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Published on: September 30, 2021
Effect of RECK gene polymorphisms on hepatocellular carcinoma susceptibility and clinicopathologic features
Tsung-Te Chung1, Chao-Bin Yeh, Yi-Ching Li
1Institute of Medicine, Chung Shan Medical University, Taichung, Taiwan.
Background:
The reversion-inducing-cysteine-rich protein with Kazal motifs (RECK) down-regulation has been confirmed in numerous human cancers and is clinically associated with metastasis. This study investigates the potential associations of RECK single-nucleotide polymorphisms (SNPs) with hepatocellular carcinoma (HCC) susceptibility and its clinicopathologic characteristics.
Methodology/Principal Findings:
A total of 135 HCC cancer patients and 501 cancer-free controls were analyzed for four RECK SNPs (rs10814325, rs16932912, rs11788747, and rs10972727) using real-time PCR and PCR-RFLP genotyping analysis. After adjusting for other co-variants, the individuals carrying RECK promoter rs10814325 inheriting at least one C allele had a 1.85-fold [95% confidence interval (CI), 1.03-3.36] risk of developing HCC compared to TT wild type carriers. The HCC patients, who carried rs11788747 with at least one G allele, had a higher distant metastasis risk than wild type probands.
Conclusions:
RECK gene polymorphisms might be a risk factor increasing HCC susceptibility and distant metastasis in Taiwan.
Insights
Genetic variations in the RECK gene, specifically certain single-nucleotide polymorphisms (SNPs), are linked to an increased risk of developing hepatocellular carcinoma (HCC) and its distant metastasis. These RECK gene polymorphisms may serve as a risk factor in Taiwan.
Area of Science:
- Genetics
- Oncology
- Molecular Biology
Background:
- Reversion-inducing-cysteine-rich protein with Kazal motifs (RECK) is frequently downregulated in various cancers.
- RECK down-regulation correlates with increased metastasis in human cancers.
- The role of RECK genetic variations in hepatocellular carcinoma (HCC) remains underexplored.
Purpose of the Study:
- To investigate the association between RECK single-nucleotide polymorphisms (SNPs) and hepatocellular carcinoma (HCC) susceptibility.
- To explore the correlation of RECK SNPs with clinicopathologic characteristics of HCC.
Main Methods:
- Genotyping analysis of four RECK SNPs (rs10814325, rs16932912, rs11788747, and rs10972727) in 135 HCC patients and 501 controls.
- Utilized real-time PCR and PCR-RFLP for SNP genotyping.
- Statistical analysis adjusted for relevant co-variants.
Main Results:
- Individuals with the RECK promoter rs10814325 C allele showed a 1.85-fold increased risk of HCC (95% CI, 1.03-3.36).
- HCC patients carrying the rs11788747 G allele exhibited a higher risk of distant metastasis compared to wild-type carriers.
- No significant association was found for rs16932912 and rs10972727.
Conclusions:
- RECK gene polymorphisms, particularly rs10814325 and rs11788747, are potential risk factors for HCC susceptibility and distant metastasis.
- These findings suggest RECK SNPs could serve as biomarkers for HCC risk and progression in the Taiwanese population.
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