Differences in genetic susceptibility to tobacco-induced carcinogenesis appear to modulate an individual's risk of squamous-cell carcinoma of the head and neck (SCCHN). Risk for SCCHN may be associated with the null alleles of the carcinogen-metabolizing genes glutathione-S-transferase (GST) T1 and
Polymorphism of Xeroderma Pigmentosum group G and the risk of lung cancer and squamous cell carcinomas of the oropharynx, larynx and esophagus
โ Scribed by Yan Cui; Hal Morgenstern; Sander Greenland; Donald P. Tashkin; Jenny Mao; Wei Cao; Wendy Cozen; Thomas M. Mack; Zuo-Feng Zhang
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- French
- Weight
- 95 KB
- Volume
- 118
- Category
- Article
- ISSN
- 0020-7136
No coin nor oath required. For personal study only.
โฆ Synopsis
Abstract
We investigated the effects of XPG His1104Asp polymorphism (rs17655) on the risk of lung cancer and squamous cell carcinomas of the oropharynx, larynx and esophagus (SCCOLE). This populationโbased caseโcontrol study involves 611 new cases of lung cancer, 601 new cases of oropharyngeal, laryngeal and esophageal cancers, and 1,040 cancerโfree controls. The XPG polymorphism was assayed by PCRโRFLP method for 497 lung cancer cases, 443 cases of oropharyngeal, laryngeal and esophageal cancers and 912 controls. Binary and polytomous unconditional logistic regression models were fitted to assess the main effects and the effect modifications between the polymorphism and environmental exposures. With the adjustment for potential confounders, the XPG Asp1104Asp genotype was inversely associated with lung cancer (odds ratio [OR] = 0.62, 95% confidence limits [CL] = 0.38, 1.0) and SCCOLE (OR = 0.47, 95% CL = 0.27, 0.82), with the combined His1104His and His1104Asp genotypes as the referent. With subjects having genotype Asp1104Asp and no tobacco smoking exposure as the common referent, the ORs on lung cancer were 13 (95% CL = 4.4, 37) for heavy tobacco smoking (>20 packโyears), 1.9 (95% CL = 0.78, 4.5) for having at least one copy of 1104His, and 23 (95% CL = 9.5, 56) for the joint effect, respectively. Compared to nonโsmokers with the Asp1104Asp genotype, the adjusted OR on SCCOLE for heavy smokers (>20 packโyears) having at least one copy of 1104His was 8.0 (95% CL = 2.7, 24). Similarly, compared to nonโdrinkers with the Asp1104Asp genotype, the adjusted OR on SCCOLE for heavy drinkers (โฅ3 drinks/day) with at least one copy of 1104His was 10 (95% CL = 2.7, 38). In conclusion, our study suggests that the XPG Asp1104Asp genotype may be associated with decreased susceptibility to lung cancer and SCCOLE. ยฉ 2005 WileyโLiss, Inc.
๐ SIMILAR VOLUMES
## Abstract The polymorphisms of the tumor suppressor gene p53 have been extensively investigated in numerous malignant tumors, particularly carcinomas associated with human papillomavirus (HPV) infection. However, the results remain controversial. To address a potential correlation between the p53
## Abstract Folate deficiency is implicated in cancer risk that may be modulated by a genetic variation in the methylenetetrahydrofolate reductase (MTHFR) gene in folate metabolism. We hypothesized that genetic variants in __MTHFR__ are associated with risk of squamous cell carcinoma of the head an
## Background: Despite the importance of reactive oxygen species (ros) in the development of smoking-related cancers, little is known about the pattern of expression of ros scavengers in these cancers. ## Methods: In this present study, we examined the expression of manganese superoxide dismutase