Super-mutant type tumor molecule subtype gene and application thereof
A molecular typing and mutation technology, which can be used in the determination/inspection of microorganisms, biochemical equipment and methods, DNA/RNA fragments, etc. Prompt the response of immunotherapy and the possibility of final benefit, so as to achieve good benefits and good clinical guiding significance.
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Embodiment 1
[0030] Example 1 Preparation of Genomic DNA Samples and Determination of Tumor Somatic Mutation Sites
[0031] In order to detect the somatic mutation of colorectal cancer, the present invention completed the high-throughput sequencing of 338 colorectal cancer tissue samples in two stages, and completed the high-throughput sequencing of 80 cases of colorectal cancer in the first stage, of which 10 cases For whole genome sequencing, 70 cases for whole exome sequencing. Through the first stage of high-frequency gene analysis, further combining the high-frequency genes in the TCGA database and COSMIC database, and the NCCN guidelines for the diagnosis and treatment of hereditary colorectal cancer, the present invention designed a gene group comprising 524 genes (Table 1), Capture probes targeting this gene group were customized for the second stage of sequencing. In the second phase, the targeted sequencing of 258 colorectal cancer tissue samples was completed using the capture ...
Embodiment 2
[0034] Example 2 Establishment of a gene mutation prognosis prediction model for hypermutated colorectal cancer
[0035] Since the currently approved immunotherapy drugs are mainly aimed at tumor patients with dMMR and MSI‐H, the characteristics of these patients at the genomic level are mainly hypermutations. Tumors with a mutation burden greater than 10 Mut / Mb were defined as hypermutated tumors. Among the 338 cases of colorectal cancer (ZJU data set) in Example 1, 45 cases were determined to be hypermutated. In addition, in order to verify the stability and universality of the model, the present invention downloaded a total of 382 cases of colorectal cancer data from TGCA as independent verification data (TCGA data set), and according to the same standard, 63 cases were designated as hypermutated colorectal cancer. Further, the present invention requires patient data with a follow-up time of more than 24 months for the establishment of a prognostic model, so 45 cases from...
Embodiment 3
[0037] Example 3 Analysis of colorectal cancer from ZJU and TCGA datasets using DOCK2 gene prognostic prediction model
[0038] Since hypermutated and microsatellite unstable colorectal cancers account for about 15% of the total, the number of patients in a single data set is relatively small. In order to further fully demonstrate the beneficial effects of the present invention, the present invention will use the colorectal Integrate the cancer data set, apply the DOCK2 gene prognosis prediction model constructed in Example 2, analyze the hypermutated colorectal cancer in the integrated data set, and distinguish it as DOCK2 wild type according to the mutation status of the DOCK2 gene in each patient in Table 2 group and DOCK2 mutant group, see figure 1 , compared with patients in the DOCK2 wild-type group, the hazard ratio of the DOCK2 mutant group was 1.54 (95% confidence interval = 1.11-2.15, P = 0.019).
[0039] Table 2
[0040]
[0041]
[0042] The TNM staging sta...
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