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Relationship between HLA-DRB1 allele polymorphisms and familial aggregations of hepatocellular carcinoma
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.
Objective:
We explored the relationship between HLA-DRB1 allele polymorphisms and familial aggregation of hepatocellular carcinoma (fhcc).
Methods:
Polymerase chain reaction sequence-specific primers were used to determine HLA-DRB1 genotypes for 130 members of families with 2 or more liver cancer patients and for 130 members of families without any diagnosed cancers. The genotype profiles were then compared to explore the relationship between HLA-DRB1 gene polymorphism and fhcc.
Result:
Of 11 selected alleles, the frequencies of DRB1*11 and DRB1*12 were significantly lower in the fhcc group than in no-cancer group (p < 0.05; odds ratio: 0.286; 95% confidence interval: 0.091 to 0.901; and odds ratio: 0.493; 95% confidence interval: 0.292 to 0.893). Differences in the frequencies of the other 9 alleles were not statistically significant in the two groups (p > 0.05).
Conclusions:
Our research suggests that if genetic factors play a role in fhcc, the deficiency in the DRB1*11 and DRB1*12 alleles might be the risk factor at work in Guangxi Zhuang Autonomous Region, P.R.C.
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