An expression quantitative trait locus variant for LKB1 gene predicts the clinical outcomes of chemotherapy in patients with non-small cell lung cancer

被引:3
作者
Seo, Hyewon [1 ]
Jung, Deuk Kju [2 ,3 ]
Kang, Hyo-Gyoung [2 ,3 ]
Jeong, Ji Yun [4 ]
Lee, Shin Yup [1 ,5 ]
Choi, Jin Eun [2 ,3 ]
Hong, Mi Jeong [2 ,3 ]
Do, Sook Kyung [2 ,6 ]
Lee, Jang Hyuck [2 ,6 ]
Lee, Won Kee [7 ,8 ]
Shin, Kyung Min [9 ]
Yoo, Seung Soo [1 ,5 ]
Lee, Jaehee [1 ]
Cha, Seung Ick [1 ]
Kim, Chang Ho [1 ]
Park, Jae Yong [1 ,2 ,3 ,5 ,6 ]
机构
[1] Kyungpook Natl Univ, Sch Med, Dept Internal Med, Daegu, South Korea
[2] Kyungpook Natl Univ, Sch Med, Dept Biochem & Cell Biol, Daegu, South Korea
[3] Kyungpook Natl Univ, Sch Med, Cell & Matrix Res Inst, Daegu, South Korea
[4] Kyungpook Natl Univ, Sch Med, Dept Pathol, Daegu, South Korea
[5] Kyungpook Natl Univ, Chilgok Hosp, Lung Canc Ctr, Daegu, South Korea
[6] Kyungpook Natl Univ, Dept Biomed Sci, BK21 Plus KNU Biomed Convergence Program, Daegu, South Korea
[7] Kyungpook Natl Univ, Kyungpook Natl Univ Hosp, Med Res Collaborat Ctr, Daegu, South Korea
[8] Kyungpook Natl Univ, Sch Med, Daegu, South Korea
[9] Kyungpook Natl Univ, Sch Med, Dept Radiol, Daegu, South Korea
基金
新加坡国家研究基金会;
关键词
Lung cancer; Polymorphism; RegulomeDB; Chemotherapy response; Survival; PACLITAXEL; ASSOCIATION; METABOLISM; APOPTOSIS; SURVIVAL; LESSONS; KINASE;
D O I
10.1016/j.cancergen.2018.10.002
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: We conducted this study to identify regulatory variants in cancer-related pathway genes which can predict clinical outcomes of chemotherapy in advanced NSCLC, using a comprehensive list of regulatory SNPs prioritized by RegulomeDB. Methods: A total of 509 potentially functional SNPs in cancer-related pathway genes were evaluated. The SNPs were analyzed in a discovery set (n=198), and an independent validation set (n=181). The associations of the SNPs with chemotherapy response and overall survival (OS) were analyzed. Results: In the discovery set, 95 SNPs were significantly associated with clinical outcomes. Among the 95 SNPs, only rs10414193A > G in the intronic region of ARID3A, an eQTL for LKB1, was consistently associated with chemotherapy response and OS in the validation set. In combined analysis, the rs10414193A > G was significantly associated with worse response to chemotherapy (adjusted odds ratio = 0.63, 95% CI = 0.47-0.85, P = 0.002), and with worse OS (adjusted hazard ratio = 1.25, 95% CI = 1.08-1.45, P = 0.004). Luciferase assay showed a significantly higher LKB1 promoter activity associated with rs10414193G allele compared with rs10414193A allele (P = 0.0009). Conclusions: Our results suggest that rs10414193A > G may be useful for the prediction of clinical outcomes of chemotherapy in advanced NSCLC.
引用
收藏
页码:73 / 82
页数:10
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