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The Association Between Cyclooxygenase-2-1195G/A (rs689466) Gene Polymorphism and the Clinicopathology of Lung Cancer in the Japanese Population: A Case-Controlled Study
被引:0
作者:
Sun, Rong
[1
]
Tanino, Ryosuke
[1
]
Tong, Xuexia
[2
]
Isomura, Minoru
[3
]
Chen, Li-Jun
[4
]
Hotta, Takamasa
[1
]
Okimoto, Tamio
[1
]
Hamaguchi, Megumi
[1
]
Hamaguchi, Shunichi
[1
]
Taooka, Yasuyuki
[5
]
Isobe, Takeshi
[1
]
Tsubata, Yukari
[1
]
机构:
[1] Shimane Univ, Fac Med, Dept Internal Med, Div Med Oncol & Resp Med, Shimane, Japan
[2] Ningxia Med Univ, Dept Resp & Crit Care Med, Gen Hosp, Yinchuan, Peoples R China
[3] Shimane Univ, Shimane Univ Fac Med, Dept Pathol, Shimane, Japan
[4] Ningxia Med Univ, Dept Resp Med, Affiliated Hosp 2, Yinchuan, Peoples R China
[5] Med Corp JR Hiroshima Hosp, Dept Resp Med, Div Internal Med, Hiroshima, Japan
关键词:
cyclooxygenase-2;
single nucleotide polymorphism;
promoter region;
lung cancer risk;
squamous cell carcinoma;
Japanese;
OBSTRUCTIVE PULMONARY-DISEASE;
COX-2;
EXPRESSION;
RISK;
OVEREXPRESSION;
COPD;
INFLAMMATION;
VARIANTS;
D O I:
10.3389/fgene.2022.796444
中图分类号:
Q3 [遗传学];
学科分类号:
071007 ;
090102 ;
摘要:
The single nucleotide polymorphisms of COX-2 gene, also known as PTGS2, 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; p = 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.
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页数:8
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