Construction method of gene mutation detection library for tumor treatment cardiac toxicity prediction
A technology for cardiotoxicity and tumor treatment, applied in chemical libraries, microbial assay/test, biochemical equipment and methods, etc., can solve problems such as cancer treatment failure
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[0076] The present invention will be described in further detail below in conjunction with the accompanying drawings and specific embodiments.
[0077] Construction method of gene mutation library for prediction of cardiotoxicity in tumor therapy, covering human genes KRAS, JAK3, AKT1, CREBBP, PTEN, RB1, TP53, CTNNB1, TSC2, TSC1, ERBB2, PIK3CA, SF3B1, JAK2, CDH1, SMAD4, GATA3, MAP2K4 A total of 56 genetic variation sites on , MAP3K1 and ESR1.
[0078] Specifically include the following steps:
[0079] (1) For target genes UGT1A6, FANCD2, ABCC5, PIK3R1, SLC22A7, VEGF, GSTA1, SLC22A16, ABCB1, CYP3A5, CYP3A4, SLC28A3, ESR2, AKR1C3, CYP2C8, ABCC2, CAT, GSTP1, SLCO1B3, RARG, SLC22A17, TCL1A, MRP1, ABCC1, NQO1, CYBA, HER2, RAPTOR, CYP2B6, CBR1, NCF4, RAC2, CYP2D6, CBR3, NOS3, ESR1, CELF4 and DPD design the basic amplification primer set, the forward primer and reverse primer set of the basic amplification primer set There are additional 2-5 Ts to the 5' end of the primer, and the ...
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Abstract
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