The relevance analysis of GSTP1 rs1695 and lung cancer in the Chinese Han population

Author:

Xiao Jiang1,Wang Yulu2,Wang Zhimin3,Zhang Yao1,Li Yutao4,Xu Chang5,Xiao Man6,Wang Haijian4,Guo Shicheng7,Jin Li48,Wang Jiucun48,Bao Yang9,Shang Yan110,Wu Junjie14ORCID

Affiliation:

1. Department of Respiratory and Critical Care Medicine, The First Affiliated Hospital of Naval Medical University, Shanghai, China

2. Department of Emergency, Tongde Hospital of Zhejiang Province, Hangzhou, China

3. Shanghai-MOST key Laboratory of Heath and Disease Genomics, Chinese National Human Genome Center at Shanghai (CHGC) and Shanghai Institute for Biomedical and Pharmaceutical Technologies (SIBPT), Shanghai, China

4. Ministry of Education Key Laboratory of Contemporary Anthropology and State Key Laboratory of Genetic Engineering, Collaborative Innovation Center for Genetics and Development, School of Life Sciences, Fudan University, Shanghai, China

5. Clinical College of Xiangnan University, Chenzhou, China

6. Department of Biochemistry and Molecular Biology, Hainan Medical University, Haikou, China

7. Department of Medical Genetics, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI, USA

8. Human Phenome Institute, Fudan University, Shanghai, China

9. Department of Cardiothoracic Surgery, Affiliated Hospital of Yangzhou University, Yangzhou, China

10. Department of General Practice, The First Affiliated Hospital of Naval Medical University, Shanghai, China

Abstract

Background This study explored the relevance between rs1695 and susceptibility to the lung cancer in the Chinese Han population. Stratification analysis was conducted on the basis of age, gender, smoking status, tumor-related family history, and pathological type to observe relations between rs1695 and susceptibility to lung cancer in the subgroups. Methods A case-control study was performed with 974 lung cancer patients who were pathologically diagnosed and 1005 healthy cases based on physical examination to analyze the association between rs1695 and the risk of lung cancer. Results The frequencies of the AA, GA, and GG genotypes of rs1695 were 68.4%, 28.7%, and 2.9% in cases and 64.8%, 30.8%, and 4.2% in controls, respectively. After adjustment for age, gender, smoking status, and family history, it appears that the rs1695 G allele decreases the risk of lung cancer (OR = 0.811, 95% CI 0.684–0.961, P = 0.016). Moreover, compared with the AA genotype, the GA + GG genotype decreased lung cancer susceptibility (OR = 0.808, 95% CI 0.663–0.985, P = 0.035) and the GG genotype (OR = 0.591, 95% CI 0.347–0.988, P = 0.048). In a stratified analysis, the risk of lung cancer in the G allele carriers decreased among the males, patients without a tumor-related family history, and patients with lung adenocarcinoma, especially in smokers. Conclusion The polymorphism of locus rs1695 is related to the risk of lung cancer and is expected to be a target for the prediction of lung cancer.

Funder

Shanghai Changhai Hospital Scientific Research Fund

Shanghai Postdoctoral Science Foundation

National Natural Science Foundation of China

Publisher

SAGE Publications

Subject

Cancer Research,Clinical Biochemistry,Oncology,Pathology and Forensic Medicine

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