Hepatocellular carcinoma: from gene to public health
- PMID: 9414172
- DOI: 10.1093/jnci/89.24.1844
Hepatocellular carcinoma: from gene to public health
Abstract
Liver diseases associated with chronic hepatitis B virus (HBV) infection, including hepatocellular carcinoma, account for more than 1 million deaths annually worldwide. In addition to HBV infection, other risk factors are involved in the etiology of hepatocellular carcinoma and, among these, dietary exposure to the carcinogenic aflatoxins is of particular importance in certain regions of southeast Asia and sub-Saharan Africa. The relative contributions of these two risk factors and the mechanism of the interaction between them in the pathogenesis of hepatocellular carcinoma are still poorly understood. The recently developed individual biochemical and molecular markers of aflatoxin exposure, i.e., aflatoxin-albumin adducts in blood and a specific GC to TA transversion mutation in codon 249 of the p53 gene (249ser p53 mutation) in hepatocellular carcinomas, permit a better quantitative estimation of aflatoxin exposure in different populations of the world. A comprehensive summary of the data from our laboratory and the literature, based on a large number (>1000) of individual cases of hepatocellular carcinoma, is presented here and shows the following: 1) A high level and high prevalence of exposure to aflatoxins occur in West Africa, Mozambique, and some regions of China; 2) a high prevalence of the 249ser p53 mutation is detected in these countries; and 3) hepatocellular carcinomas from countries with low or no exposure to aflatoxins show a very low prevalence of the 249ser p53 mutation and distinctly different p53 mutation spectra, probably indicating different etiologies. Experimental and epidemiologic studies demonstrate an interaction between HBV infection and aflatoxins in hepatocarcinogenesis. The relevance of the biochemical/molecular markers of aflatoxin exposure, HBV vaccination, and the reduction of aflatoxin exposure, in addition to the interaction between HBV infection and other risk factors in liver carcinogenesis, are discussed with regard to the implementation of measures for primary prevention.
Similar articles
-
Dominant role of hepatitis B virus and cofactor role of aflatoxin in hepatocarcinogenesis in Qidong, China.Hepatology. 2002 Nov;36(5):1214-20. doi: 10.1053/jhep.2002.36366. Hepatology. 2002. PMID: 12395332
-
Hepatocellular carcinoma p53 G > T transversions at codon 249: the fingerprint of aflatoxin exposure?Environ Health Perspect. 1997 Apr;105(4):392-7. doi: 10.1289/ehp.97105392. Environ Health Perspect. 1997. PMID: 9189703 Free PMC article.
-
Mutations of p53 gene in hepatocellular carcinoma: roles of hepatitis B virus and aflatoxin contamination in the diet.J Natl Cancer Inst. 1992 Nov 4;84(21):1638-41. doi: 10.1093/jnci/84.21.1638. J Natl Cancer Inst. 1992. PMID: 1279184
-
p53 codon 249ser hot-spot mutation in HBV-negative hepatocellular carcinoma.Lancet. 1993 Jan 23;341(8839):251. doi: 10.1016/0140-6736(93)90124-y. Lancet. 1993. PMID: 8093542 No abstract available.
-
Interactions between hepatitis B virus infection and exposure to aflatoxins in the development of hepatocellular carcinoma: a molecular epidemiological approach.Mutat Res. 1999 Jul 16;428(1-2):187-96. doi: 10.1016/s1383-5742(99)00046-0. Mutat Res. 1999. PMID: 10517992 Review.
Cited by
-
Human Breast Milk Contamination with Aflatoxins, Impact on Children's Health, and Possible Control Means: A Review.Int J Environ Res Public Health. 2022 Dec 14;19(24):16792. doi: 10.3390/ijerph192416792. Int J Environ Res Public Health. 2022. PMID: 36554670 Free PMC article. Review.
-
Tumor suppressor and hepatocellular carcinoma.World J Gastroenterol. 2008 Mar 21;14(11):1720-33. doi: 10.3748/wjg.14.1720. World J Gastroenterol. 2008. PMID: 18350603 Free PMC article. Review.
-
Involvement of DNA damage response pathways in hepatocellular carcinoma.Biomed Res Int. 2014;2014:153867. doi: 10.1155/2014/153867. Epub 2014 Apr 28. Biomed Res Int. 2014. PMID: 24877058 Free PMC article. Review.
-
Histone methyltransferase SETDB1 regulates liver cancer cell growth through methylation of p53.Nat Commun. 2015 Oct 16;6:8651. doi: 10.1038/ncomms9651. Nat Commun. 2015. PMID: 26471002 Free PMC article.
-
Base changes in tumour DNA have the power to reveal the causes and evolution of cancer.Oncogene. 2017 Jan 12;36(2):158-167. doi: 10.1038/onc.2016.192. Epub 2016 Jun 6. Oncogene. 2017. PMID: 27270430 Free PMC article. Review.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Medical
Research Materials
Miscellaneous