Genetic changes and expression of the mannose 6-phosphate/insulin-like growth factor II receptor gene in human hepatitis B virus-associated hepatocellular carcinoma
pmid: 12736721
Genetic changes and expression of the mannose 6-phosphate/insulin-like growth factor II receptor gene in human hepatitis B virus-associated hepatocellular carcinoma
It was reported that 60-70% of hepatitis B virus (HBV)-negative hepatocellular carcinoma (HCC) had loss of heterozygosity (LOH) at the mannose 6-phosphate/insulin-like growth factor II receptor (M6P/IGF2R) locus and this gene was mutated in 55% of these patients with LOH. In this study, genomic DNA from 29 pairs of HBV-positive HCC and corresponding non-tumor tissues was used to analyze LOH at the M6P/IGF2R locus and single deoxyguanosine deletion in this gene by PCR. Total RNA from 19 of the 29 patients was utilized to determine a 192 bp insert in the M6P/IGF2R mRNA and expression of this gene by RT-PCR. Twenty-eight of 29 (97%) HBV-positive HCC were found to be informative at the M6P/IGF2R locus but LOH at this region was only detected in 4/28 (14%) informative patients. Neither single deoxyguanosine deletion in this gene nor 192 bp insert in its mRNA occurred in these patients. Compared with corresponding non-tumor tissues, expression of the M6P/IGF2R mRNA was decreased in 13/19 (68%) HBV-positive HCC tissues, suggesting that M6P/IGF2R may be involved in HBV-associated hepatocarcinogenesis by the regulation of its expression level. In the development of HBV-associated HCC, M6P/IGF2R mutation may not be a major agent.
- Singapore General Hospital Singapore
Adult, Male, Carcinoma, Hepatocellular, DNA, Complementary, Base Sequence, Liver Neoplasms, Gene Expression, Loss of Heterozygosity, Middle Aged, Hepatitis B, Receptor, IGF Type 2, Mutation, Humans, Female, RNA, Messenger, RNA, Neoplasm
Adult, Male, Carcinoma, Hepatocellular, DNA, Complementary, Base Sequence, Liver Neoplasms, Gene Expression, Loss of Heterozygosity, Middle Aged, Hepatitis B, Receptor, IGF Type 2, Mutation, Humans, Female, RNA, Messenger, RNA, Neoplasm
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