WO2010083880A1 - Prognosis of breast cancer patients by monitoring the expression of two genes - Google Patents
Prognosis of breast cancer patients by monitoring the expression of two genes Download PDFInfo
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- WO2010083880A1 WO2010083880A1 PCT/EP2009/050643 EP2009050643W WO2010083880A1 WO 2010083880 A1 WO2010083880 A1 WO 2010083880A1 EP 2009050643 W EP2009050643 W EP 2009050643W WO 2010083880 A1 WO2010083880 A1 WO 2010083880A1
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Definitions
- the present invention is related to a minimal gene signature providing useful information by molecular methods based on nucleic acid or on protein levels on breast cancer recurrence.
- BRCA1 is a tumor suppressor gene that is involved in DNA repair and cell cycle control, which are both important for the maintenance of genomic stability.
- BRCA2 is involved in the development of breast cancer and plays a role in DNA repair, while, unlike BRCA1 , it is not involved in ovarian cancer.
- Other genes have been linked to breast cancer, for example c-erb-2 (HER2) and p53 (Beenken et al., 2001 ). Overexpression of c-erb-2 (HER2) and p53 have been correlated with poor prognosis.
- the diagnosis of breast cancer requires histopathological proof of the presence of the tumor.
- histopathological examinations also provide information about prognosis and selection of treatment regimens. Prognosis may also be established based upon clinical parameters such as tumor size, tumor grade, the age of the patient, and lymph node colonization by tumor cells.
- Diagnosis and/or prognosis may be determined to varying degrees of effectiveness by direct examination of the outside of the breast, or through mammography or other X-ray imaging methods. The latter approach is not without considerable social and personal costs, however.
- MammaPrint® a gene expression profiling test system for breast cancer prognosis, based on cDNA microarray analysis for more than 70 genes, determined in fresh or frozen breast cancer biopsies, based on the study of van 't Veer, published in (van 't Veer et al., 2002). Even though this test is for physicians' use only, it has nevertheless to be carried out on special instrumentation, such as a DNA Bioanalyzer/microarray scanner. This represents a major drawback, since the result can only be provided by large hospitals or companies who developed means and standard procedures to carry out such a complex analysis. From the above, the advantages of the present invention based on the predictive prognostic value of the analysis of the expression of only two genes, can be easily understood.
- the detection comprises measuring a signal directly related to the gene(s) expression in said sample, acquiring the signal and evaluating the risk of cancer recurrence of a breast cancer patient by:
- a signature score for CyclinG2 gene expression values alone or for, preferably, both CyclinG2 and Sharpi expression values in the unknown sample
- the detection may be carried out by molecular and/or immunological means, where by molecular means are meant assays based on nucleic acids such as PCR, microarray analysis or Northern-blot.
- the method further comprises statistical analysis of the signal through the following steps:
- the invention further provides for a kit to evaluate CyclinG2 expression alone or in combination with Sharpi and determine the risk of cancer recurrence in a sample from a breast cancer patient, said kit preferably comprising: - a CyclinG2-specific reagent, preferably an oligonucleotide consisting in a oligonucleotide comprising at least a 13-mer oligonucleotide derived from
- Sharpi -specific reagent preferably an oligonucleotide consisting in an oligonucleotide comprising at least a 13-mer oligonucleotide derived from SEQIDNO:2 or its complementary sequence;
- the kit may further comprise as reference standards, CyclinG2 and Sharpi standard expression controls High and Low, as expression values or as nucleic acid samples. Said expression values or nucleic acid samples are preferably derived respectively from a non metastatic breast cancer cell line and/or from a highly metastatic cell line.
- Mutant-p53 expression promotes TGF ⁇ pro-migratory responses.
- A Western blot of H1299 cell lysates: parental, i.e., lacking p53 expression (null), or mutant-p53 (p53 R175H). The TGF ⁇ signaling cascade is similarly active in both cell lines, as monitored by Smad3 phosphorylation (P-Smad3). Lamin-B is a loading control.
- B Effect of TGF ⁇ (5ng/ml of TGF ⁇ for 24 hrs) on the morphology of H1299 cells.
- C Wound healing assays of H1299 cells showing the effects of mutant-p53 on TGF ⁇ driven migration. Pictures were taken 30 hours after scratching the cultures.
- H1299 cells were seeded on transwell membranes. When indicated, cells were treated with TGF ⁇ (4 ng/ml). The graph show the number of cells migrated through the transwell after 16 hrs. Only H1299 reconstituted with p53R175H cells acquire the ability to migrate in response to TGF ⁇ . Figure 2. Mutant-p53 is required for TGF ⁇ -driven invasion and metastasis in breast cancer mda-mb-231 cells.
- C Assay for invasive activity of MDA-MB-231 cells embedded in a drop of matrigel. Panels show pictures of the same field at different time points. Dotted lines highlight the edges of the drop. Only control cells are able to evade from the Matrigel® (arrows). This process is dependent on TGF ⁇ signaling as it is blocked by treatment with the TGF ⁇ RI inhibitor SB431542 (5 ⁇ M). MDA shp53 cells are impaired in matrix degradation and evasion.
- MDA-MB-231 cells display spindle shape in 3D culture conditions, once embedded in Matrigel® (top panel). Arrowheads indicate lamellipodia protrusions.
- MDA shp53 formed clusters of adherent, cobble-stone shaped cells
- E and F SCID mice were injected in the fat pad with MDA shGFP or MDA shp53 cells.
- E The rate of primary tumor growth was similar between the two cell populations.
- F Number of mice scored positive for lymphonodal metastasis.
- Kaplan-Meier curves show the probability to remain free of lung (left) and bone (right) metastasis for MSK samples (Minn et al., 2005) stratified according to the minimal signature.
- the minimal signature has a statistically significant predictive power for both organ-specific metastasis events.
- Minimal signature template is obtained by measuring the expression levels of CyclinG2 alone or preferably in combination with Sharpi in a population of tumor samples from patients with known clinical history.
- a template is calculated for each different assay used to determine CyclinG2 and
- CyCMGi ⁇ means and sta ndard deviations of CyclinG2 and preferably Sharpi expression levels in the population or dataset.
- the expression levels of CyclinG2 and Sharpi in two cell lines, BT20 (ATCC # HTB-19) and MDA-MB-436 (ATCC # HTB-130), representative for non-invasive and metastatic breast cancers, or other representative high and low standard expression controls, are preferably added to the population values of the template. Standard expression controls
- the signature score quantifies the differences between the CyclinG2 and preferably also Sharpi expression values in the unknown samples as compared to the template.
- TCTy-ch T n T G ⁇ 2 Sig s nature score for Cy JclinG2 and SharpVi in combination, where jcf*TM" "1 , x GydmG2 are the expression levels of Sharpi and CyclinG2 in the unknown sample / and ⁇ Sh ⁇ , ⁇ CycbnG2 , ⁇ Sh ⁇ rp ⁇ and ⁇ CycbnG2 define the template.
- the signature score is calculated as follows: where xf ychnG2 ⁇ s the expression levels of CyclinG2 in the unknown sample / an ⁇ i ftCy C tnG2 an ⁇ ⁇ Cy C knG2 ⁇ fj ⁇ ⁇ 0 temp
- Recurrence is defined as the development a breast cancer related metastasis
- breast cancer (more commonly to lung or bones) or breast cancer relapse within a period of 12 years from primary tumor surgery.
- Assay controls "assay controls" as known by the skilled man, evaluate the reliability of signal measure and acquisition by which the assay can be trusted to provide consistent results.
- a positive "assay control" for PCR is a known mix of nucleic acids where the PCR with the primers used, is expected to give the amplification of a DNA fragment of expected length.
- Internal expression controls the term is used, generally, to indicate housekeeping gene expression controls.
- the present invention is based on the experimental evidence that mutant alleles of p53 cooperates with TGF ⁇ , sustaining its pro-invasive and malignancy responses.
- mutant-p53 expression is required for invasion in vitro and for metastatic spread in vivo, highlighting a previously uncharacterized connection between these two pathways in breast cancer progression.
- the pro-invasive pathway activated by TGF ⁇ in a mutant p53 manner involves the down-regulation of the CyclinG2 and Sharpi genes whose lower expression levels correlates with a pro-invasive behavior of breast cancer and thus with a higher risk of cancer recurrence.
- This invention shows that CyclinG2 alone or CyclinG2 together with Sharpi , henceforth Minimal Signature (MS), have predictive power comparable to more complex gene set predictors. Due to the small number of genes involved in this evaluation, the present invention can be carried out by commonly used techniques and simple PCR apparatuses.
- the sample may be a breast cancer biopsy or a lymph node and either the tissue section or the nucleic acids, preferably the mRNA or cDNA isolated from such a sample.
- the minimal signature template is prepared by collecting gene expression data (i.e. CyclinG2 and, preferably also Sharpi ) from a population of patients whose clinical data and survival times at 5-12 years are known.
- the detection of one or preferably the two markers genes in the unknown sample is preferably carried out, at the same time and with the same reagents, in a control for the High expression level Standard of each of the genes (control High CyclinG2 and control High Sharpi ) and in a control for the Low expression (control Low CyclinG2 and control Low Sharpi ).
- Standard expression controls High and Low may be either derived from known patients or from cell lines that are representative for non-invasive or metastatic breast cancers (e.g., BT20 or MDA-MB-436) respectively.
- BT20 ATCC # HTB-19
- MDA-MB-436 ATCC # HTB-130
- BT20 expresses high levels of both genes, and, conversely, in MDA-MB-436 Sharpi and CyclinG2 are down-regulated.
- these two cell lines may provide easy-to- obtain High (BT20) and Low (MDA-MB-436) standard expression controls for the proposed method.
- at least one internal expression control for normalization purposes is measured in the same reaction.
- the selection of the internal expression control depends on the experimental technique used for monitoring the expression levels; normalization of the expression data may be based on computational methods (as scaling to average expression levels of all genes or quantile normalization) when using microarrays or on the expression levels of internal controls for molecular techniques based on nucleic acid, i.e. PCR or Northern-blot. Housekeeping genes commonly used to this purposes, for example in PCR, are selected among GAPDH, ⁇ -actin etc., which are constitutively expressed. For immunodetection based methods, internal controls will be preferably selected among LaminB or GAPDH immunoreactivity.
- a positive assay control for PCR is a known mix of nucleic acids where the PCR with the primers used, is expected to give the amplification of a DNA fragment of expected length.
- Measurement of the CyclinG2 and/or the Sharpi gene expression levels are assessed by any known state-of-the-art method, for example by molecular means based on molecular selection (i.e. selective amplification or hybridization) and / or by immunological means.
- Molecular selection i.e. selection by sequence specific hybridization with sequence specific probes or primers for CyclinG2 and/or Sharpi
- a separation step of the polynucleotide molecules targeted and/or amplified on the basis of the molecular weight, followed by quantification, for example by densitometry or by visual inspection, then by data normalization with any state-of-the-art computational method for example by linear scaling or non- linear normalization, and, preferably, by comparison with standard expression controls.
- comparison of the sample values with the minimal signature template is carried out by calculating the signature score. More in general however, the invention is based on the definition that, when the expression levels of CyclinG2, alone or preferably in combination with Sharpi gene in a sample, define a signature score which is lower than zero, this represents an indication that there is an increased risk of (breast) cancer recurrence.
- Statistical analysis to compare and/or differentiate an individual having one phenotype (for example an unknown sample) from other individuals having a second phenotype (for example the minimal signature template) is preferably used. Preferably this is carried out by a software.
- the method of the invention comprises a step b) carried out by a software running on a computer, which retrieves the stored template, quantifies the signature score of the sample through the marker(s) expression level signal(s) and assigns the unknown sample to High or Low minimal signature groups (as defined in step b) above). More preferably, the analysis of the signals (expression data) which have been acquired (according to step a) above) is carried out through the following additional steps:
- data rescaling on the basis of the standard expression controls, for example by linear or non-linear scaling.
- the template is retrieved, the signature score of the sample is calculated and the unknown sample is assigned to minimal signature High or Low groups (as defined in step c) ) above.
- the signature template is stored on a computer, or on computer readable media, and the software is used in prognosis-correlated signatures, the signature template is compared to the signature score from the sample.
- the expression levels of one or both the 2 marker genes in the sample are compared to the distribution of the expression levels of the same genes in the minimal signature, as determined from a pool of samples from patients with known prognosis (i.e., a pool of numerically suitable samples usually comprised from at least 50 to 100) comprising samples from patients or, alternatively or in addition, from cell lines that are representative for non-invasive and metastatic breast cancers.
- the unknown sample is classified as having a good prognosis for cancer recurrence if the levels of expression of one or both the 2 marker genes determine a signature score higher than zero. Conversely, unknown sample whose signature score is lower than zero are classified by the software as from patients having a poor prognosis.
- the method is preferably carried out by a software, the method is not limited to this embodiment: in fact the assignment to the High and Low expression group may be also carried out by visual inspection of the sample absolute expression signal, in the presence of the controls known by the skilled man, and by visually or numerically comparing this to the High and Low signature template (or standard expression controls as defined above).
- the signal related to the expression levels may be normalized e.g. by using different techniques, such as the average expression level of a set of control genes.
- markers expression level are normalized by the mean or median level of expression of a set of control markers (internal expression controls are, for nucleic acid based assays: GAPDH or ⁇ -Actin; for immunologically based assays: GAPDH and LaminB).
- the normalization is accomplished by standardization of the marker levels.
- the expression level data may be transformed in any convenient way, but, preferably, the expression signals are log transformed before normalization and comparison are carried out. Normalized values are then compared to the minimal signature template, which is composed of the normalized and/or transformed expression levels of the same marker genes, collected using the same experimental technique and protocols from a suitable pool of tumor patients with known clinical follow-up and from different breast cancer cell lines representative for non-invasive and metastatic breast cancers (e.g., BT20 and MDA-MB-436, respectively).
- the expression level of each of the markers may be normalized by the mean or median expression level across all of the genes represented on the microarray, including any non-marker (i.e. non CyclinG2 and non Sharpi ) genes.
- measurements of the expression levels can be carried out by any known method: molecular means comprises for example PCR (standard or Real- Time), Northern blot or microarray analysis. By Northern blot, total RNA samples are separated by electrophoresis according to the size and hybridization is carried out with labeled probes specific for the CyclinG2 and /or Sharpi .
- PCR or RT-PCR comprises as a preliminary step, the reverse transcription of a RNA sample in cDNA, can be carried out by using PCR primers identified from the published sequence of the CyclinG2 and Sharpi by standard sequence analysis with known and available software, for example by Primer3 (http://primer3.sourceforge.net).
- Preferred CyclinG2 and Sharpi forward and reverse primers for the PCR-based molecular method of the invention are shown in the following table comprising PCR primers also for amplification of preferred internal control genes:
- the method of the invention has been validated in the following breast cancer microarray datasets:
- Classification within one of the two groups of values with either high or low simultaneous expression scores of Sharpi and CyclinG2 is preferably carried out by summarizing the standardized expression levels of Sharpi and CyclinG2 into a combined score with zero mean.
- Tumors are classified as minimal signature Low if the combined score is negative and as minimal signature High if the combined score is positive:
- Sharp-l _ Sharp-l CyclmGl _ " CychnG2 minimal signature Low ⁇ ⁇ — " r ⁇ Shra ⁇ rp--,l + — “ . n Cy.c.l,m. ⁇ G,2 ⁇ 0
- Sharp-l _ Sharp-l CychnGl _ " CychnG2 minimal signature High ⁇ ⁇ — " r ⁇ Shra ⁇ rp--,l + — “ . n Cy.c.h, ⁇ nG,l > 0
- the present invention relates to a method for analyzing a breast cancer microarray dataset with the expression values of CyclinG2 alone or in combination with Sharpi .
- the prognostic method of the invention has been demonstrated, strikingly, to be highly predictive for breast cancer recurrence in the group expressing low levels of the minimal signature which displays a significant higher probability to develop recurrence when compared to the "High" group (p-values ranged from 0.02 to 3E-05, depending on the datasets) when tested using the univariate Kaplan-Meier survival analysis.
- a further advantage of the method of the present invention is that the expression of CyclinG2 and Sharpi are statistically correlated to the risk of distant metastasis to both bone and lung, and thus are independent from the site of secondary tumor formation.
- the method of the present invention can be based on any one of the following techniques for gene expression analysis, such as:
- the CyclinG2 detecting reagent is a CyclinG2- specific oligonucleotide, consisting in an oligonucleotide comprising at least a 13-mer oligonucleotide derived from SEQIDNO:1 or its complementary sequence.
- an anti-CyclinG2 alone or in combination with
- the specific detecting reagent is selected from the group consisting of: a Sharpi specific oligonucleotide, consisting in an oligonucleotide comprising at least a 13-mer oligonucleotide derived from SEQIDNO:2 or its complementary sequence, or an anti-Sharp1 specific antibody.
- a further embodiment of the invention is a kit for evaluating a breast cancer patient's risk of cancer recurrence, comprising CyclinG2 and preferably also Sharpi gene expression specific detection means, i.e. CyclinG2- specific oligonucleotides or probes, consisting in poly- or oligonucleotide comprising at least a 13-mer oligonucleotide derived from SEQIDNO:1 or its complementary sequence, and preferably Sharpi -specific oligonucleotide, consisting in poly- or oligonucleotide comprising at least a 13-mer oligonucleotide derived from SEQIDNO:2 or its complementary sequence.
- CyclinG2- specific oligonucleotides or probes consisting in poly- or oligonucleotide comprising at least a 13-mer oligonucleotide derived from SEQIDNO:1 or its complementary sequence
- Sharpi -specific oligonucleotide consist
- the invention is related to a kit for evaluating the expression of CyclinG2 alone or in combination with Sharpi in a sample from a breast cancer patient comprising at least a CyclinG2- specific reagent, preferably an oligonucleotide comprising at least a 13-mer derived from SEQIDNO:1 or its complementary sequence; preferably also a Sharpi -specific reagent, preferably an oligonucleotide comprising at least a 13-mer derived from SEQIDNO:2 or its complementary sequence; instructions for analysing an unknown sample specifying the criteria for assignment of the unknown sample measurement to a minimal signature High or Low group as defined above.
- the kit may further comprise as standard expression controls, CyclinG2 and Sharpi expression controls High and Low, i.e. CyclinG2 and Sharpi expression values measured in the cell lines BT20 and MDA-MB-436, respectively and dilution or assay buffers.
- Specific reagents, useful for each of the gene expression detection methods used, may be commercially available reagents, or custom made, provided that they are specific for CyclinG2 and/or Sharpi .
- Antibodies either preferably purified polyclonal or monoclonal, or oligonucleotides may be preferably labeled with fluorochromes, chemiluminescent labels or chromogens; polynucleotides, can be used in Northern Blot after having been labeled, for example with 32 P. Specific antibodies may be directly labeled or detected by using a secondary labeled antibody.
- the kit further comprises instructions for use reporting the criteria for assigning each sample measurement to a high or low minimal signature where low minimal signature correlates with an increased risk of breast cancer recurrence, or preferably.
- the above specified calculation are carried out by software.
- the kit may comprise assay controls, consisting in a negative and a positive sample, or reagents to detect internal expression controls and, optionally, nucleic acid extraction reagents.
- the PCR primer pair for CyclinG2 expression level detection are the following: CyclinG2 (forward): 5' CCTCCCAGTGATCAAGAGTGC 3 ' CyclinG2 (reverse): 5' TCCCTCCTCCCCAAAGTAGC 3'; for Sharpi (forward): 5' GCATGAAACGAGACGACACC 3' and (reverse): 5'
- RT-PCR Semi-quantitative PCR
- RT-PCR Semi-quantitative PCR
- a densitometric analysis or visual inspection provides for the expression level of each gene and a comparison with standard expression controls is carried out to define a low expression group for CyclinG2 alone or in combination with Sharpi .
- the kit comprises means for the immunological detection of the CyclinG2 and Sharpi expression, such as specific antibodies and relevant controls.
- the prognostic indication for CyclinG2 and Sharpi represents one of the most significant index for the physician, who has however to complete the prognostic evaluation with other known prognostic and predictive factors in breast cancer, such as age, tumor size, axillary lymph node status, histological tumor type, pathological grade and hormone receptor status.
- the minimal signature results a significant predictor of recurrence-free survival, adding new prognostic information beyond the one provided by the standard clinical predictors.
- the minimal signature adds prognostic value not only to the multivariate model but also to any model calculated using any single clinical predictor. Indeed, the difference between the residual deviance of the model obtained using a single clinical variable plus the minimal signature (e.g., nodal status + minimal signature) and the residual deviance of the model obtained using only a clinical variable, is significant for each clinical predictor.
- the method of the invention is particularly useful to gain prognostic indication for patients representing more than 50% of the breast cancer patients where by traditional prognostic markers is confidentially assigned either an obviously poor or a clearly good outcome.
- a particularly relevant point of the present method is that it usefully applies to tumors classified as intermediate (grade 2) by the Nottingham scale which represent the majority of tumors and whose prognosis is uncertain (Ivshina et al., 2006).
- grade 2 tumors of multiple independent datasets the minimal signature stratified grade 2 samples into two groups with outcomes comparable to grade 1 and grade 3, respectively.
- the resolution achieved represents thus a preferred embodiment of the method of the invention as applied to the stratification of breast tumor patients classified as Grade 2 according to Nottingham scale for a more correct classification and possibly, assignment to different therapeutic categories or clinical trials.
- H1299 and the derived cell line expressing mutant p53 R175H are a gift of G. Blandino (Strano et al., J Biol Chem 2002).
- H1299 non-small lung carcinoma cells were maintained in DMEM, 10% serum, 1 mM glutamine. TGF ⁇ treatments were done in DMEM 0.2% serum (TGF ⁇ was provided from Peprotech).
- p53R175H H1299 cells express stably transfected plasmids coding for ponasterone-inducible cDNAs for a mutant p53R175H allele. p53 expression was induced by incubating cells with Ponasterone-A (Alexis, 3 mM) for 16 hours before treatments.
- MDA-MB-231 (ATCC # HTB-26) were maintained in a 1 :1 mixture of DMEM and F12 (DMEM/F12) supplemented with 10% serum, 2 mM glutamine.
- DMEM/F12 DMEM/F12
- 10% serum fetal calf serum
- 2 mM glutamine 10% serum, 2 mM glutamine.
- TGF ⁇ treatments cells were serum starved for 24 hours and then treated with TGF ⁇ i (5 ng/ml) in DMEM/F12 without serum.
- siRNA small interfering RNA
- shRNAs small hairpin RNA or short hairpin RNA
- Small-hairpin-RNA (shRNA) expression constructs were generated by cloning annealed DNA oligonucleotides in pSUPER-retro-puro (OligoEngine). All plasmids were controlled by sequencing. For stable knock-down, retroviral particles were obtained by transfecting plasmids for expression of shRNAs (pSuperRetro) and VSV envelope in 293gp (gift from M. Tripodi) with calcium-phosphate. Two days after transfection, surnatants were collected, filtered and used to infect of MDA-MB-231. After selection for puromycin resistance, transduced cells were verified for downregulation of the target protein. Migration and invasion assays
- H1299 cells were plated in 6-well plates and cultured to confluence. Cells were scraped with a p200 tip (time 0), transferred to low serum and treated as described. Transwell migration assay were performed in 24 well PET inserts (Falcon 8.0 mm pore size) for migration assays.
- MDA-MB-231 cells were plated in 10 cm dishes, transfected with siRNA and, after 8 hours, serum starved overnight. Then, 50000 or 100000 cells were plated in transwell inserts (at least 3 replicas for each sample) and either left untreated or treated with TGF ⁇ i (5 ng/ml). For H1299, cells were plated in the transwell in 10% serum but then changed to 0.2% serum.
- shGFP- or shp53-MDA-MB-231 cells (1 x 10 6 cells/mouse) were unilaterally injected into the mammary fat pad of SCID female mice, age-matched between 5 and 7 weeks. After six weeks, mice were sacrificed and examined for metastases to lymph nodes. Macroscopic metastases to other organs were infrequent (liver, lung, peritoneum). Tumor growth in the injected site was monitored by repeated caliper measurements. For lung colonization assays, cells were resuspended in 100 ml of PBS and inoculated in the tail vein of SCID mice. Four weeks later, animals were sacrificed and lungs removed for the subsequent histological analysis. Histology and immunohistochemistry
- Tissues for histological examination were fixed in 4% buffered formalin, dehydrated and embedded in paraffin by standard methods.
- RNA per sample 10 mg were loaded and separated in a 6% formaldehyde/ 1 % agarose gel, blotted by upward capillary transfer onto GeneScreenPlus (PerkinElmer) and UV crosslinked.
- Membranes were pre-hybridized 5 hrs at 42°C with ULTRAhyb-Oligo solution (Ambion), and hybridized with 32 P-labeled DNA probes o.n. at 42 0 C. Membranes were washed at 68 °C with 2xSSC/0,5%SDS solutions and exposed for autoradiography. All probes were obtained by random- primer amplification.
- CyclinG2 and Follistatin probe templates were obtained from RZPD EST (HU3_p983B0120D, HU3_p983D0140D2 and RZPD EST HU3_p983D01 13D2 respectively).
- GPR87 and ADAMTS9 probes were obtained cloning RT-PCR products. All probes were validated by sequencing.
- MDA shGFP and shp53 cells were serum-starved for 24 hours, and then either left untreated or treated with TGF ⁇ i (5 ng/ml for 3 hours) in DMEM/F12 without serum.
- TGF ⁇ i 5 ng/ml for 3 hours
- Four replicas were prepared for each of the four conditions (untreated shGFP, TGF ⁇ -treated shGFP, untreated shp53, TGF ⁇ -treated shp53) for a total of 16 samples.
- Total RNA was extracted using Trizol (Invitrogen) according to the manufacturer's instructions. Sample preparation for microarray hybridization was carried out as described in the Affymetrix GeneChip® Expression Analysis Technical Manual. Briefly, 15 ⁇ g of total RNA were used to generate double- stranded cDNA (Invitrogen).
- Biotin-labeled cRNA was performed using the BioArrayTM HighYieldTM RNA Transcript Labeling Kit (ENZO Biochem, New York, NY). The length of the cRNA fragmentation was confirmed using the Agilent 2100 Bioanalyzer (Agilent Technologies). Four biological mRNA replicates for each group were hybridized on Affymetrix GeneChip® Human Genome HG- U133 Plus 2.0 arrays.
- SAM is a statistical technique for finding significant genes in microarrays while controlling the False Discovery Rate (FDR). SAM uses repeated permutations of the data to determine if the expression level of any genes is significantly related to the physiological state and the significance is quantified in terms of q-value (Storey, 2002), i.e. the lowest False Discovery Rate at which a gene is called differentially expressed.
- TGF- ⁇ target genes To identify genes whose expression is modified by TGF ⁇ , we compared the expression profile of TGF ⁇ treated MDA-MB-231 cells (either shGFP or shp53) with their untreated controls and selected those transcripts whose q-value was ⁇ 0.1. This selection was further refined setting the lower limit for TGF ⁇ fold induction (or reduction) to 1.5. Using this combined filter, we were able to identify 447 genes differentially regulated between the untreated and TGF ⁇ treated MDA- MB-231 samples.
- Example 1 Effects of mut.ant.-p53 on the cellular response to TGF ⁇ .
- p53-null H1299 cells stably reconstituted with inducible expression vectors coding for the hot-spot p53R175H mutant allele. This cell line retained similar responsiveness to TGF ⁇ compared to parental H1299, as judged by activation of P-Smad3 ( Figure 1 A).
- TGF ⁇ treatment of H1299 cells bearing p53R175H caused a strikingly morphology change, as cells shed their cuboidal epithelial shape and acquired a more mesenchymal phenotype, characterized by a number of dynamic protrusions, such as filopodia and lamellipodia ( Figure 1 B). These were not present in parental cells or in cells reconstituted with wild-type p53 ( Figure 1 B and data not shown).
- a wounding assay in which cells are induced to disrupt cell-cell contacts, polarize and migrate into a wound created by scratching confluent cultures with a pipette tip.
- Example 2 Mutant-p53 and TGF ⁇ jointly control cell shape and invasiveness of breast cancer cells in vitro.
- endogenous mutant-p53 p53R280K
- Mutant-p53 expression plays a crucial role in canalizing TGF ⁇ responsiveness for efficient metastatic spread in vivo.
- Multiple evidences indicate that the metastatic spread of MDA-MB-231 cells in vivo is under control of autocrine TGF ⁇ (Arteaga et al., 1993; Bandyopadhyay et al., 1999; Deckers et al., 2006; Padua et al., 2008).
- shGFP- or shp53- MDA-MB-231 cells into the mammary fat pad of immunocompromized mice.
- mice were sacrificed and examined for presence of metastatic lesions.
- mutant-p53 in invasiveness in vivo, we injected control and shp53-MDA-MB-231 intravenously into nude mice. Using two independent clones, we found that depletion of mutant-p53 had a remarkable impact on lung colonization, with overt reduction of metastatic nodules in number and size ( Figures 2G-2I). Thus, mutant-p53 expression plays a crucial role in canalizing TGF ⁇ responsiveness for efficient metastatic spread.
- Example 4 Identification of the gene set co-regulated by mut.ant.-p53 and TGF ⁇ . We next sought to investigate the specific gene expression program by which mutant-p53 and TGF ⁇ control invasion and metastasis.
- TGF ⁇ transcriptomic profile of control and mutant-p53 depleted MDA-MB-231 cells we compared the TGF ⁇ transcriptomic profile of control and mutant-p53 depleted MDA-MB-231 cells. We found that TGF ⁇ potentially regulates more than 400 genes. The large majority of them were expressed independently from the presence of mutant p53.
- mutant-p53-independent targets several had been previously described as direct Smad targets, such as PAI1/SERPINE1, JunB and Smad7 (Massague and Gomis, 2006).
- multiple genes previously associated to a general epithelial "TGF ⁇ response classifier" were also found, including genes associated to lung or bone specific metastasis (ANGPTL4, NEDD9, IL 11 and CTGF) (Padua et al., 2008).
- the successful identification of these targets validated our procedure to identify novel genes that may play important roles in TGF ⁇ induced malignancy.
- we highlighted 147 genes previously implicated in cell movement, invasion or metastasis (Figure 3A and data not shown).
- TGF ⁇ needs the presence of mutant p53 to exploit its pro-metastatic function; we therefore restricted our attention to a much smaller set of genes co- regulated by mutant-p53 and TGF ⁇ ; strikingly, this entailed only five genes: Sha ⁇ 1/DEC2/BHLHB3/BHLHE41, CyclinG2/CCNG2, ADAMTS9, Follistatin and GPR87 (see Figure 3B and 3C).
- this entailed only five genes: Sha ⁇ 1/DEC2/BHLHB3/BHLHE41, CyclinG2/CCNG2, ADAMTS9, Follistatin and GPR87 (see Figure 3B and 3C).
- Sharpi is an inhibitory basic helix-loop-helix resembling ID-proteins (i.e.
- CyclinG2 is considered an atypical "inhibitory" cyclin, but can also influence the dynamic of the microtubule cytoskeleton; interestingly, CyclinG2 is asymmetrically inherited during cell division, in virtue of its association with the centrosome surrounding the mother centriole (Arachchige Don et al., 2006).
- Example 5 Biological validation of the identified gene set in vitro. To functionally validate these genes as effectors of the mutant-p53/TGF ⁇ pathway, we carried out epistasis experiments testing if depletion of Sharpi or CyclinG2 could rescue TGF ⁇ induced migration in p53-depleted cells. As shown in Figure 3E, siRNA-mediated knockdowns of Sharpi or CyclinG2 restore TGF ⁇ dependent pro-migratory activities in shp53 MDA-MB-231 ( Figure 3E, compare lanes 3 and 4 with lane 2) Thus, these molecules antagonize TGF ⁇ proinvasive responses, acting as metastasis suppressors.
- Example 6 Prognostic validation of the gene set identified by statistical analysis and comparison with other gene sets.
- Breast cancer dataset To evaluate the prognostic value of Sharpi and CyclinG2, we collected 6 different datasets (Table 3). For each data set, we performed survival analysis to test if the minimal signature could classify patients into clinically distinct groups. Each dataset has been processed independently from the other to preserve the original differences among the various studies (e.g., patient cohort, microarray type, sample processing protocol, etc.).
- Table 3 reports the complete list of datasets and their sources.
- raw data e.g., CEL files
- CEL files were available for all samples. Detailed clinical information could be acquired for any analyzed sample.
- the datasets included both Affymetrix and dual-channel cDNA microarray platforms. Since all Affymetrix data were from the same HG-U133A platform, no method was needed to map probesets across various generations of Affymetrix GeneChip arrays.
- CEL files were available, expression values were generated from intensity signals using the RMA algorithm; values have been background adjusted, normalized using quantile normalization, and expression measure calculated using median polish summarization.
- EMC EMC
- MSK and NKI studies data were used as downloaded.
- the Agilent, Rosetta lnpharmatics array used for the NKI dataset has a single probe for CyclinG2 while does not contain any probe for Sharpi .
- Tumors were then classified as minimal signature Low if the combined score is negative and as minimal signature High if the combined score is positive:
- x ⁇ ha ⁇ , xf ydmG2 are the expression levels of Sharpi and CyclinG2 in sample / and fl s ⁇ fl ⁇ G2
- ⁇ Shmp - ⁇ and ⁇ qydmG2 are the estimated means and standard deviations of Sharpi and CyclinG2 calculated over the entire dataset. This classification was applied for Sweden, NCI and Uppsala studies based on expression values obtained from RMA, whereas for EMC and MSK expression values have been used as downloaded. In the case of EMC dataset, expression data have been Iog2-transformed.
- Table 4 Multivariate analysis of the risk of recurrence for the NCI dataset using a Cox proportional-hazards model
- Model 2 Multivariate analysis using clinical variables and the minimal signature.
- Table 5 Statistical comparison between models obtained using single clinical variables and models obtained adding the minimal signature.
- the minimal signature adds prognostic value not only to the multivariate model but also to any model constructed using any single clinical predictor.
- the difference between the residual deviance of the model obtained using a single clinical variable plus the minimal signature (e.g. tumor diameter+m/n/ma/ signature) and the residual deviance of the model obtained using only a clinical variable is significant for each clinical predictor.
- the matrigel chemoinvasion assay as a tool for dissecting molecular mechanisms.
- CyclinG2 is a centrosome-associated nucleocytoplasmic shuttling protein that influences microtubule stability and induces a p53-dependent cell cycle arrest.
- TGF-beta antibodies inhibit breast cancer cell tumorigenicity and increase mouse spleen natural killer cell activity. Implications for a possible role of tumor cell/host TGF-beta interactions in human breast cancer progression. The Journal of clinical investigation 92, 2569-
- the tumor suppressor Smad4 is required for transforming growth factor beta-induced epithelial to mesenchymal transition and bone metastasis of breast cancer cells. Cancer research 66, 2202-2209. Dudoit, S., Popper Shaffer. J., Boldrick, J. C. (2003). Multiple Hypothesis Testing in
- DEC1 negatively regulates the expression of DEC2 through binding to the E-box in the proximal promoter.
- TGFbeta primes breast tumors for lung metastasis seeding through angiopoietin-like 4.
- the head inducer Cerberus is a multifunctional antagonist of Nodal, BMP and Wnt signals. Nature 397, 707-710.
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US20200247861A1 (en) * | 2012-04-02 | 2020-08-06 | Modernatx, Inc. | Modified polynucleotides for the production of oncology-related proteins and peptides |
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US9035039B2 (en) * | 2011-12-22 | 2015-05-19 | Protiva Biotherapeutics, Inc. | Compositions and methods for silencing SMAD4 |
CN108064380A (en) * | 2014-10-24 | 2018-05-22 | 皇家飞利浦有限公司 | Use the prediction of the medical prognosis and therapeutic response of various kinds of cell signal transduction path activity |
RU2733697C1 (en) * | 2020-03-11 | 2020-10-06 | Федеральное государственное бюджетное научное учреждение "Томский национальный исследовательский медицинский центр Российской академии наук" (Томский НИМЦ) | Method for prediction of risk of developing distant metastases in patients with operable forms of breast cancer with metastases in regional lymph nodes |
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US20200247861A1 (en) * | 2012-04-02 | 2020-08-06 | Modernatx, Inc. | Modified polynucleotides for the production of oncology-related proteins and peptides |
WO2014006227A1 (en) * | 2012-07-06 | 2014-01-09 | Institut Gustave-Roussy | Simultaneous detection of cannibalism and senescence as prognostic marker for cancer |
US9726661B2 (en) | 2012-07-06 | 2017-08-08 | Institut Gustave-Roussy | Simultaneous detection of cannibalism and senescence as prognostic marker for cancer |
US10969380B2 (en) | 2012-07-06 | 2021-04-06 | Institut Gustave Roussy | Simultaneous detection of cannibalism and senescence as prognostic marker for cancer |
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