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Association of CAA and TATC Insertion/Deletion Genetic Polymorphisms in RTN4 3'-UTR with Hepatocellular Carcinoma
NaNa Wang1, KeYu Chen2, Jia Xu1
1School of Medical Laboratory Science, Chengdu Medical College, Chengdu, 610500, China.
Abstract:
Evidence from recent researchers suggested that RTN4 is a multifunctional gene, including tumor suppression, apoptosis, vascular remodeling, and inhibition of axonal regeneration. The CAA and TATC insertion/deletion polymorphisms (CAA/TATC polymorphisms) of RTN4 3″-untranslated regions (UTRs) have been linked to cervical squamous cell carcinoma (CSCC), uterine leiomyomas (UL) and non-small cell lung cancer (NSCLC). However, the association between these two polymorphisms sites with Hepatocellular Carcinoma (HCC) risk was not carry out before. A total of 284 HCC patients and 484 control subjects were recruited for this study. The RTN4 CAA/TATC insertion/deletion genotypes were determined using polymerase chain reaction (PCR) assay. The ID/DD genotypes of CAA were significantly associated with an increased risk of HCC compared with the II genotype (ID vs. II: OR = 1.50, 95% CI: 1.10-2.04; DD vs. II: OR = 2.00, 95%CI: 1.15-3.46). Meanwhile, the frequency of D allele of CAA was significantly related with an increased risk of HCC compared with the I allele (D vs. I: OR = 1.39, 95% CI: 1.12-1.73). The ID genotypes of TATC was significantly associated with an increased risk of HCC compared with the DD genotype (ID vs. DD: OR = 1.70, 95% CI: 1.23-2.33). The present study provided evidence that RTN4 CAA/TATC polymorphisms were associated with HCC development in Chinese Han population.
Insights
Genetic variations in the Reticulon 4 (RTN4) gene, specifically CAA and TATC polymorphisms, are linked to an increased risk of Hepatocellular Carcinoma (HCC). These RTN4 polymorphisms may play a role in HCC development.
Area of Science:
- Genetics
- Oncology
- Molecular Biology
Background:
- Reticulon 4 (RTN4) is a multifunctional gene involved in tumor suppression, apoptosis, vascular remodeling, and axonal regeneration.
- RTN4 3′-untranslated region (UTR) polymorphisms, specifically CAA and TATC insertion/deletion variants, have been associated with cervical squamous cell carcinoma (CSCC), uterine leiomyomas (UL), and non-small cell lung cancer (NSCLC).
Purpose of the Study:
- To investigate the association between RTN4 CAA and TATC insertion/deletion polymorphisms and the risk of Hepatocellular Carcinoma (HCC).
Main Methods:
- Genotyping of RTN4 CAA/TATC insertion/deletion polymorphisms was performed using polymerase chain reaction (PCR) assay.
- A case-control study was conducted with 284 HCC patients and 484 healthy control subjects from the Chinese Han population.
Main Results:
- The ID/DD genotypes of the RTN4 CAA polymorphism were significantly associated with an increased risk of HCC compared to the II genotype (ID vs. II: OR=1.50; DD vs. II: OR=2.00).
- The D allele frequency of the CAA polymorphism was significantly related to an increased HCC risk (D vs. I: OR=1.39).
- The ID genotype of the TATC polymorphism was significantly associated with an increased HCC risk compared to the DD genotype (ID vs. DD: OR=1.70).
Conclusions:
- RTN4 CAA and TATC polymorphisms are associated with an increased risk of Hepatocellular Carcinoma (HCC) development.
- These findings suggest that RTN4 polymorphisms may be potential genetic risk factors for HCC in the Chinese Han population.
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