MicroRNA-related polymorphisms in apoptosis pathway genes are predictive of clinical outcome in patients with limited disease small cell lung cancer

被引:4
作者
Jiang, Wei [1 ,2 ]
Bi, Nan [1 ,2 ]
Zhang, Wen-Jue [1 ,2 ]
Wu, Li-Hong [1 ,2 ]
Liu, Li-Pin [1 ,2 ]
Men, Yu [1 ,2 ]
Wang, Jing-Bo [1 ,2 ]
Liang, Jun [1 ,2 ]
Hui, Zhou-Guang [1 ,2 ]
Zhou, Zong-Mei [1 ,2 ]
Wang, Lu-Hua [1 ,2 ]
机构
[1] Chinese Acad Med Sci, Canc Hosp, Dept Radiat Oncol, Beijing 100730, Peoples R China
[2] Peking Union Med Coll, Beijing 100021, Peoples R China
关键词
small cell lung cancer; limited-disease; single nucleotide polymorphisms; microRNA; apoptosis pathway; RADIOTHERAPY; ASSOCIATION; EXPRESSION; MUTATIONS; DISCOVERY; CARCINOMA; CASPASES; TUMORS; DEATH; RISK;
D O I
10.18632/oncotarget.8134
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We examined the impact of single nucleotide polymorphisms (SNPs) at miRNA binding sites in the 3 '-UTRs of genes in the apoptosis pathway on the prognosis of patients with limited disease-small cell lung cancer (LD-SCLC). Twelve tagSNPs in seven genes were genotyped using blood samples from 146 LD-SCLC patients treated with chemoradiotherapy. Cox proportional hazard regression models and recursive partitioning analysis were performed to identify SNPs significantly associated with overall survival. Three SNPs, CASP8: rs1045494 (C>T), PIK3R1: rs3756668 (A>G) and CASP7: rs4353229 (T>C), were associated with longer overall survival in LD-SCLC patients after chemoradiotherapy. The adjusted hazard ratios (95% confidence intervals) were 0.480 (0.258-0.894), 0.405 (0.173-0.947) and 0.446 (0.247-0.802), respectively, and remained significant after multiple comparison correction. Moreover, subset analysis showed these SNPs were still predictive of overall survival in stage III patients. Recursive partitioning analysis enabled patients to be classified into three risk subgroups based on unfavorable genotype combinations of the rs1045494 and rs4353229 SNPs. These findings suggest miRNA-related polymorphisms in the apoptosis pathway may be useful biomarkers for selection of LD-SCLC patients likely to benefit from chemoradiotherapy.
引用
收藏
页码:22632 / 22638
页数:7
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