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Genetic Variant of Notch Regulator DTX1 Predicts Survival After Lung Cancer Surgery

Authors
Lee, Jang HyuckShin, Kyung MinLee, Shin YupHong, Mi JeongChoi, Jin EunKang, Hyo-GyoungDo, Sook KyungLee, Won KeeLee, Eung BaeSeok, YangkiJeong, Ji YunYoo, Seung SooLee, JaeheeCha, Seung IckKim, Chang HoCho, SukkiJheon, SanghoonKim, Young ChulOh, In JaeNa, Kook JooKim, Moon SooLee, Jong MogYang, Hee ChulJung, Chi YoungPark, Chang KwonLee, Min KiKim, Dong KwanPark, Jae Yong
Issue Date
Oct-2019
Publisher
Lippincott Williams & Wilkins Ltd.
Keywords
DTX1; lung cancer; survival
Citation
Annals of Surgical Oncology, v.26, no.11, pp 3756 - 3764
Pages
9
Journal Title
Annals of Surgical Oncology
Volume
26
Number
11
Start Page
3756
End Page
3764
URI
https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/4196
DOI
10.1245/s10434-019-07614-2
ISSN
1068-9265
1534-4681
Abstract
Background We evaluated the association between genetic variants in the Notch pathway and survival outcomes of patients with surgically resected NSCLC. Methods Sixty-four single nucleotide polymorphisms (SNPs) in the Notch pathway genes were evaluated in the discovery study (n = 354) and two sequential validation studies (n = 772 and n = 746, respectively). The association of genotype with overall survival (OS) and disease-free survival (DFS) was evaluated. Results Of the 64 SNPs analyzed in the discovery study, 9 were significantly associated with OS or DFS. Among them, the association remained significant only for Deltex-1 (DTX1) rs1732786A>G in the first validation study. The second validation study confirmed again the association between DTX1 rs1732786A>G and survival outcomes. In the combined analysis, rs1732786A>G was significantly associated with better OS and DFS (adjusted HR center dot aHR center dot for OS, 0.75; 95% CI 0.64-0.87; P = 0.0002; aHR for DFS, 0.79; 95% CI 0.71-0.89; P = 0.0001). In vitro luciferase assay showed that the rs1732786G allele was associated with higher promoter activity compared to rs1732786A allele. Consistently, relative mRNA expression level of DTX1 showed significant positive correlation with rs1732786 A-to-G change (P-trend = 0.02) in tumor tissues. Conclusions These results suggest that DTX1 rs1732786 is a potential prognostic factor that may have clinical utility in the management of early stage NSCLC.
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