Abstract

Background: Unlike with esophageal cancer, acetaldehyde levels and genetic polymorphisms in alcohol dehydrogenase have not yet been shown to be contributing factors for colorectal cancer (CRC). This study aimed to clarify the mechanism of CRC development related to alcohol consumption and to the presence of genetic polymorphisms in the alcohol dehydrogenase, ADH1B and aldehyde dehydrogenase, ALDH2. Methods: This was a case-control study (221 cases and 179 controls) in patients with adenomas and intramucosal tumors who underwent endoscopic removal of all tumors. The amount of alcohol consumption was determined using a self-recorded questionnaire, and the tumor information was obtained from colonoscopy results. Blood samples were taken to analyze the following polymorphisms: ALDH2 Glu504Lys and ADH1B His48Arg. Results: The polymorphisms in ADH1B and ALDH2 had little influence on the development of colorectal adenoma or intramucosal cancer. Patients with ALDH2 (Glu/Glu) were more tolerant of alcohol than those with ALDH2 (Glu/Lys and Lys/Lys). Next, we examined certain combinations of the ADH1B genotypes. In the ALDH2 (Glu/Glu) group, an increased risk (OR = 3.4; 95% CI 1.4 - 8.4; P = 0.009) was observed among moderate/heavy drinkers with ADH1B (His/His). In the ALDH2 (Glu/Lys and Lys/Lys) group, an increased risk (OR = 4.2; 95% CI 1.1 - 16.7; P = 0.041) was found among moderate/heavy drinkers with ADH1B (Arg/His and Arg/Arg). Conclusions: ADH1B and ALDH2 activity may be involved in the development of CRC.

Highlights

  • Many epidemiological studies have confirmed that alcohol consumption is strongly associated with the development of colorectal cancer (CRC) [1]

  • The participants included 445 male and female patients aged 40 to 65 years who had undergone a total colonoscopy at Osaka Medical Center for Cancer and Cardiovascular Diseases, a hospital located in the city of Osaka, Japan, in which two or more colorectal tumors were identified; these patients subsequently underwent the endoscopic removal of all tumors

  • Comparisons between the Case Group and Control Group regarding the amount of alcohol intake, smoking and genotype were performed by calculating the odds ratio (OR) and 95% confidence interval (CI)

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Summary

Introduction

Many epidemiological studies have confirmed that alcohol consumption is strongly associated with the development of colorectal cancer (CRC) [1]. With regard to esophageal cancer, the involvement of acetaldehyde, a metabolite of alcohol, has been implicated in the carcinogenesis of esophageal cancer based on studies of genetic polymorphisms in ALDH2 [7]-[11]. Acetaldehyde levels and genetic polymorphisms in alcohol dehydrogenase have not yet been shown to be contributing factors for colorectal cancer (CRC). This study aimed to clarify the mechanism of CRC development related to alcohol consumption and to the presence of genetic polymorphisms in the alcohol dehydrogenase, ADH1B and aldehyde dehydrogenase, ALDH2. Blood samples were taken to analyze the following polymorphisms: ALDH2 Glu504Lys and ADH1B His48Arg. Results: The polymorphisms in ADH1B and ALDH2 had little influence on the development of colorectal adenoma or intramucosal cancer.

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