoue et al, 1987b). Antisense nucleic acids sometimes are composed of DNA or peptide nucleic acid (PNA).
  • PNA peptide nucleic acid
  • an antisense nucleic acid is a ribozyme.
  • a ribozyme having specificity for a target nucleotide sequence can include one or more sequences complementary to such a nucleotide sequence, and a sequence having a known catalytic region responsible for mRNA cleavage (see e.g., U.S. Pat. No. 5,093,246 or Haselhoff and Gerlach (Haseloff and Gerlach, 1988).
  • a derivative of a Tetrahymena L-19 IVS RNA is sometimes utilized in which the nucleotide sequence of the active site is complementary to the nucleotide sequence to be cleaved in a mRNA (see e.g., Cech et al, U.S. Pat. No. 4,987,071; and Cech et al, U.S. Pat. No. 5,116,742).
  • target mRNA sequences can be used to select a catalytic RNA having a specific ribonuclease activity from a pool of RNA molecules (Bartel and Szostak, 1993).
  • Colorectal cancer directed molecules include in certain embodiments nucleic acids that can form triple helix structures with a target nucleotide sequence, especially one that includes a regulatory region that controls expression of a polypeptide.
  • Gene expression can be inhibited by targeting nucleotide sequences complementary to the regulatory region of a target nucleotide sequence (e.g., promoter and/or enhancers) to form triple helical structures that prevent transcription of a gene in target cells (Helene, 1991; Helene et al, 1992; Maher, III, 1992).
  • Potential sequences that can be targeted for triple helix formation can be increased by creating a switchback nucleic acid molecule.
  • Switchback molecules are synthesized in an alternating 5'-3' s 3'-5 r manner, such that they base pair with first one strand of a duplex and then the other, eliminating the necessity for a sizeable stretch of either purines or pyrimidines to be present on one strand of a duplex.
  • Colorectal cancer directed molecules include RNAi and siRNA nucleic acids. Gene expression may be inhibited by the introduction of double-stranded RNA (dsRNA), which induces potent and specific gene silencing, a phenomenon called RNA interference or RNAi.
  • dsRNA double-stranded RNA
  • RNAi RNA interference
  • Fire et al U.S. Pat. No. 6,506,559
  • Tuschl et al PCT International Publication No, WO 01/75164
  • Kay et al PCT International Publication No. WO 03/010180A1
  • Bosher J M Labouesse (Bosher and Labouesse, 2000).
  • RNA interference RNA interference
  • siRNA or RNAi is a nucleic acid that forms a double stranded RNA and has the ability to reduce or inhibit expression of a gene or target gene when the siRNA is delivered to or expressed in the same cell as the gene or target gene.
  • siRNA is short double-stranded RNA formed by the complementary strands. Complementary portions of the siRNA that hybridize to form the double stranded molecule often have substantial or complete identity to the target molecule sequence.
  • an siRNA is a nucleic acid that has substantial or complete identity to a target gene and forms a double stranded siRNA.
  • the targeted region When designing the siRNA molecules, the targeted region often is selected from a given DNA sequence beginning 50 to 100 nucleotides downstream of the start codon. See, e.g., Elbashir et al (Elbashir et al, 2002). Initially, 5 ' or 3' UTRs and regions nearby the start codon were avoided assuming that UTR-binding proteins and/or translation initiation complexes may interfere with binding of the siRNP or RISC endonuclease complex. Sometimes regions of the target 23 nucleotides in length conforming to the sequence motif AA (N19)TT (N, an nucleotide), and regions with approximately 30% to 70% G/C-content (often about 50% G/C-content) often are selected.
  • the search often is extended using the motif NA (N2 1).
  • the sequence of the sense siRNA sometimes corresponds to (N 19) TT orN21 (position 3 to 23 of the 23-nt motif), respectively. In the latter case, the 3' end of the sense siRNA often is converted to TT.
  • the rationale for this sequence conversion is to generate a symmetric duplex with respect to the sequence composition of the sense and antisense 3' overhangs.
  • the antisense siRNA is synthesized as the complement to position 1 to 21 of the 23-nt motif. Because position 1 of the 23-nt motif is not recognized sequence-specifically by the antisense siRNA, the 3'-most nucleotide residue of the antisense siRNA can be chosen deliberately.
  • the penultimate nucleotide of the antisense siRNA (complementary to position 2 of the 23-nt motif) often is complementary to the targeted sequence.
  • TT often is utilized.
  • Respective 21 nucleotide sense and antisense siRNAs often begin with a purine nucleotide and can also be expressed from pol III expression vectors without a change in targeting site. Expression of RNAs from pol III promoters can be more efficient when the first transcribed nucleotide is a purine.
  • the sequence of the siRNA can correspond to the full length target gene, or a subsequence thereof.
  • the siRNA is about 15 to about 50 nucleotides in length (e.g., each complementary sequence of the double stranded siRNA is 15 to 50 nucleotides in length, and the double stranded siRNA is about 15 to 50 base pairs in length, sometimes about 20 to 30 nucleotides in length or about 20 to 25 nucleotides in length, e.g., 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, or 30 nucleotides in length.
  • the siRNA sometimes is about 21 nucleotides in length.
  • Antisense, ribozyme, RNAi and siRNA nucleic acids can be altered to form modified nucleic acid molecules.
  • the nucleic acids can be altered at base moieties, sugar moieties or phosphate backbone moieties to improve stability, hybridization, or solubility of the molecule.
  • the deoxyribose phosphate backbone of nucleic acid molecules can be modified to generate peptide nucleic acids (see Hyrup et al, Bioorganic & Medicinal Chemistry 4 (1): 5- 23 (1996)).
  • a peptide nucleic acid, or PNA refers to a nucleic acid mimic such as a DNA mimic, in which the deoxyribose phosphate backbone is replaced by a pseudopeptide backbone and only the four natural nucleobases are retained.
  • the neutral backbone of a PNA can allow for specific hybridization to DNA and RNA under conditions of low ionic strength. Synthesis of PNA oligomers can be performed using standard solid phase peptide synthesis protocols as described, for example, in Hyrup et al. (Hyrup and Nielsen, 1996), and Perry- O'Keefe et al. (Abderrahmani et al , 2001 ).
  • PNA nucleic acids can be used in prognostic, diagnostic, and therapeutic applications.
  • PNAs can be used as anti-sense or anti-gene agents for sequence-specific modulation of gene expression by, for example, inducing transcription or translation arrest or inhibiting replication
  • PNA nucleic acid molecules can also be used in the analysis of SNPs in a gene, (e.g., by PNA-directed PCR clamping); as artificial restriction enzymes when used in combination with other enzymes, (e.g., Sl nucleases (Hyrup and Nielsen, 1996) or as probes or primers for DNA sequencing or hybridization (Hyrup and Nielsen, 1996; Perry-O'Keefe et #/., 1996).
  • oligonucleotides may include other appended groups such as peptides (e.g., for targeting host cell receptors in vivo), or agents facilitating transport across cell membranes (see e.g., Letsinger et al. (Letsinger et al, 1989); Lemaitre et al (Lemaitre et al, 1987) and PCT Publication No. W088/09810) or the blood-brain barrier (see, e.g., PCT Publication No. W089/10134).
  • oligonucleotides can be modified with hybridization-triggered cleavage agents (van der Krol et al, 1988) or intercalating agents (Zon, 1988).
  • the oligonucleotide may be conjugated to another molecule, (e.g., a peptide, hybridization triggered cross-linking agent, transport agent, or hybridization- triggered cleavage agent).
  • molecular beacon oligonucleotide primer and probe molecules having one or more regions complementary to a target nucleotide sequence, two complementary regions one having a fluorophore and one a quencher such that the molecular beacon is useful for quantifying the presence of the nucleic acid in a sample.
  • Molecular beacon nucleic acids are described, for example, in Lizardi et al, U.S. Pat. No. 5,854,033; Nazarenko et al, U.S. Pat. No. 5,866,336, and Uvak et aL , U.S. Pat. No. 5,876,930.
  • Antibodies are described, for example, in Lizardi et al, U.S. Pat. No. 5,854,033; Nazarenko et al, U.S. Pat. No. 5,866,336, and Uvak et aL , U.S. Pat. No. 5,876,930.
  • An immunogen typically is used to prepare antibodies by immunizing a suitable subject, (e.g., rabbit, goat, mouse or other mammal).
  • An appropriate immunogenic preparation can contain, for example, recombinantly expressed chemically synthesized polypeptide.
  • the preparation can further include an adjuvant, such as Freund's complete or incomplete adjuvant, or a similar immunostimulatory agent.
  • Amino acid polymorphisms can be detected using antibodies specific for the altered epitope by western analysis after the electrophoresis of denatured proteins. Protein polymorphism can also be detected using fluorescently identified antibodies which bind to specific polymorphic epitopes and detected in whole cells using fluorescence activated cell sorting techniques (FACS). Polymorphic protein sequence may also be determined by NMR spectroscopy or by x-ray diffraction studies. Further, determination of polymorphic sites in proteins may be accomplished by observing differential cleavage by specific or non specific proteases.
  • An antibody is an immunoglobulin molecule or immunologically active portion thereof, i.e., an antigen-binding portion.
  • immunologically active portions of immunoglobulin molecules include F(ab) and F(ab') 2 fragments which can be generated by treating the antibody with an enzyme such as pepsin.
  • An antibody can be polyclonal, monoclonal, or recombinant (e.g., a chimeric or humanized), fully human, non-human (e.g., murine), or a single chain antibody.
  • An antibody may have effector function and can fix complement, and is sometimes coupled to a toxin or imaging agent.
  • a full-length polypeptide or antigenic peptide fragment encoded by a target nucleotide sequence can be used as an immunogen or can be used to identify antibodies made with other immunogens, e.g., cells, membrane preparations, and the like.
  • An antigenic peptide often includes at least 8 amino acid residues of the amino acid sequences encoded by a nucleotide sequence of one of SEQ ID NOs:261 to 268, and encompasses an epitope.
  • Antigenic peptides sometimes include 10 or more amino acids, 15 or more amino acids, 20 or more amino acids, or 30 or more amino acids. Hydrophilic and hydrophobic fragments of polypeptides sometimes are used as immunogens.
  • Epitopes encompassed by the antigenic peptide are regions located on the surface of the polypeptide (e.g., hydrophilic regions) as well as regions with high antigenicity.
  • regions located on the surface of the polypeptide e.g., hydrophilic regions
  • an Eraini surface probability analysis of the human polypeptide sequence can be used to indicate the regions that have a particularly high probability of being localized to the surface of the polypeptide and are thus likely to constitute surface residues useful for targeting antibody production.
  • the antibody may bind an epitope on any domain or region on polypeptides for use in the invention.
  • Chimeric, humanized, and completely human antibodies are useful for applications which include repeated administration to subjects.
  • Chimeric and humanized monoclonal antibodies comprising both human and non-human portions, can be made using standard recombinant DNA techniques.
  • Such chimeric and humanized monoclonal antibodies can be produced by recombinant DNA techniques, for example using methods described in
  • Completely human antibodies can be particularly desirable for therapeutic treatment of human patients.
  • Such antibodies can be produced using transgenic mice that are incapable of expressing endogenous immunoglobulin heavy and light chains genes, but which can express human heavy and light chain genes. See, for example, Lonberg and Huszar (Lonberg and Huszar, 1995) and U.S. Pat. Nos. 5,625,126; 5,633,425; 5,569,825; 5,661,016; and 5,545,806.
  • companies such as Abgenix, Inc. (Fremont, Calif.) and Medarex, Inc. (Princeton, N.J.), can be engaged to provide human antibodies directed against a selected antigen.
  • Completely human antibodies that recognize a selected epitope also can be generated using guided selection, In this approach a selected non-human monoclonal antibody (e.g., a murine antibody) is used to guide the selection of a completely human antibody recognizing the same epitope.
  • a selected non-human monoclonal antibody e.g., a murine antibody
  • Jespers et al Jespers et al. , 1994.
  • An antibody can be a single chain antibody.
  • a single chain antibody (scFV) can be engineered (see, e.g., Colcher et al (Colcher et al, 1999) and Reiter (Reiter and Pastan, 1996).
  • Single chain antibodies can be dimerized or multimerized to generate multivalent antibodies having specificities for different epitopes of the same target polypeptide.
  • Antibodies also may be selected or modified so that they exhibit reduced or no ability to bind an Fc receptor.
  • an antibody may be an isotype or subtype, fragment or other mutant, which does not support binding to an Fc receptor (e.g., it has a mutagenized or deleted Fc receptor binding region).
  • an antibody may be conjugated to a therapeutic moiety such as a cytotoxin, a therapeutic agent or a radioactive metal ion.
  • a cytotoxin or cytotoxic agent includes any agent that is detrimental to cells. Examples include taxol, cytochalasin B, gramicidin D, ethidium bromide, emetine, mitomycin, etoposide, tenoposide, vincristine, vinblastine, colchicin, doxorubicin, daunorubicin, dihydroxy anthracin dione, mitoxantrone, mithramycin, actinomycin D, 1 dehydrotestosterone, glucocorticoids, procaine, tetracaine, lidocaine, propranolol, and puromycin and analogs or homologs thereof.
  • Therapeutic agents include antimetabolites (e.g., methotrexate, 6-mercaptopurine, 6-thioguanine, cytarabine, 5- fluorouracil decarbazine), alkylating agents (e.g., mechlorethamine, thiotepa chlorambucil, melphalan, carmustine (BCNU) and lomustine (CCNU), cyclophosphamide, busulfan, dibromomannitol, streptozotocin, mitomycin C, and cis-dichlorodiamine platinum (II) (DDP) cisplatin), anthracyclines (e.g., daunorubicin (formerly daunomycin) and doxorubicin), antibiotics (e.g., dactinomycin (formerly actinomycin), bleomycin, mithramycin, and anthramycin (AMC)), and anti-mitotic agents (e.g., vincristine and
  • Antibody conjugates can be used for modifying a given biological response.
  • the drug moiety may be a protein or polypeptide possessing a desired biological activity.
  • proteins may include, for example, a toxin such as abrin, ricin A, pseudomonas exotoxin, or diphtheria toxin; a polypeptide such as tumor necrosis factor, ⁇ -interferon, ⁇ - interferon, nerve growth factor, platelet derived growth factor, tissue plasminogen activator; or, biological response modifiers such as, for example, lymphokines, interleukin-1 ("IL-I”), interleukin-2 (“IL-2”), interleukin-6 (“IL-6”), granulocyte macrophage colony stimulating factor (“GM- CSF”), granulocyte colony stimulating factor (“G-CSF”), or other growth factors.
  • IL-I interleukin-1
  • IL-2 interleukin-2
  • IL-6 interleukin-6
  • GM- CSF gran
  • an antibody can be conjugated to a second antibody to form an antibody hetero conjugate as described by Segal in U.S. Pat. No. 4,676,980, for example.
  • An antibody e.g., monoclonal antibody
  • An antibody can be used to isolate target polypeptides by standard techniques, such as affinity chromatography or irnmunoprecipitation.
  • an antibody can be used to detect a target polypeptide (e.g., in a cellular lysate or cell supernatant) in order to evaluate the abundance and pattern of expression of the polypeptide.
  • Antibodies can be used diagnostically to monitor polypeptide levels in tissue as part of a clinical testing procedure, e.g., to determine the efficacy of a given treatment regimen.
  • Detection can be facilitated by coupling (i.e., physically linking) the antibody to a detectable substance.
  • detectable substances include various enzymes, prosthetic groups, fluorescent materials, luminescent materials, bioluminescent materials, and radioactive materials.
  • suitable enzymes include horseradish peroxidase, alkaline phosphatase, ⁇ -galactosidase, or acetylcholinesterase;
  • suitable prosthetic group complexes include streptavidin/biotin and avidin/biotin;
  • suitable fluorescent materials include umbelliferone, fluorescein, fluorescein isothiocyanate, rhodamine, dichlorotriazinylamine fluorescein, dansyl chloride or phycoerythrin;
  • an example of a luminescent material includes luminol;
  • bioluminescent materials include luciferase, luciferin, and aequorin, and examples of suitable radioactive material include 125 I,
  • An antibody can be made by immunizing with a purified antigen, or a fragment thereof, a membrane associated antigen, tissues, e.g., crude tissue preparations, whole cells, preferably living cells, lysed cells, or cell fractions.
  • antibodies which bind only a native polypeptide, only denatured or otherwise non-native polypeptide, or which bind both, as well as those having linear or conformational epitopes. Conformational epitopes sometimes can be identified by selecting antibodies that bind to native but not denatured polypeptide. Also featured are antibodies that specifically bind to a polypeptide variant associated with colorectal cancer.
  • the invention includes methods for identifying a candidate therapeutic for treating colorectal cancer.
  • the methods include contacting a test molecule with a target molecule in a system.
  • a target molecule is a nucleic acid molecule having a sequence of any of SEQ ID NOs: 1 to 268, or a fragment thereof, or an encoded polypeptide of SEQ ID NOs:26 ⁇ to 268.
  • the method also includes determining the presence or absence of an interaction between the test molecule and the target molecule, where the presence of an interaction between the test molecule and the nucleic acid or polypeptide identifies the test molecule as a candidate colorectal cancer therapeutic.
  • the interaction between the test molecule and the target molecule may be quantified.
  • Test molecules and candidate therapeutics include compounds, antisense nucleic acids, siRNA molecules, ribozymes, polypeptides or proteins encoded by target nucleic acids, and immunotherapeutics (e.g., antibodies and HLA-presented polypeptide fragments).
  • a test molecule or candidate therapeutic may act as a modulator of target molecule concentration or target molecule function in a system.
  • a modulator may agonize (i.e., up-regulates) or antagonize (i.e., down-regulates) a target molecule concentration partially or completely in a system by affecting such cellular functions as DNA replication and/or DNA processing (e.g., DNA methylation or DNA repair), RNA transcription and/or RNA processing (e.g., removal of intronic sequences and/or translocation of spliced mRNA from the nucleus), polypeptide production (e.g., translation of the polypeptide from mRNA), and/or polypeptide post- translational modification (e.g., glycosylation, phosphorylation, and proteolysis of pro- polypeptides).
  • DNA processing e.g., DNA methylation or DNA repair
  • RNA transcription and/or RNA processing e.g., removal of intronic sequences and/or translocation of spliced mRNA from the nucleus
  • polypeptide production e.g., translation of the poly
  • a modulator may also agonize or antagonize a biological function of a target molecule partially or completely, where the function may include adopting a certain structural conformation, interacting with one or more binding partners, ligand binding, catalysis (e.g., phosphorylation, dephosphorylation, hydrolysis, methylation, and isomerization), and an effect upon a cellular event (e.g., effecting progression of colorectal cancer).
  • catalysis e.g., phosphorylation, dephosphorylation, hydrolysis, methylation, and isomerization
  • an effect upon a cellular event e.g., effecting progression of colorectal cancer
  • a system i.e., a cell free in vitro environment and a cell-based environment such as a collection of cells, a tissue, an organ, or an organism
  • a test molecule in a variety of manners, including adding molecules in solution and allowing them to interact with one another by diffusion, cell injection, and any administration routes in an animal.
  • An interaction refers to an effect of a test molecule on test molecule, where the effect sometimes is binding between the test molecule and the target molecule, and sometimes is an observable change in cells, tissue, or organism.
  • There are known methods for detecting the presence or absence of interaction between a test molecule and a target molecule For example, titrametric, acidimetric, radiometric, NMR, monolayer, polaro graphic, spectrophotometric, fluorescent, and ESR assays probative of a target molecule interaction may be utilized.
  • Test molecule/target molecule interactions can be detected and/or quantified using known assays. For example, an interaction can be determined by labeling the test molecule and/or the target molecule, where the label is covalently or non-covalently attached to the test molecule or target molecule.
  • the label is sometimes a radioactive molecule such as 125 I, S31 1, 35 S or 3 H, which can be detected by direct counting of radio-emission or by scintillation counting.
  • enzymatic labels such as horseradish peroxidase, alkaline phosphatase, or luciferase may be utilized where the enzymatic label can be detected by determining conversion of an appropriate substrate to product.
  • presence or absence of an interaction can be determined without labeling.
  • a microphysiometer e.g., Cytosensor
  • LAPS light-addressable potentiometric sensor
  • cells typically include a nucleic acid from SEQ ID NOs: 1 to 268 or an encoded polypeptide from SEQ ID NOs:261 to 268, and are often of mammalian origin, although the cell can be of any origin.
  • Whole cells, cell homogenates, and cell fractions e.g., cell membrane fractions
  • soluble and/or membrane bound forms of the polypeptide may be utilized.
  • membrane-bound forms of the polypeptide it may be desirable to utilize a solubilizing agent.
  • solubilizing agents include non-ionic detergents such as n-octylglucoside, n-dodecylglucoside, n- dodecylmaltoside, octanoyl-N-methylglucamide, decanoyl-N-methylglucamide, TritonTMX- 10O 5 TritonTM X-114, etc.
  • An interaction between a test molecule and target molecule also can be detected by monitoring fluorescence energy transfer (FET) (see, e.g., Lakowicz et al, U.S. Pat. No, 5,631,169; Stavrianopoulos et al, U.S. Pat. No. 4,868,103).
  • FET fluorescence energy transfer
  • a fluorophore label on a first, donor molecule is selected such that its emitted fluorescent energy will be absorbed by a fluorescent label on a second, acceptor molecule, which in turn is able to fluoresce due to the absorbed energy.
  • the donor polypeptide molecule may simply utilize the natural fluorescent energy of tryptophan residues, Labels are chosen that emit different wavelengths of light, such that the acceptor molecule label may be differentiated from that of the donor. Since the efficiency of energy transfer between the labels is related to the distance separating the molecules, the spatial relationship between the molecules can be assessed. In a situation in which binding occurs between the molecules, the fluorescent emission of the acceptor molecule label in the assay should be maximal.
  • An FET binding event can be conveniently measured through standard fluorometric detection means well known in the art (e.g., using a fluorimeter).
  • determining the presence or absence of an interaction between a test molecule and a target molecule can be effected by monitoring surface plasmon resonance (Sjolander and Urbaniczky, 1991; Szabo et al, 1995).
  • Surface plasmon resonance (SPR) or biomolecular interaction analysis (BIA) can be utilized to detect biospecific interactions in real time, without labeling any of the interactants (e.g., BIAcore).
  • Changes in the mass at the binding surface result in alterations of the refractive index of light near the surface (the optical phenomenon of surface plasmon resonance, resulting in a detectable signal which can be used as an indication of real-time reactions between biological molecules.
  • the target molecule or test molecules are anchored to a solid phase, facilitating the detection of target molecule/test molecule complexes and separation of the complexes from free, uncomplexed molecules.
  • the target molecule or test molecule is immobilized to the solid support.
  • the target molecule is anchored to a solid surface, and the test molecule, which is not anchored, can be labeled, either directly or indirectly, with detectable labels.
  • test molecules may be desirable to immobilize a target molecule, an anti-target molecule antibody, and/or test molecules to facilitate separation of target molecule/test molecule complexes from uncomplexed forms, as well as to accommodate automation of the assay.
  • the attachment between a test molecule and/or target molecule and the solid support may be covalent or non- covalent (see, e.g., U.S. Pat. No. 6,022,688 for non-covalent attachments).
  • the solid support may be one or more surfaces of the system, such as one or more surfaces in each well of a microtiter plate, a surface of a silicon wafer, a surface of a bead (Lam ei a!., 1991) that is optionally linked to another solid support, or a channel in a micro fmidic device, for example.
  • Types of solid supports, linker molecules for covaleiit and non-covalent attachments to solid supports, and methods for immobilizing nucleic acids and other molecules to solid supports are known (see, e.g., U.S. Pat. Nos. 6,261,776; 5,900,481; 6,133,436; and 6,022,688; and WIPO publication WO 01/18234).
  • a target molecule may be immobilized to surfaces via biotin and streptavidin.
  • a biotinylated polypeptide can be prepared from biotin-NHS (N- hydroxysuccinimide, e.g., biotinylation kit, Pierce Chemicals, Rockford, 111.), and immobilized in the wells of streptavidin-coated 96 well plates (Pierce Chemical).
  • a target polypeptide can be prepared as a fusion polypeptide.
  • glutathione-S-transferase/-polypeptide fusion can be adsorbed onto glutathione sepharose beads (Sigma Chemical, St.
  • the beads or microtiter plate wells are washed to remove any unbound components, or the matrix is immobilized in the case of beads, and complex formation is determined directly or indirectly as described above.
  • the complexes can be dissociated from the matrix, and the level of target molecule binding or activity is determined using standard techniques.
  • the non-immobilized component is added to the coated surface containing the anchored component. After the reaction is complete, unreacted components are removed (e.g., by washing) under conditions such that a significant percentage of complexes formed will remain immobilized to the solid surface.
  • the detection of complexes anchored on the solid surface can be accomplished in a number of manners. Where the previously non- immobilized component is pre-labeled, the detection of label immobilized on the surface indicates that complexes were formed.
  • an indirect label can be used to detect complexes anchored on the surface, e.g., by adding a labeled antibody specific for the immobilized component, where the antibody, in turn, can be directly labeled or indirectly labeled with, e.g., a labeled anti-Ig antibody.
  • an assay is performed utilizing antibodies that specifically bind a target molecule or test molecule but do not interfere with binding of the target molecule to the test molecule. Such antibodies can be linked to a solid support, and unbound target molecule may be immobilized by antibody conjugation.
  • Methods for detecting such complexes include immunodetection of complexes using antibodies reactive with the target molecule, as well as enzyme-linked assays which rely on detecting an enzymatic activity associated with the target molecule.
  • Cell free assays also can be conducted in a liquid phase.
  • reaction products are separated from unreacted components, by known techniques, including: differential centrifugation (Rivas and Minton, 1993); electrophoresis (1999) and immunoprecipitation (1999). Media and chromatographic techniques are known (Heegaard, 1998; Hage and Tweed, 1997). Further, fluorescence energy transfer may also be conveniently utilized to detect binding without further purification of the complex from solution.
  • modulators of target molecule expression are identified.
  • a cell or cell free mixture is contacted with a candidate compound and the expression of target mRNA or polypeptide is evaluated relative to the level of expression of target mRNA or polypeptide in the absence of the candidate compound.
  • the candidate compound is identified as an agonist of target mRNA or polypeptide expression.
  • the candidate compound is identified as an antagonist or inhibitor of target mRNA or polypeptide expression.
  • the level of target mRNA or polypeptide expression can be determined by methods described herein.
  • binding partners that interact with a target molecule are detected.
  • the target molecules can interact with one or more cellular or extra-cellular macromolecules, such as polypeptides in vivo, and these interacting molecules or binding partners.
  • Binding partners can agonize or antagonize target molecule biological activity.
  • test molecules that agonize or antagonize interactions between target molecules and binding partners can be useful as therapeutic molecules as they can up-regulate or down-regulated target molecule activity in vivo and thereby treat colorectal cancer.
  • Binding partners of target molecules can be identified by known methods. For example, binding partners may be identified by lysing cells and analyzing cell lysates by electrophoretic techniques. Alternatively, a two-hybrid assay or three-hybrid assay can be utilized (Zervos et al, 1993; Madura ef a/., 1993; Bartel etal., 1993; Iwabuchi etal, 1993): see also, e.g., U.S. Pat. No. 5,283,317 and Brent WO94/10300. A two-hybrid system is based on the modular nature of most transcription factors, which consist of separable DNA-binding and activation domains. The assay often utilizes two different DNA constructs.
  • a nucleic acid from one of SEQ ID NOs:261 to 268, sometimes referred to as the bait is fused to a gene encoding the DNA binding domain of a known transcription factor (e.g., GAL-4).
  • a DNA sequence from a library of DNA sequences that encodes a potential binding partner is fused to a gene that encodes an activation domain of the blown transcription factor.
  • a target nucleic acid can be fused to the activation domain. If the bait and the prey molecules interact in vivo, the DNA-binding and activation domains of the transcription factor are brought into close proximity.
  • reporter gene e.g., lacZ
  • a reporter gene e.g., lacZ
  • Expression of the reporter gene can be detected and cell colonies containing the functional transcription factor can be isolated and used to identify the potential binding partner.
  • a reaction mixture containing the target molecule and the binding partner is prepared, under conditions and for a time sufficient to allow complex formation.
  • the reaction mixture often is provided in the presence or absence of the test molecule.
  • the test molecule can be included initially in the reaction mixture, or can be added at a time subsequent to the addition of the target molecule and its binding partner. Control reaction mixtures are incubated without the test molecule or with a placebo. Formation of any complexes between the target molecule and the binding partner then is detected.
  • Decreased formation of a complex in the reaction mixture containing test molecule as compared to in a control reaction mixture indicates that the molecule antagonizes target molecule/binding partner complex formation.
  • increased formation of a complex in the reaction mixture containing test molecule as compared to in a control reaction mixture indicates that the molecule agonizes target molecule/binding partner complex formation.
  • complex formation of target molecule/binding partner can be compared to complex formation of mutant target molecule/binding partner (e.g., amino acid modifications in a target polypeptide). Such a comparison can be important in those cases where it is desirable to identify test molecules that modulate interactions of mutant but not non-mutated target gene products.
  • the assays can be conducted in a heterogeneous or homogeneous format.
  • a target molecule and/or the binding partner are immobilized to a solid phase, and complexes are detected on the solid phase at the end of the reaction.
  • the entire reaction is carried out in a liquid phase.
  • the order of addition of reactants can be varied to obtain different information about the molecules being tested.
  • test compounds that agonize target molecule/binding partner interactions can be identified by conducting the reaction in the presence of the test molecule in a competition format.
  • test molecules that agonize preformed complexes e.g., molecules with higher binding constants that displace one of the components from the complex, can be tested by adding the test compound to the reaction mixture after complexes have been formed.
  • the target molecule or the binding partner is anchored onto a solid surface (e.g., a microtiter plate), while the non-anchored species is labeled, either directly or indirectly.
  • the anchored molecule can be immobilized by non-covalent or covalent attachments.
  • an immobilized antibody specific for the molecule to be anchored can be used to anchor the molecule to the solid surface.
  • the partner of the immobilized species is exposed to the coated surface with or without the test molecule. After the reaction is complete, unreacted components are removed (e.g., by washing) such that a significant portion of any complexes formed will remain immobilized on the solid surface.
  • the detection of label immobilized on the surface is indicative of complex.
  • an indirect label can be used to detect complexes anchored to the surface; e.g., by using a labeled antibody specific for the initially non-immobilized species.
  • test compounds that inhibit complex formation or that disrupt preformed complexes can be detected.
  • the reaction can be conducted in a liquid phase in the presence or absence of test molecule, where the reaction products are separated from unreacted components, and the complexes are detected (e.g., using an immobilized antibody specific for one of the binding components to anchor any complexes formed in solution, and a labeled antibody specific for the other partner to detect anchored complexes).
  • test compounds that inhibit complex or that disrupt preformed complexes can be identified.
  • a homogeneous assay can be utilized. For example, a preformed complex of the target gene product and the interactive cellular or extra-cellular binding partner-product is prepared. One or both of the target molecule or binding partner is labeled, and the signal generated by the label(s) is quenched upon complex formation (e.g., U.S. Pat. No. 4,109,496 that-utilizes this approach for immunoassays). Addition of a test molecule that competes with and displaces one of the species from the preformed complex will result in the generation of a signal above background. In this way, test substances that disrupt target molecule/binding partner complexes can be identified.
  • Candidate therapeutics for treating colorectal cancer are identified from a group of test molecules that interact with a target molecule.
  • Test molecules are normally ranked according to the degree with which they modulate (e.g., agonize or antagonize) a function associated with the target molecule (e.g., DNA replication and/or processing, RJSfA transcription and/or processing, polypeptide production and/or processing, and/or biological function/activity), and then top ranking modulators are selected.
  • pharmaco genomic information can determine the rank of a modulator.
  • the top 10% of ranked test molecules often are selected for further testing as candidate therapeutics, and sometimes the top 15%, 20%, or 25% of ranked test molecules are selected for further testing as candidate therapeutics.
  • Candidate therapeutics typically are formulated for administration to a subject.
  • Formulations, medicaments and pharmaceutical compositions typically include in combination with a pharmaceutically acceptable carrier one or more target molecule modulators.
  • the modulator often is a test molecule identified as having an interaction with a target molecule by a screening method.
  • the modulator may be a compound, an antisense nucleic acid, a ribozyme, an antibody, or a binding partner.
  • formulations may include a polypeptide combination with a pharmaceutically acceptable carrier.
  • a pharmaceutically acceptable carrier includes solvents, dispersion media, coatings, antibacterial and antifungal agents, isotonic and absorption delaying agents, and the like, compatible with pharmaceutical administration. See for example, Remington's Pharmaceutical Sciences (2005). Supplementary active compounds can also be incorporated into the compositions. Pharmaceutical compositions can be included in a container, pack, or dispenser together with instructions for administration.
  • a pharmaceutical composition typically is formulated to be compatible with its intended route of administration.
  • routes of administration include parenteral, e.g., intravenous, intradermal, subcutaneous, oral (e.g., inhalation), transdermal (topical), transmucosal, and rectal administrations
  • Solutions or suspensions used for parenteral, intradermal, or subcutaneous application can include the following components: a sterile diluent such as water for injection, saline solution, fixed oils, polyethylene glycols, glycerin, propylene glycol or other synthetic solvents; antibacterial agents such as benzyl alcohol or methyl parabens; antioxidants such as ascorbic acid or sodium bisulfite; chelating agents such as ethylenediamlnetetraacetlc acid; buffers such as acetates, citrates or phosphates and agents for the adjustment of tonicity such as sodium chloride or dextrose. pH can be adjusted with acids or bases, such as hydrochloric
  • Oral compositions generally include an inert diluent or an edible carrier.
  • the active compound can be incorporated with excipients and used in the fo ⁇ ii of tablets, troches, or capsules, e.g., gelatin capsules.
  • Oral compositions can also be prepared using a fluid carrier for use as a mouthwash.
  • Pharmaceutically compatible binding agents, and/or adjuvant materials can be included as part of the composition.
  • the tablets, pills, capsules, troches and the like can contain any of the following ingredients, or compounds of a similar nature: a binder such as micro crystalline cellulose, gum tragacanth or gelatin; an excipient such as starch or lactose, a disintegrating agent such as alginic acid, Primogel, or corn starch; a lubricant such as magnesium stearate; a glidant such as colloidal silicon dioxide; a sweetening agent such as sucrose or saccharin; or a flavoring agent such as peppermint, methyl salicylate, or orange flavoring.
  • a binder such as micro crystalline cellulose, gum tragacanth or gelatin
  • an excipient such as starch or lactose, a disintegrating agent such as alginic acid, Primogel, or corn starch
  • a lubricant such as magnesium stearate
  • a glidant such as colloidal silicon dioxide
  • a sweetening agent such as sucrose or
  • compositions suitable for injectable use include sterile aqueous solutions (where water soluble) or dispersions and sterile powders for the extemporaneous preparation of sterile injectable solutions or dispersion.
  • suitable carriers include physiological saline, bacteriostatic water, Cremophor ELTM (BASF, Parsippany, NJ.) or phosphate buffered saline (PBS).
  • the composition must be sterile and should be fluid to the extent that easy syringability exists. It should be stable under the conditions of manufacture and storage and must be preserved against the contaminating action of microorganisms such as bacteria and fungi.
  • the carrier can be a solvent or dispersion medium containing, for example, water, ethanol, polyol (for example, glycerol, propylene glycol, and liquid polyethylene glycol, and the like), and suitable mixtures thereof.
  • the proper fluidity can be maintained, for example, by the use of a coating such as lecithin, by the maintenance of the required particle size in the case of dispersion and by the use of surfactants.
  • Prevention of the action of microorganisms can be achieved by various antibacterial and antifungal agents, for example, parabens, chlorobutanol, phenol, ascorbic acid, thimerosal, and the like.
  • isotonic agents for example, sugars, polyalcohols such as mannitol or sorbitol, and/or sodium chloride in the composition.
  • Prolonged absorption of the injectable compositions can be brought about by including in the composition an agent which delays absorption, for example, aluminum monostearate and gelatin.
  • Sterile injectable solutions can be prepared by incorporating the active compound in the required amount in an appropriate solvent with one or a combination of ingredients enumerated above, as required, followed by filtered sterilization.
  • dispersions are prepared by incorporating the active compound into a sterile vehicle which contains a basic dispersion medium, and the required other ingredients from those enumerated above.
  • the methods of preparation often utilized are vacuum drying and freeze-drying which yields a powder of the active ingredient plus any additional desired ingredient from a previously sterile-filtered solution thereof.
  • Systemic administration might be by transmucosal or transdermal means.
  • penetrants appropriate to the barrier to be permeated are used in the formulation.
  • penetrants are generally known in the art, and include, for example, for transmucosal administration, detergents, bile salts, and fusidic acid derivatives.
  • Transmucosal administration can be accomplished through the use of nasal sprays or suppositories.
  • the active compounds are formulated into ointments, salves, gels, or creams as generally known in the art.
  • Molecules can also be prepared in the form of suppositories (e.g., with conventional suppository bases such as cocoa butter and other glycerides) or retention enemas for rectal delivery.
  • active molecules are prepared with carriers that will protect the compound against rapid elimination from the body, such as a controlled release formulation, including implants and microencapsulated delivery systems.
  • a controlled release formulation including implants and microencapsulated delivery systems.
  • Biodegradable, biocompatible polymers can be used, such as ethylene vinyl acetate, polyanhydrides, polyglycolic acid, collagen, polyorthoesters, and polylactic acid. Methods for preparation of such formulations will be apparent to those skilled in the art. Materials can also be obtained commercially from Alza Corporation and Nova Pharmaceuticals, Inc. Liposomal suspensions (including liposomes targeted to infected cells with monoclonal antibodies to viral antigens) can also be used as pharmaceutically acceptable carriers. These can be prepared according to methods known to those skilled in the art, for example, as described in U.S. Pat. No. 4,522,811.
  • compositions in dosage unit form for ease of administration and uniformity of dosage.
  • Each unit containing a predetermined quantity of active compound is calculated to produce the desired therapeutic effect in association with the required pharmaceutical carrier.
  • Toxicity and therapeutic efficacy of such compounds can be determined by standard pharmaceutical procedures in cell cultures or experimental animals, e.g., for determining the LD 50 (the dose lethal to 50% of the population) and the ED.sub.50 (the dose therapeutically effective in 50% of the population).
  • the dose ratio between toxic and therapeutic effects is the therapeutic index and it can be expressed as the ratio LD 50 /ED 50 .
  • Molecules which exhibit high therapeutic indices often are utilized. While molecules that exhibit toxic side effects may be used, care should be taken to design a delivery system that targets such compounds to the site of affected tissue in order to minimize potential damage to uninfected cells and, thereby, reduce side effects.
  • the data obtained from the cell culture assays and animal studies can be used in formulating a range of dosage for use in humans.
  • the dosage of such molecules typically lies within a range of circulating concentrations that include the ED 50 with little or no toxicity.
  • the dosage may vary within this range depending upon the dosage form employed and the route of administration utilized.
  • the therapeutically effective dose can be estimated initially from cell culture assays.
  • a dose may be formulated in animal models to achieve a circulating plasma concentration range that includes the IC. sub.50 (i.e., the concentration of the test compound which achieves a half- maximal inhibition of symptoms) as determined in cell culture.
  • IC. sub.50 i.e., the concentration of the test compound which achieves a half- maximal inhibition of symptoms
  • levels in plasma may be measured, for example, by high performance liquid chromatography.
  • a therapeutically effective amount of protein or polypeptide ranges from about 0.001 to 30 mg/kg body weight, sometimes about 0.01 to 25 mg/kg body weight, often about 0.1 to 20 mg/kg body weight, and more often about 1 to 10 mg/kg, 2 to 9 mg/kg, 3 to 8 mg/kg, 4 to 7 mg/kg, or 5 to 6 mg/kg body weight.
  • the protein or polypeptide can be administered one time per week for between about 1 to 10 weeks, sometimes between 2 to 8 weeks, often between about 3 to 7 weeks, and more often for about 4, 5, or 6 weeks.
  • treatment of a subject with a therapeutically effective amount of a protein, polypeptide, or antibody can include a single treatment or, can include a series of treatments.
  • a dosage of 0.1 mg/kg of body weight (generally 10 mg/kg to 20 mg/kg) is often utilized. If the antibody is to act in the brain, a dosage of 50 mg/kg to 100 mg/kg is often appropriate. Generally, partially human antibodies and fully human antibodies have a longer half-life within the human body than other antibodies. Accordingly, lower dosage and less frequent administration is often possible. Modifications such as lipidation can be used to stabilize antibodies and to enhance uptake and tissue penetration (e.g., into the brain). A method for lipidation of antibodies is described by Cruikshank et al (Cruikshank et al., 1997).
  • Antibody conjugates can be used for modifying a given biological response, the drug moiety is not to be construed as limited to classical chemical therapeutic agents.
  • the drug moiety may be a protein or polypeptide possessing a desired biological activity.
  • proteins may include, for example, a toxin such as abrin, ricin A, pseudomonas exotoxin, or diphtheria toxin; a polypeptide such as tumor necrosis factor, alpha-interferon, beta- interferon, nerve growth factor, platelet derived growth factor, tissue plasminogen activator; or, biological response modifiers such as, for example, lymphokines, interleukin-1 ("IL-I”), interleukin-2 (“IL-2”), interleukin-6 (“IL-6”), granulocyte macrophage colony stimulating factor (“GM-CSF”), granulocyte colony stimulating factor (“G-CSF”), or other growth factors.
  • an antibody can be conjugated to a second antibody to form an antibody heteroconjugate
  • exemplary doses include milligram or microgram amounts of the compound per kilogram of subject or sample weight, for example, about 1 microgram per kilogram to about 500 milligrams per kilogram, about 100 micrograms per kilogram to about 5 milligrams per kilogram, or about 1 microgram per kilogram to about 50 micrograms per kilogram. It is understood that appropriate doses of a small molecule depend upon the potency of the small molecule with respect to the expression or activity to be modulated.
  • a physician, veterinarian, or researcher may, for example, prescribe a relatively low dose at first, subsequently increasing the dose until an appropriate response is obtained.
  • the specific dose level for any particular animal subject will depend upon a variety of factors including the activity of the specific compound employed, the age, body weight, general health, gender, and diet of the subject, the time of administration, the route of administration, the rate of excretion, any drug combination, and the degree of expression or activity to be modulated.
  • gene therapy vectors can be delivered to a subject by, for example, intravenous injection, local administration (see, e.g., U.S. Pat. No.
  • compositions of gene therapy vectors can include a gene therapy vector in an acceptable diluent, or can comprise a slow release matrix in which the gene delivery vehicle is imbedded.
  • the pharmaceutical preparation can include one or more cells which produce the gene delivery system. Examples of gene delivery vectors are described herein.
  • a therapeutic formulation described above can be administered to a subject in need of a therapeutic for treating colorectal cancer.
  • Therapeutic formulations can be administered by any of the paths described herein. With regard to both prophylactic and therapeutic methods of treatment, such treatments may be specifically tailored or modified, based on knowledge obtained from pharmacogenomic analyses described herein.
  • a treatment is the application or administration of a therapeutic formulation to a subject, or application or administration of a therapeutic agent to an isolated tissue or cell line from a subject with the purpose to cure, heal, alleviate, relieve, alter, remedy, ameliorate, improve or affect colorectal cancer, symptoms of colorectal cancer or a predisposition towards colorectal cancer.
  • a therapeutic formulation includes small molecules, peptides, antibodies, ribozymes and antisense oligonucleotides. Administration of a therapeutic formulation can occur prior to the manifestation of symptoms characteristic of colorectal cancer, such that the cancer is prevented or delayed in its progression.
  • the appropriate therapeutic composition can be determined based on screening assays described herein.
  • modulators include, but are not limited to, small organic or inorganic molecules; antibodies (including, for example, polyclonal, monoclonal, humanized, anti-idiotypic, chimeric or single chain antibodies, and FAb, F(ab') 2 and FAb expression library fragments, scFV molecules, and epitope-binding fragments thereof); and peptides, phosphopeptides, or polypeptides.
  • antisense and ribozyme molecules that inhibit expression of the target gene can also be used to reduce the level of target gene expression, thus effectively reducing the level of target gene activity.
  • triple helix molecules can be utilized in reducing the level of target gene activity.
  • Antisense, ribozyme and triple helix molecules are discussed above. It is possible that the use of antisense, ribozyme, and/or triple helix molecules to reduce or inhibit mutant gene expression can also reduce or inhibit the transcription (triple helix) and/or translation (antisense, ribozyme) of mRNA produced by normal target gene alleles, such that the concentration of normal target gene product present can be lower than is necessary for a normal phenotype.
  • nucleic acid molecules that encode and express target gene polypeptides exhibiting normal target gene activity can be introduced into cells via gene therapy method.
  • the target gene encodes an extra-cellular polypeptide
  • it can be preferable to co-administer normal target gene polypeptide into the cell or tissue in order to maintain the requisite level of cellular or tissue target gene activity.
  • nucleic acid molecules may be utilized in treating or preventing colorectal cancer.
  • Aptamers are nucleic acid molecules having a tertiary structure which permits them to specifically bind to ligands (Osborne et al., 1997; PateL 1997).
  • the invention thus includes a gene therapy method for treating colorectal cancer in a subject, which includes contacting one or more cells in the subject or from the subject with a nucleic acid having a first nucleotide sequence.
  • Genomic DNA in the subject includes a second nucleotide sequence having one or more SNPs associated with colorectal cancer.
  • the first and second nucleotide sequences typically are substantially identical to one another, and the first nucleotide sequence comprises fewer SNPs associated with colorectal cancer than the second nucleotide sequence.
  • the first nucleotide sequence may comprise a gene sequence that encodes a full-length polypeptide or a fragment thereof.
  • the subject is often a human. Allele therapy methods often are utilized in conjunction with a method of first determining whether a subject has genomic DNA that includes SNPs associated with colorectal cancer.
  • Another allele therapy is a method which comprises contacting one or more cells in the subject or from the subject with a polypeptide encoded by a nucleic acid having a first nucleotide sequence.
  • Genomic DNA in the subject includes a second nucleotide sequence having one or more SNPs associated with colorectal cancer.
  • the first and second nucleotide sequences typically are substantially identical to one another, and the first nucleotide sequence includes fewer SNPs associated with colorectal cancer than the second nucleotide sequence.
  • the first nucleotide sequence may include a gene sequence that encodes a full- length polypeptide or a fragment thereof.
  • the subject is usually a human.
  • antibodies can be generated that are both specific for target molecules and that reduce target molecule activity. Such antibodies may be administered in instances where antagonizing a target molecule function is appropriate for the treatment of colorectal cancer.
  • Lipofectin or liposomes can be used to deliver the antibody or a fragment of the Fab region that binds to the target antigen into cells. Where fragments of the antibody are used, the smallest inhibitory fragment that binds to the target antigen often is utilized. For example, peptides having an amino acid sequence corresponding to the Fv region of the antibody can be used.
  • single chain neutralizing antibodies that bind to intracellular target antigens can also be administered. Such single chain antibodies can be administered, for example, by expressing nucleotide sequences encoding single-chain antibodies within the target cell population (Marasco et al, 1993).
  • Modulators can be administered to a patient at therapeutically effective doses to treat colorectal cancer.
  • a therapeutically effective dose refers to an amount of the modulator sufficient to result in amelioration of symptoms of colorectal cancer.
  • Toxicity and therapeutic efficacy of modulators can be determined by standard pharmaceutical procedures in cell cultures or experimental animals, e.g., for determining the LD 50 (the dose lethal to 50% of the population) and the ED 50 (the dose therapeutically effective in 50% of the population).
  • the dose ratio between toxic and therapeutic effects is the therapeutic index and it can be expressed as the ratio LD 50 /ED 50 .
  • Modulators that exhibit large therapeutic indices often are utilized. While modulators that exhibit toxic side effects can be used, care should be taken to design a delivery system that targets such molecules to the site of affected tissue in order to minimize potential damage to uninfected cells, thereby reducing side effects.
  • Data obtained from cell culture assays and animal studies can be used in formulating a range of dosages for use in humans.
  • the dosage of such compounds typically lies within a range of circulating concentrations that include the ED 50 with little or no toxicity.
  • the dosage can vary within this range depending upon the dosage form employed and the route of administration utilized.
  • the therapeutically effective dose can be estimated initially from cell culture assays.
  • a dose can be formulated in animal models to achieve a circulating plasma concentration range that includes the IC 50 (i.e., the concentration of the test compound that achieves a half- maximal inhibition of symptoms) as determined in cell culture.
  • IC 50 i.e., the concentration of the test compound that achieves a half- maximal inhibition of symptoms
  • levels in plasma can be measured, for example, by high performance liquid chromatography.
  • Another example of effective dose determination for an individual is the ability to directly assay levels of "free" and "bound” compound in the serum of the test subject.
  • Such assays may utilize antibody mimics and/or "biosensors” that have been created through molecular imprinting techniques.
  • Molecules that modulate target molecule activity are used as a template, or "imprinting molecule”, to spatially organize polymerizable monomers prior to their polymerization with catalytic reagents. The subsequent removal of the imprinted molecule leaves a polymer matrix which contains a repeated "negative image” of the compound and is able to selectively rebind the molecule under biological assay conditions.
  • Such "imprinted" affinity matrixes are amenable to ligand-binding assays, whereby the immobilized monoclonal antibody component is replaced by an appropriately imprinted matrix.
  • An example of the use of such matrixes in this way can be seen in Vlatakis, et al, (Vlatakis et al, 1993).
  • isotope-labeling Through the use of isotope-labeling, the "free" concentration of compound which modulates target molecule expression or activity readily can be monitored and used in calculations of IC 50 .
  • Such "imprinted” affinity matrixes can also be designed to include fluorescent groups whose photon-emitting properties measurably change upon local and selective binding of target compound. These changes readily can be assayed in real time using appropriate fiberoptic devices, in turn allowing the dose in a test subject to be quickly optimized based on its individual IC50.
  • Genomic DNA samples from patients aged 25-74 and patients with both familial and sporadic CRC with family and unrelated ethnically matched controls were studied.
  • We identified CRC-associated alleles by measuring 99,632 single nucleotide polymorphisms in peripheral blood DNA from 2,475 subjects (1,234 cases with colorectal cancer and 1,241 age matched individuals undiseased at the time of testing), and validating the identified CRC-associated alleles by using peripheral blood DNA from a second, different, group of 2,194 subjects
  • the SNPs were analyzed on DNA from our control and study population using either the Illumina Bead Array system (http://www.illumina.com; Illumina, Inc., 9885 Towne Centre Drive, San Diego, CA 92121-1975), the MIP platform (http://www.affymetrix.com, Affymetrix, Inc., 3380 Central Expressway, Santa Clara, CA 95051), the Affymetrix GeneChip® Human Mapping IOOK Set platform (http://www.affymetrix.com, Affymetrix, Inc., 3380 Central Expressway, Santa Clara, CA 95051), or the Affymetrix GeneChip® Human Mapping 500K Array Set platform (http://www.affymetrix.com, Affymetrix, Inc., 3380 Central Expressway, Santa Clara, CA 95051).
  • the SNPs for the IUumina Bead Array system were selected on the basis of being associated with genes involved in DNA repair, chromosomal stability or signal transduction and expressed in human colon epithelium.
  • the SNPs for the MIP platform were selected to include most SNPs that would alter the coding sequence of a protein product.
  • the SNPs for the Affymetrix GeneChip® Human Mapping IOOK Set platform were selected as to cover the entire genome, but the SNPs were preferentially selected in genie regions present on Xba ⁇ or Hin ⁇ lll restriction fragments varying in length from about 250 base pairs to about 2000 base pairs.
  • the SNPs for the Affymetrix GeneChip® Human Mapping 500K Array Set platforms were selected as to cover the entire genome, but the SNPs were preferentially selected in genie regions present on Nspl and Styl restriction fragments varying in length from about 200 base pairs to about 1100 base pairs. Data was stored and organized using the Nanuq informatics environment of the McGiIl University and Genome Quebec Innovation Centre (http://www.genomequebec.mcgill.ca/; McGiIl University and Genome Quebec Innovation Centre, 740, Dondel Penfield Avenue, Montreal, Quebec H3A 1 A4). Allele frequencies found within DNA from patients with colorectal cancer and those without this disease were compared using the univariate Mantel-Haenszel Chi-Square statistic.
  • the inventors of the present invention have discovered single base pair polymorphisms that are present in a highly significant percentage of the genetic DNA of individuals affected with colorectal cancer while only present in a smaller percentage of individuals who are not known to be affected by the disease.
  • Table IA indicates SNPs found to be in strong linkage disequilibrium with rs6533603. To generate this list, correlation coefficients (r 2 ) were calculated between the index SNP and all neighboring SNPs cited in the January 2007 HapMap data set release. An r 2 cut off of 0.50 was selected for inclusion as evidence for strong genetic linkage, i.e., a "strong linkage disequilibrium".
  • Table 2A indicates SNPs found to be in strong linkage disequilibrium with rs2517448. To generate this list, correlation coefficients (r 2 ) were calculated between the index SNP and all neighboring SNPs cited in the January 2007 HapMap data set release. An r 1 cut off of 0.50 was selected for inclusion as evidence for strong genetic linkage, i.e., a "strong linkage disequilibrium".
  • Table 3A indicates SNPs found to be in strong linkage disequilibrium with rs6457327. To generate this list, correlation coefficients (r 2 ) were calculated between the index SNP and all neighboring SNPs cited in the January 2007 HapMap data set release. An r 2 cut off of 0.50 was selected for inclusion as evidence for strong genetic linkage, i.e., a "strong linkage disequilibrium".
  • Table 4A indicates SNPs found to be in strong linkage disequilibrium with rs3130573. To generate this list, con-elation coefficients (r 2 ) were calculated between the index SNP and all neighboring SNPs cited in the January 2007 HapMap data set release. An r 2 cut off of 0.50 was selected for inclusion as evidence for strong genetic linkage, i.e., a "strong linkage disequilibrium".
  • Table 5A indicates SNPs found to be in strong linkage disequilibrium with rsl265086. To generate this list, correlation coefficients (r 2 ) were calculated between the index SNP and all neighboring SNPs cited in the January 2007 HapMap data set release. An r 2 cut off of 0.50 was selected for inclusion as evidence for strong genetic linkage, i.e., a "strong linkage disequilibrium".
  • Table 6A indicates SNPs found to be in strong linkage disequilibrium with rsl2651 12. To generate this list, correlation coefficients (r 2 ) were calculated between the index SNP and all neighboring SNPs cited in the January 2007 HapMap data set release. An r 2 cut off of 0.50 was selected for inclusion as evidence for strong genetic linkage, i.e., a "strong linkage disequilibrium".
  • Table 7A indicates SNPs found to be in strong linkage disequilibrium with rs720465. To generate this list, correlation coefficients (r 2 ) were calculated between the index SNP and all neighboring SNPs cited in the January 2007 HapMap data set release. An r 2 cut off of 0.50 was selected for inclusion as evidence for strong genetic linkage, i.e., a "strong linkage disequilibrium".
  • Table 8A indicates SNPs found to be in strong linkage disequilibrium with rsl265159. To generate this list, correlation coefficients (r 2 ) were calculated between the index SNP and all neighboring SNPs cited in the January 2007 HapMap data set release, An r 2 cut off of 0.50 was selected for inclusion as evidence for strong genetic linkage, i.e., a "strong linkage disequilibrium".
  • Table 9A indicates SNPs found to be in strong linkage disequilibrium with rs3130467. To generate this list, correlation coefficients (r 2 ) were calculated between the index SNP and all neighboring SNPs cited in the January 2007 HapMap data set release. An r 2 cut off of 0.50 was selected for inclusion as evidence for strong genetic linkage, i.e., a "strong linkage disequilibrium".
  • Table 1OA indicates SNPs found to be in strong linkage disequilibrium with rs3130473. To generate this list, correlation coefficients (r 2 ) were calculated between the index SNP and all neighboring SNPs cited in the January 2007 HapMap data set release. An r 2 cut off of 0.50 was selected for inclusion as evidence for strong genetic linkage, i.e., a "strong linkage disequilibrium".
  • Table HA indicates SNPs found to be in strong linkage disequilibrium with rs7014346. To generate this list, correlation coefficients (r 2 ) were calculated between the index SNP and all neighboring SNPs cited in the January 2007 HapMap data set release. An r 2 cut off of 0.50 was selected for inclusion as evidence for strong genetic linkage, i.e., a "strong linkage disequilibrium".
  • Table 12A indicates SNPs found to be in strong linkage disequilibrium with rs7842552. To generate this list, correlation coefficients (r 2 ) were calculated between the index SNP and all neighboring SNPs cited in the January 2007 HapMap data set release. An r 2 cut off of 0.50 was selected for inclusion as evidence for strong genetic linkage, i.e., a "strong linkage disequilibrium".
  • Table 13A indicates SNPs found to be hi strong linkage disequilibrium with rsl 1213809. To generate this list, correlation coefficients (r 2 ) were calculated between the index SNP and all neighboring SNPs cited in the January 2007 HapMap data set release. An r 2 cut off of 0.50 was selected for inclusion as evidence for strong genetic linkage, i.e., a "strong linkage disequilibrium".
  • Table 14A indicates SNPs found to be in strong linkage disequilibrium with rs3802S42. To generate this list, correlation coefficients (r 2 ) were calculated between the index SNP and all neighboring SNPs cited in the January 2007 HapMap data set release. An r 2 cut off of 0.50 was selected for inclusion as evidence for strong genetic linkage, i.e., a "strong linkage disequilibrium".
  • Table 15A indicates SNPs found to be in strong linkage disequilibrium with rs7947952. To generate this list, correlation coefficients (r 2 ) were calculated between the index SNP and all neighboring SNPs cited in the January 2007 HapMap data set release. An r 2 cut off of 0.50 was selected for inclusion as evidence for strong genetic linkage, i.e., a "strong linkage disequilibrium".
  • Table 16A indicates SNPs found to be in strong linkage disequilibrium with rsl 0749971. To generate this list, correlation coefficients (r 2 ) were calculated between the index SNP and all neighboring SNPs cited in the January 2007 HapMap data set release. An r 2 cut off of 0.50 was selected for inclusion as
  • Table 17A indicates SNPs found to be in strong linkage disequilibrium with rs4514461. To generate this list, correlation coefficients (r 2 ) were calculated between the index SNP and all neighboring SNPs cited in the January 2007 HapMap data set release. An r 2 cut off of 0.50 was selected for inclusion as evidence for strong genetic linkage, i.e., a "strong linkage disequilibrium".
  • Table 18A indicates SNPs found to be in strong linkage disequilibrium with rsl2799202. To generate this list, correlation coefficients (r 2 ) were calculated between the index SNP and all neighboring SNPs cited in the January 2007 HapMap data set release. An r 2 cut off of 0.50 was selected for inclusion as evidence for strong genetic linkage, i.e., a "strong linkage disequilibrium".
  • Table 19A indicates SNPs found to be in strong linkage disequilibrium with rs4939827. To generate this list, correlation coefficients (r 2 ) were calculated between the index SNP and all neighboring SNPs cited in the January 2007 HapMap data set release. An r 2 cut off of 0.50 was selected for inclusion as evidence for strong genetic linkage, i.e., a "strong linkage disequilibrium".
  • Table 2OA indicates SNPs found to be in strong linkage disequilibrium with rsl2953717. To generate this list, correlation coefficients (r 2 ) were calculated between the index SNP and all neighboring SNPs cited in the January 2007 HapMap data set release. An r 2 cut off of 0.50 was selected for inclusion as evidence for strong genetic linkage, i.e., a "strong linkage disequilibrium".
  • Table 21A indicates SNPs found to be in strong linkage disequilibrium with rs9951602. To generate this list, con-elation coefficients (r 2 ) were calculated between the index SNP and all neighboring SNPs cited in the January 2007 HapMap data set release. An r 2 cut off of 0.50 was selected for inclusion as evidence for strong genetic linkage, i.e., a "strong linkage disequilibrium".
  • Another aspect of the invention is a method of diagnosing colorectal cancer in an individual, or determining whether the individual is at altered risk for colorectal cancer, by detecting polymorphism in a subject by treating a tissue sample from the subject with an antibody to a polymorphic genetic variant of the present invention and detecting binding of said antibody.
  • a person of skill in the art would know how to produce such an antibody (see, for instance, Harlow, E.
  • Such antibodies may include, but are not limited to polyclonal antibodies, monoclonal antibodies (mAbs), humanized or chimeric antibodies, single chain antibodies, Fab fragments, F(ab') 2 fragments, fragments produced by a Fab expression library, aiiti -idiotypic (anti-Id) antibodies, and epitope-binding fragments of any of the above.
  • mAbs monoclonal antibodies
  • Fab fragments fragments
  • F(ab') 2 fragments fragments produced by a Fab expression library
  • aiiti -idiotypic (anti-Id) antibodies fragments produced by a Fab expression library
  • anti-Id aiiti -idiotypic antibodies
  • transgenic mice which contain a specific allelic variant of a containing any of the SNPs disclosed herein. These mice can be created, e.g., by replacing their wild-type gene with an allele containing a SNP disclosed herein, or of the corresponding human gene containing such a SNP.
  • the present invention provides a transgenic mammalian animal, said animal having cells incorporating a recombinant expression system adapted to express a gene containing a SNP disclosed herein (preferably the human gene containing a SNP disclosed herein).
  • a recombinant expression system will be stably integrated into the genome of the transgenic animal and will thus be heritable so that the offspring of such a transgenic animal may themselves contain the transgene.
  • Transgenic animals can be engineered by introducing the a nucleic acid molecule containing only the coding portion of the gene into the genome of animals of interest, using standard techniques for producing transgenic animals.
  • Animals that can serve as a target for transgenic manipulation include, without limitation, mice, rats, rabbits, guinea pigs, sheep, goats, pigs, and non-human primates, e.g. baboons, chimpanzees and monkeys.
  • Techniques known in the art to introduce a transgene into such animals include pronucleic microinjection (U.S. Pat. No. 4,873,191); retrovirus-mediated gene transfer into germ lines (e.g. Van der Putten et at. 1985, Proc. Natl. Acad. Sci.
  • transgenic animals include those that carry the recombinant molecule only in part of their cells ("mosaic animals").
  • the molecule can be integrated either as a single transgene, or in concatamers. Selective introduction of a nucleic acid molecule into a particular cell type is also possible by following, for example, the technique of Lasko et al. , Proc. Natl, Acad. Sci.
  • GWA Genome-wide association
  • Phase 1 The London Phase 1 was based on genotyping 940 cases with familial colorectal neoplasia and 965 controls ascertained through the CORGI consortium for 555,352 SNPs using the Illumina HumanHap550 BeadChip Array. Phase 1 in the Edinburgh study consisted of genotyping 1,012 early-onset (aged ⁇ 55 years) Scottish CRC cases and 1,012 controls for 555,510 SNPs using the Illumina HumanHap300 and HumanHap240S arrays.
  • Phase 2 was based on genotyping 42,708 SNPs in total. After applying quality control filters the following data were available: London Phase 2 38,715 polymorphic SNPs in 2,854 cases and 2,822 controls; and Edinburgh Phase 2 38,710 polymorphic SNPs in 2,024 cases and 2,092 controls. Overall, there were 38,710 polymorphic SNPs common to all four data sets (Phases 1 and 2 in London and Edinburgh).
  • expression quantitative trait locus analyses may aid elucidation of causality. While examination of genotypic effects on expression in lymphoblastoid cell lines can be informative if genes are ubiquitously expressed, it is likely to be limited by tissue-specific effects. Furthermore, the target tissue need not even be the organ or cell type from which cancer develops.
  • Table 23 (see below) provides a summary of all cases and controls in the study.
  • 1,012 CRC cases (518 males, 494 females; mean age at diagnosis 49.6 years; SD ⁇ 6.1) and 1,012 age- and gender- matched cancer-free population controls (518 males, 494 females; mean age 51.0 years; SD ⁇ 5.9). Cases were enriched for genetic aetiology by early age at onset (age ⁇ 55 years). Known dominant polyposis syndromes, HNPCC or bi-allelic MYH mutation carriers were excluded. Control subjects were population controls, matched by age ( ⁇ 5 years), gender and area of residence within Scotland.
  • Phase 2 2,057 CRC cases (1,249 males, 808 females; mean age at diagnosis 65.8 years; SD ⁇ 8.4) and 2,111 population controls (1,257 males, 854 females; mean age 67.9 years; SD ⁇ 9.0) ascertained in Scotland. Cases were taken from an independent, prospective, incident colorectal cancer case series and aged ⁇ 80 years at diagnosis. Control subjects were population controls matched by age ( ⁇ 5 years), gender and area of residence within Scotland.
  • VCQ58 1543 CRC cases (925 males, 618 females, mean age of diagnosis 62.4 years; SD ⁇ 10.7), consisting of 1234 (2 SNPS typed for 1310) samples from the VICTOR/QUASAR2 trials and 309 CRC cases collected through the CORGI study.
  • FCCPS 962 CRC cases (509 males, 452 females, 1 unknown; mean age at diagnosis 66.9 years; SD ⁇ 12.2) and 846 controls (randomly selected anonymous Finnish blood donors) ascertained in south-eastern Finland.
  • DACHS 1,373 CRC cases (790 males, 583 females; mean age at diagnosis 68.1 years; SD ⁇ 10.4) and 1,480 controls (719 males, 761 females; mean age 68.0 years; SD ⁇ 9.9) ascertained through the Darmkrebs: Chancen der Verhutung Anlagen (DACHS) 5 a population based case-control study of incident CRC in the Rhine-Neckar-Odenwald region around Heidelberg between 2003 and 2006.
  • Kiel 2,169 CRC cases (1,089 males, 1,080 females; mean age at diagnosis 60.9 years; SD ⁇ 8.8) and 2,145 controls (1,059 males, 1,086 females; mean age 64.7 years; SD ⁇ 10.0) ascertained through the POPGEN and SHIP population-based biobank projects based in Kiel and Greifswald, Germany. 5
  • CRC was defined according to the ninth revision of the International Classification of Diseases (ICD) by codes 153-154 32 and all cases had pathologically proven adenocarcinoma or adenomas.
  • ICD International Classification of Diseases
  • the London Phase 1 GWAS was conducted using the Illumina HumanHap550 Bead Arrays and the Edinburgh Phase 1 GWAS was conducted using the Illumina HumanHap300 and HumanHap240S according to the manufacturer's protocols. DNA samples with GenCall scores ⁇ 0.25 at any locus were considered "no calls”. In London and Edinburgh Phase 2 genotyping was conducted using Illumina Minium custom arrays
  • Micro satellite instability (MSI) in CRCs was determined using the following methodology; lOum sections were cut from formalin fixed paraffin embedded tumours, lightly stained with toluidine blue, and regions containing at least 60% tumour micro-dissected. Tumour DNA was extracted using the QIAamp DNA Mini kit (Qiagen, Crawley, UK) according to the manufacturer's instructions and geno typed for the mononucleotide microsatellite loci BAT25 and BAT26 which are highly sensitive markers of MSI 33 . Samples showing novel alleles at either BAT26 or BAT25 or both markers were assigned as MSI (corresponding to a high level of instability, MSI-H 34 ).
  • Genotype data were used to search for duplicates and closely related individuals amongst all samples in Phases 1 and 2. Identity by state values were calculated for each pair of individuals, and for any pair with allele sharing > 80%, the sample generating the lowest call rate was removed from further analysis.
  • genotyped samples were excluded from analyses for the following reasons: carriers of another susceptibility allele (5 cases), first-degree relative with CRC (11 controls); duplicated (2 cases, 7 controls); relatedness (1 case, 15 controls).
  • genotyped samples were excluded from analyses for the following reasons: duplicated (8 cases, 2 controls); relatedness (2 cases, 18 controls); gender discrepancies (13 controls).
  • Edinburgh Phases 1 and 2 genotyped samples were excluded from analyses for the following reasons: identified as of non-Caucasian descent (7 in Phase 1, 3 in Phase 2); previously unrecognised carriers of another susceptibility allele (5 DNA mismatch repair gene mutation carriers in Phase 2); gender discrepancies between records and genotype (14 in Phase 1, 22 in Phase 2); hidden relatedness (5 in Phase 1).
  • the adequacy of the case-control matching and possibility of differential genotyping of cases and controls was formally evaluated using Q-Q plots of test statistics.
  • the inflation factor D was calculated by dividing the mean of the lower 90% of the test statistics by the mean of the lower 90% of the expected values from a D 2 distribution with 1 d.f. Deviation of the genotype frequencies in the controls from those expected under Hardy- Weinberg Equilibrium (HWE) was assessed by ⁇ 2 test (1 d.f.), or Fisher's exact test where an expected cell count was ⁇ 5.
  • SNP genotype and disease status were primarily assessed using the allelic 1 d.f. test or Fisher's exact test where an expected cell count was ⁇ 5.
  • the risks associated with each SNP were estimated by allelic, heterozygous and homozygous odds ratios (OR) using unconditional logistic regression, and associated 95% confidence intervals (CIs) were calculated in each case.
  • Patterns of risk for associated SNPs were investigated by logistic regression, coding the SNP genotypes according to additive, dominant and recessive models. Models were then compared by calculating the Akaike information criterion (AIC) and Akaike weights for each mode of inheritance. Associations by site (colon/rectum), MSI status, family history status (at least one first-degree relative with CRC), gender and age at diagnosis (stratifying into two groups by the median age at diagnosis) were examined by logistic regression in case-only analyses, using all cases from replication phases for whom the clinico-pathological variable being tested was available.
  • AIC Akaike information criterion
  • Results for gender and age at diagnosis were based on all case series apart from London Phase 1, VCQ58 and FCCPS; for site on data from London Phase 2, Edinburgh Phases 1 and 2, London Replication, SEARCH 5 Canada, DACHS and Kiel; for family history status and MSI status on London Phase 2 and London Replication.
  • the combined effect of each pair of loci identified as associated with CRC risk was investigated by logistic regression modelling and evidence for interactive effects between SNPs assessed by likelihood ratio test.
  • the OR and trend test for increasing numbers of deleterious alleles was estimated based on the London and Edinburgh Phase 2 data by counting two for a homozygote and one for a heterozygote.
  • VIOXX® colorectal cancer trial, United Kingdom KASPar patients following potentially curative therapy (VICTOR) 2
  • Table 24 SNPs associated with CRC in the meta-analysis of Phases 1 and 2 of the GWAS (P ⁇ 10 "5 ). Also shown are the individual study P- values and odds ratios (with associated 95% confidence intervals).
  • Cronin MT Fucini R V, Kim S M, Masino R S, Wespi R M and Miyada C G (1996) Cystic Fibrosis Mutation Detection by Hybridization to Light-Generated DNA Probe Arrays. Hum Mutat 7: pp 244-255.
  • Lam KS (1997) Application of Combinatorial Library Methods in Cancer Research and Drug Discovery. Anticancer Drug Des 12: pp 145-167.
  • SMAD7 influence colorectal cancer risk. Nat Genet 39, 1315-7 (2007). 8. Tomlinson, LP. et al. A genome- wide association study identifies colorectal cancer susceptibility loci on chromosomes 10pl4 and 8q23.3. Nat Genet 40, 623-30 (2008). 9. Tenesa, A. et al. Genome-wide association scan identifies a colorectal cancer susceptibility locus on I lq23 and replicates risk loci at 8q24 and 18q21. Nat Genet 40, 631-7 (2008). 10. Zanke, B. W. et al. Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24.

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Abstract

La présente invention concerne un procédé d'identification d'un individu qui présente un risque modifié de développement d'un cancer colorectal, le procédé comprenant la détection d'un polymorphisme mononucléotidique (SNP).
PCT/GB2008/050938 2007-10-16 2008-10-14 Marqueurs pour le cancer colorectal WO2009050507A1 (fr)

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Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003070082A2 (fr) * 2002-02-21 2003-08-28 Idgene Pharmaceuticals Ltd. Utilisation de polymorphismes de nucleotides simples dans le locus comt et dans les loci voisins pour determiner une predisposition a la schizophrenie, au trouble bipolaire, au cancer du sein et au cancer colorectal
US20060024715A1 (en) * 2004-07-02 2006-02-02 Affymetrix, Inc. Methods for genotyping polymorphisms in humans
WO2006104370A1 (fr) * 2005-04-01 2006-10-05 Samsung Electronics Co., Ltd. Snp multiple pour diagnostiquer le cancer colorectal, micromatrice et trousse le comprenant, et procede de diagnostic du cancer colorectal l’utilisant

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003070082A2 (fr) * 2002-02-21 2003-08-28 Idgene Pharmaceuticals Ltd. Utilisation de polymorphismes de nucleotides simples dans le locus comt et dans les loci voisins pour determiner une predisposition a la schizophrenie, au trouble bipolaire, au cancer du sein et au cancer colorectal
US20060024715A1 (en) * 2004-07-02 2006-02-02 Affymetrix, Inc. Methods for genotyping polymorphisms in humans
WO2006104370A1 (fr) * 2005-04-01 2006-10-05 Samsung Electronics Co., Ltd. Snp multiple pour diagnostiquer le cancer colorectal, micromatrice et trousse le comprenant, et procede de diagnostic du cancer colorectal l’utilisant

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
DATABASE NCBI [online] 7 March 2003 (2003-03-07), ANONYMOUS, XP002509360, retrieved from HTTP://WWW.NCBI.NLM.NIH.GOV/SNP/SNP_REF.CGI?RS=6533603 Database accession no. rs6533603 *
SHIVAPURKAR NARAYAN ET AL: "Deletions of chromosome 4 occur early during the pathogenesis of colorectal carcinoma", HUMAN PATHOLOGY, vol. 32, no. 2, February 2001 (2001-02-01), pages 169 - 177, XP002509359, ISSN: 0046-8177 *
ZANKE BRENT W ET AL: "Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24", NATURE GENETICS, vol. 39, no. 8, August 2007 (2007-08-01), pages 989 - 994, XP002509358, ISSN: 1061-4036 *

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