WO2014115779A1 - WT1 mRNAの発現量定量方法 - Google Patents
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Definitions
- the present invention relates to a new method for quantifying the expression level of human WT1 mRNA that can be used for diagnosis of cancer such as leukemia and solid cancer and determination of bone marrow transplantation timing.
- WT1 Wilms tumor gene-1
- Non-patent Document 2 The Wilms tumor-1 gene (Wilms tumor gene-1; hereinafter referred to as “WT1”) gene was identified as a causative gene of childhood Wilms tumor in 1990 by Call et al.
- WT1 mRNA is expressed not only in pediatric Wilms tumor but also in solid cancer cells such as gastric cancer cell lines, colon cancer cell lines, lung cancer cell lines, and breast cancer cell lines. It has been shown (Non-patent Document 2) that the WT1 gene is now considered to be a cancer-related gene related to many cancers as well as childhood Wilms tumor.
- Non-patent Document 1 Reported the expression of WT1 mRNA in K562 cells and CCRF-CEM cells (see Non-Patent Document 1), and Miwa et al. Reported acute myeloid leukemia (acute myeloid leukemia) by Northern blot analysis.
- AML acute myeloid leukemia
- Non-patent Document 5 the expression level of WT1 mRNA at the time of diagnosis is related to prognosis (Non-patent document 5), the expression level of WT1 mRNA is negatively increased once after treatment (Non-patent document 6), and It has been reported that the expression level of WT1 mRNA at the time of recurrence is higher than the expression level at the time of diagnosis (Non-patent Document 7).
- the WT1 gene is a new minimal residual disease in the treatment of AML. Since it is useful as a monitoring marker of (minimal residual disease, hereinafter also referred to as “MRD”), it has been conventionally sold as a pharmaceutical for in vitro diagnosis.
- MRD minimal residual disease
- Patent Document 1 As a method for measuring human WT1 mRNA, a competitive quantification method based on ⁇ -actin is conventionally known (Patent Document 1). However, in this measurement method, it is necessary not only to measure WT1 mRNA and ⁇ -actin mRNA individually, but also to perform a so-called two-step RT-PCR method in which an extension reaction is performed after reverse transcription reaction. Takes time.
- Patent Document 2 discloses a one-step RT-PCR method for WT1 mRNA.
- this measurement method is complicated because it is necessary to separately measure the expression level of the housekeeping gene for correcting the expression level of the WT1 gene.
- an object of the present invention is to provide a new WT1 mRNA quantification method that can be carried out simply and in a short time.
- the present invention aims to provide a new WT1 mRNA quantification method that enables simple and short-time implementation by simultaneously quantifying the expression levels of both human WT1 mRNA and housekeeping gene. .
- the inventors of the present invention have intensively studied to solve the above-mentioned problems.
- the reverse transcription reaction and elongation reaction of the target gene human WT1 gene (mRNA) and the correction gene housekeeping gene (mRNA) are performed.
- the present inventors have found that the expression level of the target human WT1RNA mRNA can be quantified in a short time and simply by proceeding simultaneously and continuously in the same container (1 step).
- the target gene can be obtained more easily and in almost the same time as compared with the two-step RT-PCR method in which the target gene and the correction gene are amplified separately. It was confirmed that it was possible to detect with high sensitivity.
- the present invention has been completed based on such knowledge, and includes the following embodiments.
- (I) Method for quantifying the expression level of human WT1 mRNA (I-1) A method for quantifying the expression level of human WT1 mRNA using a one-step RT-PCR method, comprising human WT1 mRNA and a housekeeping gene (mRNA) A method for quantifying the expression level of human WT1 mRNA, wherein the reverse transcription reaction and the extension reaction of are allowed to proceed simultaneously and continuously in the same container. (I-2) The method according to (I-1), wherein the housekeeping gene is GAPDH mRNA.
- (I-3) For PCR amplification of human WT1 mRNA, (A) A primer set consisting of a forward PCR primer consisting of the base sequence shown in SEQ ID NO: 3 and a reverse PCR primer consisting of the base sequence shown in SEQ ID NO: 4, or (b) a forward consisting of the base sequence shown in SEQ ID NO: 9
- (I-4) For PCR amplification of human WT1 mRNA, (A ′) a primer set consisting of a forward PCR primer consisting of the base sequence shown in SEQ ID NO: 3 and a reverse PCR primer consisting of the base sequence shown in SEQ ID NO: 4, and a probe consisting of a labeled base sequence shown in SEQ ID NO: 5 Or (b ′) a primer set consisting of a forward PCR primer consisting of the base sequence shown in SEQ ID NO: 9 and a reverse PCR primer consisting of the base sequence shown in SEQ ID NO: 10 and a labeled base sequence shown in SEQ ID NO: 11 The method described in (I-1) or (I-2) using the probe.
- (I-5) Primer set comprising PCR amplification of human WT1 mRNA and (c) a forward PCR primer consisting of the base sequence shown in SEQ ID NO: 6 and a reverse PCR primer consisting of the base sequence shown in SEQ ID NO: 7 or 12 The method described in (I-3) or (I-4).
- (II) Real-time PCR kit for quantifying the expression level of human WT1 mRNA (II-1) (a) Forward PCR primer consisting of the base sequence shown in SEQ ID NO: 3 and reverse PCR primer consisting of the base sequence shown in SEQ ID NO: 4 Or (b) a primer set consisting of a forward PCR primer consisting of the base sequence shown in SEQ ID NO: 9 and a reverse PCR primer consisting of the base sequence shown in SEQ ID NO: 10, A kit for real-time PCR for quantifying the expression level of human WT1 mRNA comprising (II-2) (a ′) a primer set consisting of a forward PCR primer consisting of the base sequence shown in SEQ ID NO: 3 and a reverse PCR primer consisting of the base sequence shown in SEQ ID NO: 4, and a labeled SEQ ID NO: 5 (B ′) a primer set consisting of a forward PCR primer consisting of the base sequence shown in SEQ ID NO: 9 and a reverse PCR primer
- (II-4) Further, (c ′) a primer set consisting of a forward PCR primer consisting of the base sequence shown in SEQ ID NO: 6 and a reverse PCR primer consisting of the base sequence shown in SEQ ID NO: 7 or 12, and a labeled SEQ ID NO:
- the method of the present invention it is possible to provide a method for quantifying the expression level of WT1 mRNA, which can be measured in a short time with simple operation and labor, compared to the conventional method for quantifying the expression level of WT1 mRNA. it can. Further, according to the method of the present invention, it is possible to detect with higher sensitivity than the measurement method using the conventional two-step RT-PCR method. That is, by using the method of the present invention or the kit for real-time PCR, the expression level of human WT1 mRNA can be quantified with high sensitivity in a simple and short time.
- the expression level of human WT1 mRNA quantified is a useful index for diagnosis of onset and recurrence of leukemia and solid cancer, judgment of prognosis, and determination of the timing of bone marrow transplantation.
- Example 1 which shows the GAPDH mRNA amplification curve at the time of amplifying GAPDH mRNA alone for the GAPDH RNA standard product of (1).
- Example 1 which shows the GAPDH mRNA amplification curve at the time of amplifying WT1 mRNA and GAPDH mRNA simultaneously.
- Example 2 Using 1-step RT-PCR that simultaneously amplifies WT1 mRNA and GAPDH mRNA as primers and probes, (A) the set shown in Table 8 (sequence set B) and (B) the set shown in Table 9 (comparison set), respectively. The results of agarose gel electrophoresis of the amplification product obtained by using this method are shown.
- the method of the present invention is a method for quantifying the expression level of human WT1 mRNA using a one-step RT-PCR method.
- the human WT1 gene to be measured by the present invention is a gene consisting of 3037 bp identified as a causative gene of childhood Wilms tumor as described above, and ⁇ Homo sapiens Wilms tumor 1 (WT1), transcript variant D, mRNA '' As registered with NCBI (NM_024426.4).
- the base sequence is shown in SEQ ID NO: 1 in the sequence listing.
- the test sample to be measured by the method of the present invention is not particularly limited as long as it contains the above-mentioned human WT1RNA mRNA, for example, human-derived cells, tissues, blood, sputum, feces, urine and other biological samples, A total RNA obtained by processing by a known method from a sample possibly containing WT1 mRNA, a sample enriched in mRNA, or the like can be used.
- the RNA sample can be used in an aqueous solution or in an adsorbed or immobilized state on an appropriate solid phase.
- the total RNA amount is suitably 0.01 ng to 1 ⁇ g per 100 ⁇ l of reaction solution.
- a housekeeping gene is a gene that is always expressed and present in any cell regardless of cell differentiation, has no essential function, but has an essential role in their survival, such as RNA synthase, energy Genes such as production system enzymes, ribosomal proteins, and cytoskeletal proteins can be exemplified. Specifically, genes such as GAPDH (glyceraldehyde-3-phosphate dehydrogenase), ⁇ -actin, ⁇ 2-microglobulin, and HPRT 1 (hypoxanthine phosphoribosyltransferase 1) can be mentioned.
- the housekeeping gene used in the present invention is preferably one that does not compete with the human WT1 gene to be measured for amplification by RT-PCR, for example, one that has low base sequence homology. GAPDH is preferred.
- GAPDH is a gene registered with NCBI as “Homo sapiens glyceraldehyde-3-phosphate dehydrogenase (GAPDH), mRNA” (NM_002046.3). The base sequence is shown in SEQ ID NO: 2 in the sequence listing.
- the reaction buffer used in the one-step RT-PCR method may be a water-soluble buffer suitable for the activity of an enzyme having reverse transcription activity,
- a buffer solution having a pH of 7 to 10, preferably pH 8 to 9, such as a Tris buffer can be mentioned.
- this buffer contains various ions necessary for the activity of an enzyme having a reverse transcription activity or a DNA polymerase.
- Na ions and K ions are added in a salt form in a concentration of 5 to 50 mM.
- Mg ions are added at 1-10 mM in salt form.
- an agent that promotes or stabilizes the activity of an enzyme having reverse transcription activity or a DNA polymerase such as a surfactant, bovine serum albumin (BSA), gelatin, and the like can be added as necessary.
- a ribonuclease inhibitor may be added to suppress degradation of RNA and RNA competitors in the sample.
- Enzymes with reverse transcription activity include avian osteoblastosis virus-derived reverse transcriptase (AMV), Rous-related virus-derived reverse transcriptase (RAV2), Moloney murine leukemia virus-derived reverse transcriptase (MMLV), and thermus thermo Examples include DNA polymerase (Tth) derived from Thermusthermophilus, DNA polymerase (Bca) derived from Bacillus cardotenax ⁇ ⁇ ⁇ , and derivatives thereof, among which Tth is most suitable for the present invention. Specific examples of Tth include Thermostable enzyme DNA polymerase derived from Thermus species Z05. These enzymes may be either purified and obtained from their original origin, or recombinant proteins produced by genetic engineering.
- AMV avian osteoblastosis virus-derived reverse transcriptase
- RAV2 Rous-related virus-derived reverse transcriptase
- MMLV Moloney murine leukemia virus-derived reverse transcriptase
- thermus thermo Examples include DNA polyme
- dNTP deoxynucleotide triphosphates
- the primer used for cDNA synthesis (reverse transcription reaction and extension reaction) from the target RNA is an oligonucleotide having at least a base sequence complementary to the base sequence of the target RNA, under the reaction conditions employed. It must be annealed to the target RNA. Examples of the length of the oligonucleotide include 6 to 100 nucleotides, preferably 10 to 30 nucleotides. Modified and / or labeled primers can also be used. The primer can be chemically synthesized by, for example, a known method. The primer used in PCR must be capable of amplifying DNA using at least cDNA derived from the target RNA as a template.
- the oligonucleotide has at least a base sequence complementary to the base sequence of the template cDNA and anneals to the cDNA under the reaction conditions employed.
- it is an oligonucleotide that functions as a primer for cDNA synthesis (reverse transcription reaction and extension reaction) from the target RNA and also functions as a primer for DNA using cDNA as a template.
- a primer set suitably used for reverse transcription, extension, and amplification of human WT1WT mRNA, which is the target gene of the present invention is composed of (A1) Forward primer and (A2) Reverse primer described in Table 1 below. Mention may be made of primer set A and primer set B consisting of (B1) Forward primer and (B2) Reverse primer described in Table 2. Tables 1 and 2 also show sequence-specific binding probes ((A3) Probe, (B3) Probe) used to detect human WT1 gene amplification products amplified with these primer sets. . Such a probe is preferably labeled in order to facilitate detection of the amplified product.
- primer sets that are preferably used to reverse-transcribe, extend, and amplify human GAPDH mRNA that is preferably used as a housekeeping gene in the method of the present invention are described in Table 1 below (a1) Forward Examples include primer set A comprising a primer and (a2) Reverse primer, and primer set B comprising (b1) Forward primer and (b2) Reverse primer described in Table 2.
- Tables 1 and 2 also show sequence-specific binding probes ((a3) Probe, (b3) Probe) used to detect human GAPDH gene amplification products amplified with these primer sets. . Such a probe is preferably labeled in order to facilitate detection of the amplified product.
- the probe labeling method includes an RI method and a non-RI method, but it is preferable to use a non-RI method.
- Non-RI methods include a fluorescent labeling method, a biotin labeling method, a chemiluminescence method, and the like, and the fluorescent labeling method is preferably used.
- the fluorescent substance is not particularly limited as long as it can bind to the base moiety of nucleic acid, but cyanine dyes (Cy ⁇ DyeTM series Cy3 and Cy5 etc.), rhodamine 6G reagent, N-acetoxy-N2-acetylaminofluorene and its iodine Derivatives can be used.
- RNA standard used in the present invention can be prepared by a known method. For example, “Proceedings of the National Academy of Sciences of the United States of America (Proc. Natl. Acad. Sci. USA), Vol.87, 275-2729 (1990)”, “Clinical Chemistry (Clin. Chem. ), Vol. 41, pp. 819-825 (1995) ”,“ Blood, Vol. 82, 1929-1936 (1993) ”, and the like.
- a promoter sequence serving as a reaction base point of an RNA synthetase for example, T7 RNA polymerase, is added to the double-stranded DNA sequence to be amplified to create a DNA sequence that serves as a template for RNA synthesis.
- RNA polymerase for example, T7 RNA polymerase
- double-stranded DNA containing an RNA promoter sequence and nucleoside triphosphate are added and reacted at 37 ° C. for 30 minutes to 2 hours, so that one complementary to the template DNA downstream of the RNA promoter. Synthesize single-stranded RNA.
- reaction operation and reaction conditions of the 1-step RT-PCR used in the present invention are not limited, but the following can be exemplified.
- a reaction solution containing cNTP, Mg salt, ribonuclease inhibitor, enzyme having reverse transcription activity, primer and the like is added and kept at 4 ° C. or less until the reaction starts.
- a test sample that can contain human WT1GAmRNA to be measured and a housekeeping gene (for example, GAPDH mRNA) are added and 50 to 70 ° C, preferably 55 to 65 ° C, 2 to 30 minutes, preferably 2 to 10 minutes.
- a DNA fragment derived from the target RNA is amplified by performing 2 to 50 cycles of a temperature cycle reaction comprising heat denaturation at 90 to 99 ° C., annealing reaction at 45 to 65 ° C., and DNA extension reaction at 60 to 80 ° C.
- a temperature cycle reaction comprising heat denaturation at 90 to 99 ° C., annealing reaction at 45 to 65 ° C., and DNA extension reaction at 60 to 80 ° C.
- primers used for the first and second stage PCR are added to the reaction vessel from the beginning, and the two stage PCR is performed. Can also be performed continuously.
- the amount of the PCR primer for the first step needs to be smaller than the amount of the PCR primer for the second step, and is preferably 100 times or less.
- the expression level of human WT1 mRNA can be easily measured by a one-step reaction in the same container, and as shown in Example 2, RT-PCR of the target gene. It can be detected with higher sensitivity than the two-step RT-PCR in which the reaction and the RT-PCR reaction of the housekeeping gene are performed separately. In other words, according to the method of the present invention, even a sample with a low concentration of human WT1 mRNA can be detected with high accuracy.
- This method can be carried out more easily by using a real-time PCR kit described below.
- the RT-PCR reagent kit of the present invention comprises a primer set for subjecting human WT1 mRNA to RT-PCR, a housekeeping gene, preferably GAPDH It includes both primer sets for subjecting mRNA to RT-PCR.
- the kit can include a probe used for detecting the amplification product of human WT1 mRNA and the amplification product of the housekeeping gene amplified by the RT-PCR method.
- kits from “(A1) Forward primer (SEQ ID NO: 3)” and “(A2) Reverse primer (SEQ ID NO: 4)” shown in Table 1 as a primer set for subjecting human WT1 mRNA to RT-PCR.
- (A3) Probe (SEQ ID NO: 5) As a sequence-specific binding probe used for detecting the primer set A and the human WT1 gene amplified product amplified with these primer sets, “(A3) Probe (SEQ ID NO: 5)” shown in Table 1 is included.
- the probe is preferably labeled in order to facilitate detection of the amplified product.
- the probe labeling method includes an RI method and a non-RI method, but it is preferable to use a non-RI method.
- Non-RI methods include a fluorescent labeling method, a biotin labeling method, a chemiluminescence method, and the like, and the fluorescent labeling method is preferably used.
- the fluorescent substance is not particularly limited as long as it can bind to the base moiety of nucleic acid, but cyanine dyes (Cy ⁇ DyeTM series Cy3 and Cy5 etc.), rhodamine 6G reagent, N-acetoxy-N2-acetylaminofluorene and its iodine Derivatives can be used.
- kits “(B1) Forward primer (SEQ ID NO: 9)” and “(B2) Reverse primer (SEQ ID NO: 10) shown in Table 2 as primer sets for subjecting human WT1 mRNA to the RT-PCR method.
- primer set B consisting of "Reverse primer (SEQ ID NO: 12)" and human GAPDH gene amplification products amplified with these primer sets Shown in Table 2 as a sequence-specific binding probes use may be mentioned those containing "(b3) Probe (SEQ ID NO: 8).”
- the RT-PCR kit of the present invention has various components (dNTP, Mg salt, buffer components for pH adjustment, etc.) necessary for the two reactions of reverse transcription and PCR, and reverse transcription activity. Enzymes can be included. Furthermore, the thing which added the component which stabilizes an enzyme, a ribonuclease inhibitor, etc. may be used.
- the RT-PCR kit of the present invention is a kit capable of quantifying the expression level of human WT1 mRNA in a simple, rapid and without cross-contamination problem according to the above method.
- kits examples include a kit containing various reagents used in the above-described method, a kit containing the reaction solution used in the present invention, and a kit containing a reaction container into which one batch of the reaction solution has been dispensed. Etc.
- the kit is particularly useful as a kit for various tests, particularly clinical diagnosis, and can be widely used for leukemia tests, solid cancer micrometastasis tests, residual microlesion tests, infectious disease tests, and the like.
- Example 1 One step and multiplex RT-PCR measurement (1) Primer and probe design Human WT1 mRNA is selected as the target gene to be measured, and GAPDH mRNA is selected as the endogenous control gene (correction gene) that corrects the expression level of the measurement target. Primer sets and probes that enable amplification and detection were designed and synthesized.
- the fluorescently labeled probe is labeled with FAM (6-carboxyfluorescein) at the 5 'end of the probe for detecting the target gene.
- FAM 6-carboxyfluorescein
- the 5 ′ end of the probe for detecting the correction gene was labeled with HEX (6-hexachlorofluorescein).
- HEX 6-hexachlorofluorescein
- ATTO-540Q ATTO-540Q
- Table 3 shows the primer and probe sequences used in this example.
- the sequence behind the portion where the WT1 mRNA sequence and GAPDH mRNA sequence were inserted was cleaved with the restriction enzyme EcoRI to obtain linear DNA.
- the T7 promoter sequence contained in the plasmid DNA was recognized, and T7 RNA polymerase, which is an enzyme that synthesizes RNA using the DNA as a template, was used to synthesize RNA sequences of WT1 mRNA and GAPDH mRNA.
- the synthesized RNA was diluted with TE buffer containing 50 ng / ⁇ L of E. coli transfer RNA, and RNA standards for the respective genes (WT1 and GAPDH) were prepared.
- the concentration of the WT1 RNA standard prepared in this way is 2.5 ⁇ 10 1 , 2.5 ⁇ 10 2 , 2.5 ⁇ 10 3 , 2.5 ⁇ 10 4 , 2.5 ⁇ 10 5 copies / test, and the concentration of the GAPDH RNA standard is 1.0 ⁇ 10 4 , 1.0 ⁇ 10 5 , 1.0 ⁇ 10 6 , 1.0 ⁇ 10 7 , 1.0 ⁇ 10 8 copies / test were adjusted.
- RT-PCR reaction was carried out by a one-step RT-PCR method in which reverse transcription reaction and PCR reaction were continuously performed in one tube.
- Reverse transcriptase Z05 DNA polymerase (Thermostable enzyme from Thermus species Z05: Roche Diagnostics) was used.
- (3-2) Reaction conditions (A) Reverse transcription reaction and PCR reaction After 5 minutes at 55 ° C, 5 minutes at 60 ° C, and 5 minutes at 65 ° C, the reverse transcription reaction was performed for 15 minutes, followed by heat denaturation at 92 ° C for 15 seconds, 60 PCR reaction consisting of annealing at 40 ° C. for 40 seconds and DNA extension reaction was repeated 45 cycles.
- (B) Reagent concentration The volume of the reaction solution was 20 ⁇ L, and the Primer concentration was 0.2 ⁇ M final concentration for each of the forward primer and reverse primer. The probe concentration was 0.1 ⁇ M final concentration.
- Fig. 1 (a) WT1 mRNA amplification curve when WT1 mRNA is amplified alone with various concentrations of WT1 RNA, and Fig. 2 (b) GAPDH mRNA alone with various concentrations of GAPDH mRNA amplified. GAPDH mRNA amplification curve when performed, Fig. 3 (c) WT1 mRNA amplification curve when WT1 mRNA and GAPDH ⁇ mRNA were simultaneously amplified with various concentrations of WT1 ⁇ RNA, and Fig. 4 (d) various concentrations The GAPDH-mRNA amplification curves when the GAPDH-RNA standard product was simultaneously amplified with WT1 mRNA and GAPDH mRNA were shown.
- Table 4 shows the number of cycles of amplification of WT1 mRNA when WT1 mRNA is amplified alone and WT1 mRNA and GAPDH mRNA are simultaneously amplified for various concentrations of WT1 RNA standard products.
- Table 5 shows the number of GAPDH-mRNA amplification cycles when GAPDH-mRNA was amplified alone and GWTDH-mRNA was simultaneously amplified for various concentrations of GAPDH-mRNA standard products.
- FIG. 1 shows a WT1 mRNA amplification curve when WT1 mRNA is amplified alone.
- WT1 mRNA when WT1 mRNA was amplified alone, it was possible to detect WT1 mRNA from 2.5 ⁇ 10 5 to 2.5 ⁇ 10 1 copies / test.
- WT1 mRNA and GAPDH mRNA were amplified simultaneously, it was possible to detect WT1 mRNA from 2.5 ⁇ 10 5 to 2.5 ⁇ 10 1 copies / test, as shown in FIG.
- the number of amplification cycles when WT1WT mRNA was amplified alone (amplification cycle numbers 18.63 to 32.09), and the number of amplification cycles when WT1 mRNA and GAPDH mRNA were simultaneously amplified (amplification cycle number 18.67).
- the difference from ⁇ 31.94) was as small as -0.15 to 0.06, and there was no significant difference in the number of amplification cycles between single amplification and simultaneous amplification. Therefore, even when the target gene WT1 mRNA and the correction gene are amplified simultaneously, the WT1 mRNA is amplified at the same number of amplification cycles as in the case of amplifying the target gene (WT1) mRNA) alone. It was considered possible to detect.
- the GAPDH mRNA amplification curve when GAPDH mRNA is amplified alone is shown in FIG. As shown here, when GAPDH mRNA was amplified alone, it was possible to detect GAPDH mRNA from 1.0 ⁇ 10 8 to 1.0 ⁇ 10 4 copies / test.
- Example 2 Dilution test using K562 extracted RNA
- a one-step and multiplex RT-PCR method for simultaneously amplifying WT1 mRNA and GAPDH mRNA, reverse transcription reaction and PCR in separate containers. Each was performed, and the measurement sensitivity was compared by a two-step RT-PCR method in which WT1 mRNA and GAPDH mRNA were separately amplified.
- the two-step RT-PCR method was performed using a WT1 mRNA measurement kit “Otsuka” (Otsuka Pharmaceutical Co., Ltd.).
- Primer and probe sequences Table 6 shows the sequences of primers and probes used for WT1 mRNA measurement and GAPDH mRNA measurement by one-step RT-PCR.
- the WT1 mRNA measurement kit “Otsuka” was used, so the primers and probe are unknown.
- RNA standard products prepared by the same method as described in Example 1 were used in the one-step RT-PCR method.
- WT1 RNA standard concentration is 2.5 ⁇ 10 1 , 2.5 ⁇ 10 3 , 2.5 ⁇ 10 5 , 2.5 ⁇ 10 7 copies / test
- GAPDH RNA standard concentration is 1.0 ⁇ 10 3 , 1.0 ⁇ 10 5 , 1.0 ⁇ 10 7 and 1.0 ⁇ 10 9 copies / test.
- a standard product provided in the WT1 mRNA measurement kit “Otsuka” was used.
- Test sample RNA extracted from WT1-positive leukemia cell line K562 was used as a test sample. Specifically, Total RNA extracted from K562 was used with TE buffer to which E. coli transfer RNA was added in advance to a final concentration of 50 ng / ⁇ L as carrier RNA in order to prevent nonspecific nucleic acid adsorption to the tube. The test sample was diluted to a final concentration of 2, 5 and 10 pg / ⁇ L.
- RT-PCR reaction One-step RT-PCR reaction was performed in the same manner as in Example 1. Two-step RT-PCR was performed using a WT1 mRNA measurement kit “Otsuka” (Otsuka Pharmaceutical Co., Ltd.) according to the package insert. Measurement was performed by double measurement for each test sample. The measurement results were calculated as copy / ⁇ g RNA, which is the number of WT1 mRNA per 1 ⁇ g of total RNA, according to the package insert of the WT1 mRNA measurement kit “Otsuka”.
- Results of dilution measurement using K562 extracted RNA Table 7 shows the results of dilution tests conducted using the 1-step RT-PCR method and 2-step RT-PCR method using K562 extracted RNA as the test sample. Show.
- K562-diluted RNA could be measured even after diluting until the RNA concentration reached 2.5 ⁇ pg / ⁇ L
- the two-step RT-PCR method When the K562-diluted RNA is diluted to an RNA concentration of 2.5 pg / ⁇ L, no amplified signal is detected by PCR, and even at 5 pg / ⁇ L, the double measurement data deviates from 17.2 and 1.9 copy / ⁇ gRNA, The measurable range as an effective value was considered to be up to 10 pg / ⁇ L. From these results, it was found that the one-step RT-PCR method has better measurement sensitivity than the two-step RT-PCR method.
- Example 3 Cross-reactivity test
- 1-step RT-PCR that simultaneously amplifies WT1 mRNA and GAPDH mRNA was used as a primer and a probe as shown in Table 8 (sequence set B) and in Table 9. Each set shown was performed and cross-reactivity was evaluated.
- HumanHGenome DNA (Merck KGaA, Darmstadt, German, Cat No. 69237) 250 ng, 50 ng, and 10 ng, and Total RNA 250ng extracted from WT1-positive leukemia cell line K562 (WT1 K562) were used. .
- the one-step RT-PCR reaction was performed in the same manner as in Example 1. Furthermore, amplification products obtained by PCR of Human Genome DNA and WT1 K562 mRNA were subjected to agarose gel electrophoresis under the following conditions to confirm the amplification products. The method of agarose electrophoresis followed a conventional method.
- Electrophoretic conditions 15 min, 4% E-gal, Photo condition: filter for SYBR, Photo directly from E-gal device, Shutter speed: 1/15, Squeeze: 4.5 Apply condition: Sample 2.5 ⁇ L + dH 2 O 16.5 ⁇ L Marker 2.5 ⁇ L + dH 2 O 16.5 ⁇ L [result] It is known that GAPDH pseudogene exists in Human Genomic DNA, although GAPDH gene does not exist. In this example, when one-step RT-PCR was performed using the primers and probe sequences shown in Table 8, as shown in lanes 1 to 3 of FIG. 5 (A), GAPDH was electrophoresed on Human Genome DNA. No matching band was found.
- GAPDH and GAPDH pseudogenes could be clearly distinguished, and it was confirmed that GAPDH pseudogenes were not misidentified as GAPDH.
- one-step RT-PCR was performed using the primers and probe sequences shown in Table 9, a band consistent with GAPDH was observed by electrophoresis as shown in lanes 1 to 3 of FIG. 5 (B). . That is, GAPDH and GAPDH pseudogenes could not be distinguished by one-step RT-PCR using the primers and probes.
- the base sequences shown in SEQ ID NOs: 3 to 12 mean the primers and probes described in Table 3. The correspondence is as detailed in Table 3.
- the base sequence shown in SEQ ID NO: 13 means the base sequence of the primers described in Table 9. This base sequence corresponds to the base sequence of region 56 to 74 of the human GAPDH gene (NM — 002046.3: SEQ ID NO: 2).
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Abstract
Description
(I-1)ヒトWT1 mRNAの発現量を1ステップRT-PCR法を用いて定量する方法であって、ヒトWT1 mRNAおよびハウスキーピング遺伝子(mRNA)の逆転写反応および伸長反応を、同時かつ、同一容器内で連続して進行させることを特徴とする、ヒトWT1 mRNAの発現量の定量方法。
(I-2)ハウスキーピング遺伝子がGAPDH mRNAである(I-1)に記載する方法。
(I-3)ヒトWT1 mRNAのPCR増幅に、
(a)配列番号3に示す塩基配列からなるフォーワードPCRプライマーと配列番号4に示す塩基配列からなるリバースPCRプライマーとからなるプライマーセット、または
(b)配列番号9に示す塩基配列からなるフォーワードPCRプライマーと配列番号10に示す塩基配列からなるリバースPCRプライマーとからなるプライマーセット
を用いる(I-1)または(I-2)に記載する方法。
(I-4)ヒトWT1 mRNAのPCR増幅に、
(a’)配列番号3に示す塩基配列からなるフォーワードPCRプライマーと配列番号4に示す塩基配列からなるリバースPCRプライマーとからなるプライマーセット、及び標識された配列番号5に示す塩基配列からなるプローブ、または
(b’)配列番号9に示す塩基配列からなるフォーワードPCRプライマーと配列番号10に示す塩基配列からなるリバースPCRプライマーとからなるプライマーセット、及び標識された配列番号11に示す塩基配列からなるプローブ
を用いる(I-1)または(I-2)に記載する方法。
(I-5)ヒトWT1 mRNAのPCR増幅に、さらに
(c)配列番号6に示す塩基配列からなるフォーワードPCRプライマーと配列番号7若しくは12に示す塩基配列からなるリバースPCRプライマーとからなるプライマーセット
を用いる(I-3)または(I-4)に記載する方法。
(I-6)ヒトWT1 mRNAのPCR増幅に、さらに
(c’)配列番号6に示す塩基配列からなるフォーワードPCRプライマーと配列番号7若しくは12に示す塩基配列からなるリバースPCRプライマーとからなるプライマーセット、及び標識された配列番号8に示す塩基配列からなるプローブ
を用いる(I-3)または(I-4)に記載する方法。
(II-1)(a)配列番号3に示す塩基配列からなるフォーワードPCRプライマーと配列番号4 に示す塩基配列からなるリバースPCRプライマーとからなるプライマーセット、または
(b)配列番号9に示す塩基配列からなるフォーワードPCRプライマーと配列番号10に示す塩基配列からなるリバースPCRプライマーとからなるプライマーセット、
を含むヒトWT1 mRNAの発現量を定量するためのリアルタイムPCR用キット。
(II-2)(a’)配列番号3に示す塩基配列からなるフォーワードPCRプライマーと配列番号4に示す塩基配列からなるリバースPCRプライマーとからなるプライマーセット、及び標識された配列番号5に示す塩基配列からなるプローブ、または
(b’)配列番号9に示す塩基配列からなるフォーワードPCRプライマーと配列番号10に示す塩基配列からなるリバースPCRプライマーとからなるプライマーセット、及び標識された配列番号11に示す塩基配列からなるプローブ、
を含むヒトWT1 mRNAの発現量を定量するためのリアルタイムPCR用キット。
(II-3)さらに(c)配列番号6に示す塩基配列からなるフォーワードPCRプライマーと配列番号7若しくは12に示す塩基配列からなるリバースPCRプライマーとからなるプライマーセットを含む、
(II-1)または(II-2)に記載するヒトWT1 mRNAの発現量を定量するためのリアルタイムPCR用キット。
(II-4)さらに(c’)配列番号6に示す塩基配列からなるフォーワードPCRプライマーと配列番号7若しくは12に示す塩基配列からなるリバースPCRプライマーとからなるプライマーセット、及び標識された配列番号8に示す塩基配列からなるプローブ
を用いる、(II-1)または(II-2)に記載するヒトWT1 mRNAの発現量を定量するためのリアルタイムPCR用キット。
本発明の方法は、ヒトWT1 mRNAの発現量を1ステップRT-PCR法を用いて定量する方法である。
本発明のRT-PCR用試薬キットは、ヒトWT1 mRNAをRT-PCR法に供するためのプライマーセットと、ハウスキーピング遺伝子、好ましくはGAPDH mRNAをRT-PCR法に供するためのプライマーセットの両方を包含することを特徴とする。また当該キットには、RT-PCR法で増幅されたヒトWT1 mRNAの増幅産物、及びハウスキーピング遺伝子の増幅産物を検出するために使用されるプローブを含めることができる。
(1)プライマーとプローブの設計
測定対象の目的遺伝子としてヒトWT1 mRNA,測定対象の発現量を補正する内在性コントロール遺伝子(補正用遺伝子)としてGAPDH mRNAを選択し、それぞれの遺伝子に対して特異的増幅と検出を可能とするプライマーセット及びプローブを設計し、合成した。
標準品は、WT1 mRNAおよびGAPDH mRNAを発現している白血病細胞株K562よりRNAを抽出し、このRNAを鋳型として、 WT1 mRNAおよびGAPDH mRNAの塩基配列にそれぞれ相補的なプライマーを用いて、RT-PCRを行い、WT1 mRNAおよびGAPDH mRNAの一部の塩基配列を得た。得られたWT1 mRNA配列およびGAPDH mRNA配列をpT7blueプラスミドベクターにクローニングし、大腸菌DH5α株を形質転換した。次いでこの形質転換大腸菌を培養し、プラスミドDNAを抽出した。プラスミドDNA中、WT1 mRNA配列およびGAPDH mRNA配列が挿入されている部分より後ろにある配列を、制限酵素EcoRIを用いて切断し、直鎖状のDNAとした。プラスミドDNAに含まれるT7プロモーター配列を認識し、DNAを鋳型としてRNAを合成する酵素であるT7 RNAポリメラーゼを用いて、WT1 mRNA及びGAPDH mRNAのRNA配列を合成した。合成したRNAを、反応容器への非特異的な吸着を防ぐために50 ng/μLの大腸菌トランスファーRNAを含むTE バッファーで希釈し、それぞれの遺伝子(WT1およびGAPDH)のRNA標準品を調製した。
RT-PCR反応は、逆転写反応とPCR反応を一つのチューブ内で連続して行う1ステップRT-PCR法を行った。
Z05 DNA polymerase(Thermostable enzyme from Thermus species Z05:Roche Diagnostics社)を使用した。
(a)逆転写反応とPCR反応
55℃で5分間、60℃で5分間、65℃で5分間の計15分間かけて逆転写反応を行った後、92℃で15秒間の熱変性、60℃で40秒間のアニーリング、及びDNA伸長反応からなるPCR反応を45サイクロ繰り返した。
反応液の容量を20μLとし、その中のPrimer濃度は、Forward primer、及びReverse primerそれぞれ終濃度を0.2μMとした。Probe濃度は終濃度を0.1μMとした。
RT-PCR法は、Applied Biosystems 7500 Fast Realtime PCR system(ライフテクノロジーズ社)を用いて行った。
(4-1)蛍光増幅曲線の確認
(a)WT1 RNA標準品をWT1 mRNAを単独で増幅を行った場合、(b)GAPDH RNA標準品をGAPDH mRNAを単独で増幅を行った場合、及び(c)WT1 RNA標準品及びGAPDH RNA標準品のそれぞれについてWT1 mRNA及びGAPDH mRNAを同時に増幅を行った場合の、蛍光増幅曲線と増幅サイクル数を確認した。
本実施例では、WT1 mRNAとGAPDH mRNAを同時に増幅する、1ステップかつマルチプレックスなRT-PCR法と、逆転写反応とPCRを別の容器でそれぞれ行い、WT1 mRNAとGAPDH mRNAを別個に増幅する2ステップRT-PCR法とで、測定感度を比較した。なお、2ステップRT-PCR法は、WT1 mRNA測定キット「オーツカ」(大塚製薬株式会社)を使用して行った。
1ステップRT-PCR法によるWT1 mRNA測定及びGAPDH mRNA測定に使用したプライマー及びプローブの配列を表6に示す。なお2ステップ RT-PCR法は、WT1 mRNA測定キット「オーツカ」を使用したため、プライマー及びプローブは不明である。
標準品(WT1 mRNA、GAPDH mRNA)として、1ステップ RT-PCR法では、実施例1に記載した方法と同様の方法で調製したRNA標準品を用いた。WT1 RNA標準品の濃度を2.5×101,2.5×103,2.5×105,2.5×107copies/test,GAPDH RNA標準品の濃度を1.0×103,1.0×105,1.0×107,1.0×109copies/testとした。2ステップ RT-PCR法では、WT1 mRNA測定キット「オーツカ」に備え付けられた標準品を使用した。
被験試料として、WT1陽性白血病細胞株K562より抽出したRNAを用いた。具体的には、K562より抽出したTotal RNAを、チューブへの非特異的な核酸の吸着を防ぐためにキャリアRNAとして大腸菌トランスファーRNAを終濃度50ng/μLとなるようにあらかじめ添加したTE bufferを用いて、最終濃度が2、5、10 pg/μLになるように希釈して、これを被験試料とした。
1ステップRT-PCR反応は、実施例1と同様の方法で行った。2ステップRT-PCRは、WT1 mRNA測定キット「オーツカ」(大塚製薬株式会社)を用いてその添付文書に従って行った。測定は各被験試料について2重測定で行った。測定結果はWT1 mRNA測定キット「オーツカ」の添付文書に従い、Total RNA 1μg当たりのWT1 mRNA数であるcopy/μgRNAとして算出した。
(5-1)K562抽出RNAによる希釈測定結果
表7にK562抽出RNAを被験試料として、1ステップRT-PCR法及び2ステップRT-PCR法を用いて実施した希釈試験の結果を示す。
本実施例では、WT1 mRNAとGAPDH mRNAを同時に増幅する1ステップRT-PCRを、プライマーおよびプローブとして、表8に示すセット(配列セットB)、及び表9に示すセットをそれぞれ用いて実施し、交差反応性を評価した。
<アガロースゲル電気泳動条件>
泳動条件:15min、4%E-gal、
Photo条件:SYBR用filter、
E-gal装置より直接photo、
シャッタースピード:1/15、
しぼり:4.5
Apply条件:Sample 2.5μL+dH2O 16.5μL
Marker 2.5μL+dH2O 16.5μL
[結果]
Human Genomic DNAにはGAPDHの遺伝子は存在しないものの、GAPDHの偽遺伝子が存在することが知られている。本実施例では、表8に示したプライマーおよびプローブ配列を用いて1ステップRT-PCRを実施すると、図5(A)のレーン1~3に示すように、Human Genome DNAにおいて電気泳動でGAPDHと一致するバンドは認められなかった。すなわち、本発明のプライマーおよびプローブを用いた1ステップRT-PCRによれば、GAPDHとGAPDHの偽遺伝子とが明確に識別でき、GAPDHの偽遺伝子をGAPDHと誤認することがないことが確認できた。一方、表9に示したプライマーおよびプローブ配列を用いて1ステップRT-PCRを実施すると、図5(B)のレーン1~3に示すように、電気泳動でGAPDHと一致するバンドが認められた。すなわち、当該プライマーおよびプローブを用いた1ステップRT-PCRではGAPDHとGAPDHの偽遺伝子とを区別することができなかった。
Claims (10)
- 被験試料におけるヒトWT1 mRNAの発現量を1ステップRT-PCR法を用いて定量する方法であって、
ヒトWT1 mRNAおよびハウスキーピング遺伝子(mRNA)の逆転写反応および伸長反応を、当該被験試料において同時かつ同一容器内で連続して進行させることを特徴とする、ヒトWT1 mRNAの発現量の定量方法。 - ハウスキーピング遺伝子がGAPDH mRNAである請求項1に記載する方法。
- ヒトWT1 mRNAのPCR増幅に、
(a)配列番号3に示す塩基配列からなるフォーワードPCRプライマーと配列番号4 に示す塩基配列からなるリバースPCRプライマーとからなるプライマーセット、または
(b)配列番号9に示す塩基配列からなるフォーワードPCRプライマーと配列番号10に示す塩基配列からなるリバースPCRプライマーとからなるプライマーセットを用いる請求項1または2に記載の方法。 - ヒトWT1 mRNAのPCR増幅に、
(a’)配列番号3に示す塩基配列からなるフォーワードPCRプライマーと配列番号4に示す塩基配列からなるリバースPCRプライマーとからなるプライマーセット、及び標識された配列番号5に示す塩基配列からなるプローブ、または
(b’)配列番号9に示す塩基配列からなるフォーワードPCRプライマーと配列番号10に示す塩基配列からなるリバースPCRプライマーとからなるプライマーセット、及び標識された配列番号11に示す塩基配列からなるプローブ
を用いる、請求項1または2に記載する方法。 - ヒトWT1 mRNAのPCR増幅に、さらに
(c)配列番号6に示す塩基配列からなるフォーワードPCRプライマーと配列番号7若しくは12に示す塩基配列からなるリバースPCRプライマーとからなるプライマーセット
を用いる、請求項3または4に記載する方法。 - ヒトWT1 mRNAのPCR増幅に、さらに
(c’)配列番号6に示す塩基配列からなるフォーワードPCRプライマーと配列番号7若しくは12に示す塩基配列からなるリバースPCRプライマーとからなるプライマーセット、及び標識された配列番号8に示す塩基配列からなるプローブ
を用いる、請求項3または4に記載する方法。 - (a)配列番号3に示す塩基配列からなるフォーワードPCRプライマーと配列番号4 に示す塩基配列からなるリバースPCRプライマーとからなるプライマーセット、または
(b)配列番号9に示す塩基配列からなるフォーワードPCRプライマーと配列番号10に示す塩基配列からなるリバースPCRプライマーとからなるプライマーセット、
を含むヒトWT1 mRNAの発現量を定量するためのリアルタイムPCR用キット。 - (a’)配列番号3に示す塩基配列からなるフォーワードPCRプライマーと配列番号4に示す塩基配列からなるリバースPCRプライマーとからなるプライマーセット、及び標識された配列番号5に示す塩基配列からなるプローブ、または
(b’)配列番号9に示す塩基配列からなるフォーワードPCRプライマーと配列番号10に示す塩基配列からなるリバースPCRプライマーとからなるプライマーセット、及び標識された配列番号11に示す塩基配列からなるプローブ、
を含むヒトWT1 mRNAの発現量を定量するためのリアルタイムPCR用キット。 - さらに(c)配列番号6に示す塩基配列からなるフォーワードPCRプライマーと配列番号7若しくは12に示す塩基配列からなるリバースPCRプライマーとからなるプライマーセットを含む、
請求項7または8に記載するヒトWT1 mRNAの発現量を定量するためのリアルタイムPCR用キット。 - さらに(c’)配列番号6に示す塩基配列からなるフォーワードPCRプライマーと配列番号7若しくは12に示す塩基配列からなるリバースPCRプライマーとからなるプライマーセット、及び標識された配列番号8に示す塩基配列からなるプローブ
を用いる、請求項7または8に記載するヒトWT1 mRNAの発現量を定量するためのリアルタイムPCR用キット。
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CN111500519B (zh) * | 2020-03-14 | 2022-03-08 | 哈尔滨工业大学(深圳)(哈尔滨工业大学深圳科技创新研究院) | 一种触发及强化节杆菌产生胞外超氧自由基的方法 |
WO2023147445A2 (en) * | 2022-01-27 | 2023-08-03 | Oregon Health & Science University | Cell-free rna biomarkers for the detection of cancer or predisposition to cancer |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH1189596A (ja) | 1997-09-19 | 1999-04-06 | Takara Shuzo Co Ltd | Rna量の測定方法並びに測定キット |
JPH1189599A (ja) | 1997-09-24 | 1999-04-06 | Haruo Sugiyama | 補正競合rt−pcr法によるヒトwt1発現定量法 |
JP2002136300A (ja) * | 2000-08-25 | 2002-05-14 | Otsuka Pharmaceut Co Ltd | 白血病キメラ遺伝子の検出方法 |
JP2006223303A (ja) * | 2005-01-21 | 2006-08-31 | Canon Inc | 微量胃癌細胞の検出法 |
JP2009509502A (ja) * | 2005-09-19 | 2009-03-12 | ベリデックス・エルエルシー | 原発不明がんの原発巣を同定するための方法および材料 |
JP2012525825A (ja) * | 2009-05-06 | 2012-10-25 | サノフイ | 可逆的に不死化された細胞及びそれに関連する方法 |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8535914B2 (en) | 2005-01-21 | 2013-09-17 | Canon Kabushiki Kaisha | Probe, probe set and information acquisition method using the same |
US20070031966A1 (en) | 2005-07-18 | 2007-02-08 | Regents Of The University Of Michigan | Renal progenitor cells from embryonic stem cells |
CN101182570A (zh) * | 2007-11-15 | 2008-05-21 | 南方医科大学 | 一种检测wt1和mdr1基因异常表达的多重定量pcr试剂盒 |
CN101760522A (zh) * | 2008-10-23 | 2010-06-30 | 上海复星医药(集团)股份有限公司 | 一种使用gapdh基因分析arhgdib基因表达量的rt-pcr技术 |
CN101781677A (zh) * | 2009-01-15 | 2010-07-21 | 中山大学达安基因股份有限公司 | 检测白血病广谱标记物WT1基因mRNA表达的试剂盒 |
US8426133B2 (en) * | 2009-05-26 | 2013-04-23 | Quest Diagnostics Investments Incorporated | Methods for detecting gene dysregulation by intragenic differential expression |
CN102443581A (zh) * | 2010-10-09 | 2012-05-09 | 清华大学 | 用于检测p53基因表达的引物对及其应用 |
CN102534045A (zh) * | 2010-12-30 | 2012-07-04 | 上海复星医学科技发展有限公司 | 一种丙型肝炎病毒基因分型荧光pcr检测试剂盒 |
-
2014
- 2014-01-22 US US14/762,454 patent/US10280467B2/en active Active
- 2014-01-22 KR KR1020187010959A patent/KR20180043401A/ko active IP Right Grant
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Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH1189596A (ja) | 1997-09-19 | 1999-04-06 | Takara Shuzo Co Ltd | Rna量の測定方法並びに測定キット |
JPH1189599A (ja) | 1997-09-24 | 1999-04-06 | Haruo Sugiyama | 補正競合rt−pcr法によるヒトwt1発現定量法 |
JP2002136300A (ja) * | 2000-08-25 | 2002-05-14 | Otsuka Pharmaceut Co Ltd | 白血病キメラ遺伝子の検出方法 |
JP2006223303A (ja) * | 2005-01-21 | 2006-08-31 | Canon Inc | 微量胃癌細胞の検出法 |
JP2009509502A (ja) * | 2005-09-19 | 2009-03-12 | ベリデックス・エルエルシー | 原発不明がんの原発巣を同定するための方法および材料 |
JP2012525825A (ja) * | 2009-05-06 | 2012-10-25 | サノフイ | 可逆的に不死化された細胞及びそれに関連する方法 |
Non-Patent Citations (13)
Title |
---|
BLOOD, vol. 82, 1993, pages 1929 - 1936 |
BLOOD, vol. 88, 1996, pages 2267 - 2278 |
BLOOD, vol. 88, 1996, pages 4396 - 4398 |
BLOOD, vol. 90, 1997, pages 1217 - 1225 |
CALL, K. M. ET AL., CELL, vol. 60, 1990, pages 509 - 520 |
CLIN. CHEM., vol. 41, 1995, pages 819 - 825 |
INOUE, K. ET AL., BLOOD, vol. 84, no. 9, 1994, pages 3071 - 3079 |
JPN. J. CANCER RES., vol. 90, 1999, pages 194 - 204 |
MIWA, H. ET AL., LEUKEMIA, vol. 6, 1992, pages 405 - 409 |
NIRDE ET AL., J. STEROID BIOCHEM. MOLEC. BIOL., vol. 66, no. 1-2, 1998, pages 35 - 43, XP055266556 * |
PROC. NATL. ACAD. SCI. USA, vol. 87, 1990, pages 2725 - 2729 |
SASAKI: "Bessatsu Mokutekibetsu de Eraberu PCR Jikken Protocol Shippai shinai Tameno Jikken Sosa to Joken Settei no Kotsu", EXPERIMENTAL MEDICINE, vol. 201, 1 January 2011 (2011-01-01), pages 45 - 46, XP008181711 * |
See also references of EP2949760A4 |
Cited By (8)
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CN104328209A (zh) * | 2014-11-24 | 2015-02-04 | 济南市中心医院 | 白血病微小残留病wt1基因快速检测方法的引物和试剂盒 |
CN104328209B (zh) * | 2014-11-24 | 2016-06-15 | 济南市中心医院 | 白血病微小残留病wt1基因快速检测方法的引物和试剂盒 |
WO2018016474A1 (ja) | 2016-07-19 | 2018-01-25 | 大塚製薬株式会社 | 小児急性リンパ性白血病の血液学的病期の判定補助方法 |
JPWO2018016474A1 (ja) * | 2016-07-19 | 2019-05-09 | 大塚製薬株式会社 | 小児急性リンパ性白血病の血液学的病期の判定補助方法 |
JP7002450B2 (ja) | 2016-07-19 | 2022-02-04 | 大塚製薬株式会社 | 小児急性リンパ性白血病の血液学的病期の判定補助方法 |
JP2018068140A (ja) * | 2016-10-25 | 2018-05-10 | アークレイ株式会社 | Abl遺伝子増幅用プライマー、核酸増幅方法及び核酸増幅用キット |
JP7007796B2 (ja) | 2016-10-25 | 2022-02-10 | アークレイ株式会社 | Abl遺伝子増幅用プライマー、核酸増幅方法及び核酸増幅用キット |
JP7496094B2 (ja) | 2019-02-28 | 2024-06-06 | 住友ファーマ株式会社 | がんを治療又は予防するための医薬組成物の効果を期待できる対象を選択する方法 |
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JPWO2014115779A1 (ja) | 2017-01-26 |
AU2014208593A2 (en) | 2015-11-12 |
KR20150109427A (ko) | 2015-10-01 |
AU2014208593A1 (en) | 2015-07-30 |
US10280467B2 (en) | 2019-05-07 |
EP2949760A4 (en) | 2016-08-24 |
CA2898965A1 (en) | 2014-07-31 |
KR20180043401A (ko) | 2018-04-27 |
CN104937112A (zh) | 2015-09-23 |
CN104937112B (zh) | 2018-04-24 |
JP6636247B2 (ja) | 2020-01-29 |
EP2949760B1 (en) | 2019-04-24 |
ES2731780T3 (es) | 2019-11-19 |
EP2949760A1 (en) | 2015-12-02 |
EP2949760A9 (en) | 2016-06-22 |
US20160333415A1 (en) | 2016-11-17 |
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