DNA Repair Gene Variations and Lung Cancer Risk in China
Author Information
Author(s): Bai Yun, Xu Liang, Yang Xiaobo, Hu Zhibin, Yuan Jing, Wang Feng, Shao Minhua, Yuan Wentao, Qian Ji, Ma Hongxia, Wang Ying, Liu Hongliang, Chen Weihong, Yang Lin, Jing Guangfu, Huo Xiang, Chen Feng, Liu Yanhong, Jin Li, Wei Qingyi, Huang Wei, Shen Hongbing, Lu Daru, Wu Tangchun
Primary Institution: Institute of Occupational Medicine and Ministry of Education Key Lab for Environment and Health, School of Public Health, Tongji Medical College, Huazhong University of Science and Technology
Hypothesis
Inherited sequence variations in XPC may alter DNA repair and thus susceptibility to cancer.
Conclusion
Inherited sequence variations in XPC may modulate risk of lung cancer, especially lung adenocarcinoma, in Chinese populations.
Supporting Evidence
- The study found that the rs3731055 AG+AA variant genotypes were associated with a decreased risk of lung adenocarcinoma.
- The haplotype ACCCA was associated with a decreased risk of lung adenocarcinoma but an increased risk of small cell carcinomas.
- The protective effect of rs3731055AG+AA was more evident among young subjects and never smokers.
Takeaway
Some people have changes in their DNA that can make them more or less likely to get lung cancer. This study looked at a group of Chinese people to see how these changes affect their risk.
Methodology
A case-control study with 1,010 lung cancer patients and 1,011 matched controls was conducted to investigate five XPC tagging SNPs.
Potential Biases
Potential selection bias due to low participation rates and DNA sample failures.
Limitations
The study had a relatively low participation rate and some DNA samples failed in genotyping, which may have increased selection bias.
Participant Demographics
All participants were genetically unrelated ethnic Han Chinese.
Statistical Information
P-Value
0.004
Confidence Interval
0.56–0.90
Statistical Significance
p<0.05
Digital Object Identifier (DOI)
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