Relationship between HLA-DRB1 allele polymorphisms and familial aggregations of hepatocellular carcinoma

S Ma1, J Wu1, J Wu1

  • 1Department of Infectious Diseases, First Affiliated Hospital of Guangxi Medical University, Nanning, P.R.C.

Insights

Genetic factors in familial hepatocellular carcinoma (fhcc) may involve specific HLA-DRB1 alleles. Lower frequencies of DRB1*11 and DRB1*12 alleles were observed in fhcc families, suggesting a potential risk factor.

Area of Science:

  • Immunogenetics
  • Cancer Epidemiology
  • Human Leukocyte Antigen (HLA) System

Background:

  • Familial aggregation of hepatocellular carcinoma (fhcc) suggests a potential genetic component.
  • The Human Leukocyte Antigen (HLA) system, particularly HLA-DRB1 alleles, plays a crucial role in immune response and has been implicated in various cancers.

Purpose of the Study:

  • To investigate the association between HLA-DRB1 allele polymorphisms and the familial aggregation of hepatocellular carcinoma (fhcc).

Main Methods:

  • Genotyping of HLA-DRB1 alleles was performed using polymerase chain reaction sequence-specific primers.
  • 130 members from families with multiple liver cancer patients and 130 members from cancer-free families were analyzed.
  • Genotype frequencies were compared between the fhcc and no-cancer groups.

Main Results:

  • The frequencies of HLA-DRB1*11 and HLA-DRB1*12 alleles were significantly lower in the fhcc group compared to the no-cancer group (p < 0.05).
  • Odds ratios for DRB1*11 and DRB1*12 were 0.286 and 0.493, respectively, indicating a potential protective effect or reduced risk.
  • No statistically significant differences in the frequencies of the other nine studied HLA-DRB1 alleles were found between the groups.

Conclusions:

  • The study suggests that a deficiency in HLA-DRB1*11 and HLA-DRB1*12 alleles may represent a genetic risk factor for fhcc in the Guangxi Zhuang Autonomous Region.
  • These findings contribute to understanding the genetic underpinnings of fhcc and highlight specific HLA-DRB1 alleles for further investigation.
Abstract

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