[Genetic polymorphism of UDP-glucuronosyltransferase 1F and susceptibility to hepatocellular carcinoma]

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002 Aug;19(4):324-8.
[Article in Chinese]

Abstract

Objective: To study the genetic polymorphisms of UDP-glucuronosyltransferase 1F(UGT1F) and the relationship between polymorphisms and susceptibility to hepatocellular carcinoma (HCC).

Methods: The polymorphisms of UGT1F of 84 patients with HCC and 144 healthy controls were detected by PCR-denaturation gradient gel electrophoresis-sequencing or PCR-single strain conformation polymorphsim-sequencing.

Results: Three new single nucleotide polymorphisms(SNP) were found: the first one was a transversion of TrarrG at nucleotide 232; the second one was the transition of ArarrG at nucleotide 528 in exon 1; the last one was the transition of ArarrG at nucleotide 376 in intron 2. Additionally, the polymorphism at nucleotide 754 was proved in this study. The frequencies of genotype and allele of 4 loci in cases and controls were analyzed. Both frequencies of genotype G/G(13.10%) and allele G (29.17%) of position 754 of UGT1F in cases were sig nificantly greater than those in controls (2.78% and 19.44% ) respectively. For other loci, the difference between the two groups were not significant.

Conclusion: Exons 2-5 of UGT1F are highly conservative, but exon 1 emerges highly polymorphic. And the polymorphism at locus 754 may be related with HCC.

Publication types

  • English Abstract

MeSH terms

  • Alleles
  • Amino Acid Substitution
  • Base Sequence
  • Carcinoma, Hepatocellular / enzymology
  • Carcinoma, Hepatocellular / genetics*
  • DNA Mutational Analysis
  • DNA, Neoplasm / chemistry
  • DNA, Neoplasm / genetics
  • Gene Frequency
  • Genetic Predisposition to Disease / genetics*
  • Genotype
  • Glucuronosyltransferase / genetics*
  • Humans
  • Liver Neoplasms / enzymology
  • Liver Neoplasms / genetics*
  • Odds Ratio
  • Polymorphism, Single Nucleotide*
  • Polymorphism, Single-Stranded Conformational

Substances

  • DNA, Neoplasm
  • Glucuronosyltransferase