MDM2 SNP309 Contributes to Non-Small Cell Lung Cancer Survival in Chinese

被引:20
|
作者
Dong, Jing [2 ]
Ren, Binhui [3 ]
Hu, Zhibin [2 ,4 ]
Chen, Jiaping [2 ]
Hu, Lingmin [2 ]
Dai, Juncheng [2 ]
Jin, Guangfu [2 ]
Xu, Lin [3 ]
Shen, Hongbing [1 ,2 ,4 ]
机构
[1] Nanjing Med Univ, Dept Epidemiol & Biostat, Ctr Canc, Sch Publ Hlth,Key Lab Modern Toxicol, Nanjing 210029, Peoples R China
[2] Nanjing Med Univ, Minist Educ, Key Lab Modern Toxicol, Sch Publ Hlth, Nanjing 210029, Peoples R China
[3] Jiangsu Canc Hosp, Dept Thorac Surg, Nanjing, Peoples R China
[4] Nanjing Med Univ, Dept Clin Epidemiol, Ctr Canc, Nanjing 210029, Peoples R China
基金
中国国家自然科学基金;
关键词
MDM2; polymorphisms; NSCLC; prognosis; SINGLE NUCLEOTIDE POLYMORPHISM; GENETIC POLYMORPHISMS; ONCOPROTEIN MDM2; P53; PATHWAY; RISK; ASSOCIATION; PROMOTER; PROTEIN; SUSCEPTIBILITY; EPIDEMIOLOGY;
D O I
10.1002/mc.20727
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Murine double minute 2 (MDM2) is a negative regulator of the tumor suppressor gene p53. Single nucleotide polymorphisms in MDM2 and p53 can affect patient's response to chemotherapy as well as overall survival of many cancers. This study aimed to assess the associations between polymorphisms in MDM2 and p53 and survival of non-small cell lung cancer (NSCLC) patients in Chinese. We selected and genotyped both potentially functional SNPs and tagging SNPs in MDM2 and p53 using Illumina Golden Gate platform in a cohort of 568 NSCLC patients. Associations between genotypes and NSCLC median survival time (MST) were assessed using the Kaplan-Meier method. Cox proportional hazard models were performed with the adjustment for age, stage, smoking, histology, surgical operation, and chemo-or radiotherapy status. We found that the MDM2 SNP309 (rs2279744) GT/TT genotypes were associated with a significantly worse survival (MST: 23.0 mo for GT/TT vs. 33.0 mo for GG; log-rank P = 0.028). In the multivariate Cox regression analyses, the MDM2 SNP309GT/TT genotypes were associated with a 1.42-fold [HR = 1.42,95% confidence interval (CI), 1.09-1.84] increased risk of death of NSCLC, compared with SNP309GG genotype. MDM2 SNP309 may be used as one of the candidate biomarkers to predict NSCLC survival. (C) 2011 Wiley-Liss, Inc.
引用
收藏
页码:433 / 438
页数:6
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