» Articles » PMID: 35450217

The Association Between Cyclooxygenase-2 -1195G/A (rs689466) Gene Polymorphism and the Clinicopathology of Lung Cancer in the Japanese Population: A Case-Controlled Study

Overview
Journal Front Genet
Date 2022 Apr 22
PMID 35450217
Authors
Affiliations
Soon will be listed here.
Abstract

The single nucleotide polymorphisms of COX-2 gene, also known as , which encodes a pro-inflammatory factor cyclooxygenase-2, alter the risk of developing multiple tumors, but these findings are not consistent for lung cancer. We previously reported that the homozygous COX-2 -1195A genotype is associated with an increased risk for chronic obstructive pulmonary disease (COPD) in Japanese individuals. COPD is a significant risk factor for lung cancer due to genetic susceptibility to cigarette smoke. In this study, we investigated the association between COX-2 -1195G/A polymorphism and lung cancer susceptibility in the Japanese population. We evaluated the genotype distribution of COX-2 -1195G/A using a polymerase chain reaction-restriction fragment length polymorphism assay for 330 newly diagnosed patients with lung cancer and 162 healthy controls. Our results show that no relationship exists between the COX-2 -1195G/A polymorphism and the risk of developing lung cancer. However, compared to the control group, the homozygous COX-2 -1195A genotype increased the risk for lung squamous cell carcinoma (odds ratio = 2.902; 95% confidence interval, 1.171-7.195; = 0.021), whereas no association is observed with the risk for adenocarcinoma. In addition, Kaplan-Meier analysis shows that the genotype distribution of homozygous COX-2 -1195A does not correlate with the overall survival of patients with lung squamous cell carcinoma. Thus, we conclude that the homozygous COX-2 -1195A genotype confers an increased risk for lung squamous cell carcinoma in Japanese individuals and could be used as a predictive factor for early detection of lung squamous cell carcinoma.

Citing Articles

COX-2 in lung cancer: Mechanisms, development, and targeted therapies.

Liu X, Zhang J, Sun W, Cao J, Ma Z Chronic Dis Transl Med. 2024; 10(4):281-292.

PMID: 39429482 PMC: 11483542. DOI: 10.1002/cdt3.120.

References
1.
Young R, Hopkins R . How the genetics of lung cancer may overlap with COPD. Respirology. 2011; 16(7):1047-55. DOI: 10.1111/j.1440-1843.2011.02019.x. View

2.
Chen L, Xu W, Taooka Y, Ohe M, Takahashi H, Sutani A . Cyclooxygenase 2 1195G > A polymorphism is associated with chronic obstructive pulmonary disease in Japanese and Chinese patients. Chin Med J (Engl). 2013; 126(12):2215-21. View

3.
Liu C, Chang S, Narko K, Trifan O, Wu M, Smith E . Overexpression of cyclooxygenase-2 is sufficient to induce tumorigenesis in transgenic mice. J Biol Chem. 2001; 276(21):18563-9. DOI: 10.1074/jbc.M010787200. View

4.
Li M, Li M, Wei Y, Xu H . Prognostic and Clinical Significance of Cyclooxygenase-2 Overexpression in Endometrial Cancer: A Meta-Analysis. Front Oncol. 2020; 10:1202. PMC: 7438859. DOI: 10.3389/fonc.2020.01202. View

5.
Patti R, Gumired K, Reddanna P, Sutton L, Phillips P, Reddy C . Overexpression of cyclooxygenase-2 (COX-2) in human primitive neuroectodermal tumors: effect of celecoxib and rofecoxib. Cancer Lett. 2002; 180(1):13-21. DOI: 10.1016/s0304-3835(02)00003-4. View