Effect of RECK gene polymorphisms on hepatocellular carcinoma susceptibility and clinicopathologic features
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 carci...
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Published in | PloS one Vol. 7; no. 3; p. e33517 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Public Library of Science
12.03.2012
Public Library of Science (PLoS) |
Subjects | |
Online Access | Get full text |
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Summary: | 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.
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.
RECK gene polymorphisms might be a risk factor increasing HCC susceptibility and distant metastasis in Taiwan. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 Conceived and designed the experiments: TC SY. Performed the experiments: MC YH SY. Analyzed the data: SS CY. Contributed reagents/materials/analysis tools: TC YL SY. Wrote the paper: YH SY. |
ISSN: | 1932-6203 1932-6203 |
DOI: | 10.1371/journal.pone.0033517 |