| International Journal of Molecular Sciences | |
| Ping He5  Xue-Xi Yang1  Xuan-Qiu He3  Jun Chen4  Fen-Xia Li6  Xia Gu5  Ju-Hong Jiang5  Hui-Ying Liang2  Guang-Yu Yao4  | |
| [1] School of Biotechnology, Southern Medical University, Guangzhou 510515, China; E-Mail:;Department of Primary Public Health, Guangzhou Center for Disease Control and Prevention, Guangzhou 510440, China; E-Mail:;The First Clinical College, Southern Medical University, Guangzhou 510515, China; E-Mail:;Breast Center, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China; E-Mails:;Department of Pathology, the First Affiliated Hospital of Guangzhou Medical University, Guangzhou 510120, China; E-Mails:;Da An Gene Co., Ltd. of Sun Yat-sen University, Guangzhou 510665, China; E-Mail: | |
| 关键词:
lung adenocarcinoma;
single nucleotide polymorphism;
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| DOI : 10.3390/ijms15045446 | |
| 来源: mdpi | |
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【 摘 要 】
Recent genome-wide association studies (GWASs) have identified 15q25.1 as a lung cancer susceptibility locus. Here, we sought to explore the direct carcinogenic effects of genetic variants in this region on the risk of developing lung adenocarcinoma (ADC). Five common SNPs (rs8034191, rs16969968, rs1051730, rs938682, and rs8042374) spanning the 15q25.1 locus were assayed in a case-control study examining a cohort of 301 lung ADCs and 318 healthy controls. Stratification analysis by gender, smoking status, and tumor, node, metastasis (TNM) classification, was performed. In addition, sections from ADC tissue and normal tissue adjacent to tumors were stained with an anti-CHRNA3 (cholinergic receptor nicotinic α3) antibody by immunohistochemistry in 81 cases. Our results demonstrate that rs8042374, a variant of the
【 授权许可】
CC BY
© 2014 by the authors; licensee MDPI, Basel, Switzerland
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| Files | Size | Format | View |
|---|---|---|---|
| RO202003190027433ZK.pdf | 1078KB |
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