18.190.176.176
18.190.176.176
close menu
An eQTL variant for LKB1 gene and the clinical outcomes of chemotherapy in non-small cell lung cancer
서혜원 , ( Deuk Kju Jung ) , ( Hyo-gyoung Kang ) , ( Shin Yup Lee ) , ( Jin Eun Choi ) , ( Mi Jeong Hong ) , ( Sook Kyung Do ) , ( Jang Hyuck Lee ) , ( Seung Soo Yoo ) , ( Jaehee Lee ) , ( Seung Ick Cha ) , ( Chang Ho Kim ) , ( Jae Yong Park )
UCI I410-ECN-0102-2019-500-001723271
이 자료는 4페이지 이하의 자료입니다.
* 발행 기관의 요청으로 무료로 이용 가능한 자료입니다.

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.

[자료제공 : 네이버학술정보]
×