44 results about "CDKN2A" patented technology

The invention relates to tumor susceptibility 62 genes and application thereof. The tumor susceptibility 62 genes comprise PTEN, STK11, CDH1, TP53, BRCA1, BRCA2, PALB2, CHEK2, ATM, BRIP1, NBN, RAD51C, MLH1, MSH2, MSH6, PMS2, BARD1, RAD51D, MRE11A, MUTYH, PMS1, RAD50, XRCC2, AKT1, PIK3CA, FANCC, RECQL, CCND1, ERBB2, ESR1, GATA3, FGFR1, MAP2K4, MAP3K1, BAI3, CTNNB1, BRAF, KRAS, CTNNA1, EPCAM, APC, BLM, SMAD4, BMPR1A, POLD1, POLE, AXIN2, MEN1, KIT, EGFR, EZH2, PRF1, CDKN2A, CDK4, BAP1, RB1, ERCC2, VHL, MET, FH, FLCN and RET. The detection of the genes can be used for evaluating tumor susceptibility.

The present invention provides a diabetes type II gene susceptivity and pre-warning detection kit, which is characterized in that seven nucleic acid (DNA and RNA) molecule markers are combined, wherein the seven nucleic acid (DNA and RNA) molecule markers comprise APM1 (+45), CDKAL1 (rs10946398), TCF7L2 (rs7903146) , CDKN2A/2B (rs10811661), KCNQ1 (rs2237892), VDR (FokI) and SLC30A8 (rs13266634). The kit comprises: specific amplification primer pairs and DNA sequencing primer pairs of the gene polymorphism loci, PCR reaction liquids, PCR product enzymolysis liquids and DNA sequencing reaction liquids. According to the present invention, detection is performed by using the kit, gene information is processed and analyzed, diabetes type II susceptivity of a healthy subject is evaluated, and guiding significance is provided for personalized treatment and health care of diabetes type II people.

The present disclosure relates to a method of treating cancer using a composition comprising Nelfinavir, Metformin, Rosuvastatin, optionally along with a pharmaceutically acceptable excipient. The said composition is used for the treatment of cancer caused due to aberration in PTEN gene, optionally along with aberration in TP53 gene and related genes selected from group comprising PI3K, CDKN2A, MDM2 and MDM4.

The invention discloses gene markers for forecasting an immunotherapy effect on a cancer and application of the gene markers. The markers comprise BRD4, RPS6KA4, TET1, BCL10, FGFR2, RAD51C, TCF7L2, TGFBR1, AR, BBC3, H3C11, TSC2, NSD1, PNRC1, IGF2, H3C3, SOCS1, TCF3, TSHR, PMS2, EGFR and CDKN2A. According to the application, a model constructed by 22 genes can be used for predicting an immunotherapy effect and better instructing clinical medication, and the susceptibility and specificity of prediction of the model are superior to those of PD-L1 expression.

The invention relates to the technical field of molecular diagnosis, in particular to a composition for detecting mutation of lung adenocarcinoma cell cycle progress pathway related genes (CDKN2A, CCND1, CCNE1, CDK4 and RB1) and application of the composition, and the composition is composed of reagents for detecting the expression quantity of the related genes. RNA sequencing, LASSO and binary classification Logistic regression are applied to screen genes related to the cell cycle progress pathway, a score Score is constructed, a cut-off value corresponding to the Score in the lung adenocarcinoma is obtained through ROC analysis, and the method can be used for predicting mutation of the lung adenocarcinoma cell cycle progress pathway related genes. The specific gene mutation of the lung adenocarcinoma is predicted by using the expression quantity of the gene composition, and verification shows that the prediction method has the advantages of high accuracy and good specificity, and has a good application prospect.

The invention relates to the technical field of gene detection, and discloses a detection kit for oral squamous cell carcinoma lymph node metastasis prediction. The kit comprises forward primer and reverse primer sequences of 7 kinds of genes including PDGFRA, PLAU, SOX9, SPP1, CDKN2A, CASP1 and MAL. The invention also discloses a method for screening the gene or the gene combination for the oralsquamous cell carcinoma lymph node metastasis prediction. The detection kit can be used for objectively, accurately and sensitively predicting the oral squamous cell carcinoma lymph node metastasis condition, so that the survival rate of the oral squamous cell carcinoma patients can be favorably improved.

The present invention relates to a method for treating breast cancer in a subject having a breast cancer of the triple-negative type, which method comprises the step of administering to said subject a therapeutically effective amount of a modulator of the protein tyrosine phosphatase, non-receptor type 11 (PTPN11) gene or of its gene product (Shp2). The present invention also relates to a method for treating breast cancer in a subject having a breast cancer over-expressing the “SHP2 signature” genes, as compared to normal breast tissue samples, which method comprises the step of administering to said subject a therapeutically effective amount of a modulator of the protein tyrosine phosphatase, non-receptor type 11 (PTPN11) gene or of its gene product (Shp2), wherein said “SHP2 signature” genes consist of the genes SGCB, ZSCAN12, ID4, ZIC3, CPVL, HLA-A, MCOLN3, SPATA18, TMEM45A, GNAL, CYBRD1, TSPAN7, ZEB1, CNTLN, NEFL, CENPV, ARL6, HPRT1, LRRC34, PDPN, BEND7, SLC16A10, FAM27E1, PLEKHA1, HERC5, CHIC1, PHF6, ELOVL4, ANTXR1, PRAME, SCML1, CLIP4, CECR2, CNOT10, IGF2BP3, NAP1L3, GPC3, KIAA1804, DGKE, FAS, EPHA6, KDELC1, CRISPLD1, DOCK3, ACSL4, CNTNAP3, PLEKHM3, RDX, TBX18, RRAGD, HOXB5, SNCA, FUNDC2, ITGA8, HFM1, IGF2BP2, CCND2, SGTB, MKX, CRYBG3, WBP5, LPHN3, BEX4, CPNE8, GLDC, SLC35F1, HOXA13, SERPINF1, NEFM, SYCP2L, FHL1, APOBEC3C, CALD1, FKBP10, HOXD11, DENND2C, LRRC49, FAM55C, KIAA0408, HOXB9, C160RF62, ACN9, TUSC3, ELOVL2, SPOCK3, HOXB6, WDR35, MPP1, FBX038, PRKAA2, SLAIN1, NPHP3, KIAA1524, PRPS1, GJC1, AMOT, SLC9A6, KCTD12, NUP62CL, DZIP3, JAM3, HOXA9, ANKRD19, CDKN2A, BCAT1, OAT, LPHN2, CCDC82, HSD17B11, SAMHD1, WDR17, STK33, GSTP1, TRPC1, CKB, LIN28B, ALDH1L2, SACS, CLGN, MY03A, EPB41L3, SLC25A27, VCAN, GPX8, GALNT13, PVRL3, MOXD1, HEY1, MAP7D3, ESD, MPP6, EYA4, SPG20, ZDBF2, ZNF204, IFT57, AKR1B1, ADAT2, ZNF717, CCDC88A, ZNF215, MIDI, FBN2, LOC100130876, TCEAL8, IGF2BP1, ANKRD18B, PLAGL1, PM20D2, LDHB, C150RF51, PTPN11, EPB41L2, TLE4, GOLM1, C60RF192, HOXD13, SLIT2, UCHL1, DYNC2H1, CPS1, GPR180, PYGL, NRN1, PRTFDC1, SLC16A1, DSC3, TMC01, LRCH2, SLC6A15, DZIP1, HOXA5, HSPA4L, CDR1, PLS3, ECHDC1, SMARCA1, CXORF57, HOXD10, and IRS4.

The invention relates to the technical field of biological medicines, in particular to application of miR-663a or a target gene CKDN2A thereof in thin endometrium. The invention discloses application of a reagent for detecting the expression level of miR-663a or a target gene CKDN2A of the miR-663a in preparation of a product for detecting thin endometrium. Furthermore, the invention further discloses a biological agent for relieving or repairing the hypoxia injury EEC and application of the biological agent. According to the application, the miR-663 is screened out through a transcriptome sequencing technology, a cell function experiment and a Western blot experiment show that the miR-663 can obviously inhibit the occurrence of EEC hypoxia injury, the inhibition can be realized through a target gene CDKN2A, and a new thought is provided for the treatment of thin endometrium.

The present invention discloses a universal polypeptide vaccine. The universal polypeptide vaccine comprises at least one of the following 6 mutations: KRAS-G12R, KRAS-G12V, CDKN2A-H83Y, KRAS-Q61H, TP53-R248W and CDKN2A-P94L. Specifically, the universal polypeptide vaccine comprises at least one of the 6 mutations. The universal polypeptide vaccine can be used for preparing drugs for treating/preventing cancers (pancreatic cancers). The universal polypeptide vaccine has relatively good immunotherapeutic effects on the pancreatic cancers.

The invention discloses lung cancer targeted drug and chemotherapy drug genomes and an application thereof in lung cancer clinical drug treatment. The targeted drug genome comprises AKT1, ALK, BRAF, CCND1, CDKN2A, DDR2, EGFR, ERBB2, ERBB4, FBXW7, FGFR1, FGFR2, FGFR3, HRAS, IGF1R, KDR, KIT, KRAS, MAP2K1, MET, NF1, NRAS, NTRK1, NTRK3, PDGFRA, PIK3CA, PTEN, RET, ROS1, STK11 and TP53; and the chemotherapy drug genome comprises ABCB1, CDA, CEP72, CYP1B1, CYP2C8, DPYD, ERCC1, ERCC2, GSTM, GSTP1, MTHFR, RRM1, SLCO1B1, TEKT4, TPMT, TYMS, UMPS, XPC and XRCC1. The lung cancer targeted drug and chemotherapy drug genomes disclosed by the invention are applied to guidance of clinical precise chemotherapy of the lung cancer or auxiliary diagnosis of the lung cancer and curative effect and after-healingmonitoring, can provide the most effective drug selection for lung cancer patients with drug resistance or toxic and side effect intolerance caused by conventional drugs and targeted and chemotherapydrug requirements, improve the drug treatment effect, and reduce the toxic and side effects of the drugs.

The present application discloses a method to predict responsiveness of a patient, with cancer, to treatment with an MDM2 antagonist of formulae I, II and III as disclosed herein, said method comprising measuring m RNA expression levels of at least MDM2, preferably of a four gene panel comprising MDM2, XPC, BBC3 and CDKN2A, as a biomarker for predicting the response.

The invention provides a target genome for gene detection of a non-small cell lung cancer patient and a related evaluation method, application and kit. The target genome is used for evaluating whetherthe non-small cell lung cancer patient has the necessity of tumor mutation load detection or not, and the target genome comprises the following genes of EGFR, TP53, CDKN2A and SDHA.

The invention discloses a primer group, a kit and a method for detecting head and neck tumor gene survival correlation. The primer group at least comprises nucleotide sequences of two groups of primers, and a plurality of genes are preferably CDKN2A. When the CDKN2A high amplification condition is detected, patients can be recommended to accept CDKN2A inhibitor medicine treatment, so that the patients suitable for CDKN2A targeted treatment can benefit; if the CDKN2A high amplification does not exist, other treatment medicine needs to be considered in time; the condition that the patients suffer from the potential toxic effect of the medicine and unnecessary economic burden is avoided; the best treatment opportunity is missed; and good guidance effects are achieved.