4.7 Article

Interaction between interleukin-1β-31T/C gene polymorphism and drinking and smoking habits on the risk of hepatocellular carcinoma among Japanese

Journal

CANCER LETTERS
Volume 271, Issue 1, Pages 98-104

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.canlet.2008.05.036

Keywords

Hepatocellular carcinoma; Interleukin-1 beta; Tumor necrosis factor-alpha; Alcohol; Smoking; Case-control study

Categories

Funding

  1. Ministry of Education, Culture, Sports, Science and Technology [11670344, 13220014, 14031216, 15390188]
  2. Ministry of Health, Labor and Welfare, Japan
  3. Grants-in-Aid for Scientific Research [13220014, 15390188, 14031216, 11670344] Funding Source: KAKEN

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The risk of hepatocellular carcinoma (HCC) increases with the severity of hepatic inflammation. Interleukin (IL)-1 beta and tumor necrosis factor (TNF)-alpha are proinflammatory cytokines with multiple biological effects and may play essential roles in inflammation-linked tumor development. We conducted a case-control study including 209 incident HCC cases and two control groups (275 hospital controls and 381 patients with chronic liver disease [CLD] without HCC) to investigate whether IL-1B and TNF-A gene polymorphisms influence HCC susceptibility with any interaction with alcohol and tobacco. By comparing HCC cases with CLD patients, we found that IL-1B -31T/C polymorphism was associated with HCC risk among never drinkers and current smokers; adjusted odds ratios (and 95% confidence intervals) for C/T and T/(sic). genotypes compared with C/C genotype were 1.70 (0.76-3.77) and 2.46 (1.05-5.76) (P trend = 0.03), respectively, among never drinkers, and 1.53 (0.60-3.99) and 2.54 (0.81-7.95) (P trend = 0.11), respectively, among current smokers. Similarly HCC risk associated with heavy alcohol intake and current smoking differed by this polymorphism among CLD patients IL-1B -31T/C polymorphism may modify HCC risk in relation to alcohol intake or smoking. (C) 2008 Elsevier Ireland Ltd. All rights reserved.

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