作者: Datong Zheng , Yanping Chen , Caijie Gao , Yongyue Wei , Guochun Cao
DOI: 10.4161/15384047.2014.956599
关键词:
摘要: Adverse events in platinum-based chemotherapy for patients with advanced non-small cell lung cancer (NSCLC) are major challenges. In this study, we investigated the role of p53 and MDM2 genes predicting adverse NSCLC treated chemotherapy. Specifically, examined p. Pro72Arg (rs1042522), c.14 + 309T>G (rs2279744) c.− 461C > G (rs937282) polymorphisms using PCR-based restriction fragment length polymorphism (RFLP) 444 patients. We determine that 309T was significantly associated severe hematologic overall toxicities chemotherapy, especially aged 57 younger. This also true adenocarcinoma. Second, gastrointestinal heterozygous c.−461C were higher than G/G genotype. Third, − CT haplotype show much those CG haplotype. Moreover, carrying c.−461 –c.14 CG/CT diplotype exhibited CG/CG. Fourth, found interacts both age addition, no significant associations observed between 3 SNPs response to first-line summary, Pro72Arg, toxicity risks following treatment suggest may be used as a candidate biomarker predict who had treatment.