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A Genetic Variant in the Promoter Region of miR-106b-25 Cluster Predict Clinical Outcome of HBV-Related Hepatocellular Carcinoma in Chinese

BACKGROUND: MiR-106b-25 cluster, hosted in intron 13 of MCM7, may play integral roles in diverse processes including immune response, tumorigenesis and progression. A single nucleotide polymorphism (SNP), rs999885, is located in the promoter region of MCM7. Our previous study showed that the A to G...

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Autores principales: Qi, Fuzhen, Huang, Mingde, Pan, Yun, Liu, Yao, Liu, Jibin, Wen, Juan, Xie, Kaipeng, Shen, Hongbing, Ma, Hongxia, Miao, Yi, Hu, Zhibin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3885710/
https://www.ncbi.nlm.nih.gov/pubmed/24416400
http://dx.doi.org/10.1371/journal.pone.0085394
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author Qi, Fuzhen
Huang, Mingde
Pan, Yun
Liu, Yao
Liu, Jibin
Wen, Juan
Xie, Kaipeng
Shen, Hongbing
Ma, Hongxia
Miao, Yi
Hu, Zhibin
author_facet Qi, Fuzhen
Huang, Mingde
Pan, Yun
Liu, Yao
Liu, Jibin
Wen, Juan
Xie, Kaipeng
Shen, Hongbing
Ma, Hongxia
Miao, Yi
Hu, Zhibin
author_sort Qi, Fuzhen
collection PubMed
description BACKGROUND: MiR-106b-25 cluster, hosted in intron 13 of MCM7, may play integral roles in diverse processes including immune response, tumorigenesis and progression. A single nucleotide polymorphism (SNP), rs999885, is located in the promoter region of MCM7. Our previous study showed that the A to G base change of rs999885 may provide an increased risk for HCC in HBV persistent carriers by altering the expression of the miR-106b-25 cluster. However, it is unknown whether rs999885 is associated with prognosis of intermediate or advanced HBV-related hepatocellular carcinoma (HCC) patients. METHODS: The SNP, rs999885, was genotyped by using the TaqMan allelic discrimination Assay in 414 intermediate or advanced HCC patients. Log-rank test and Cox proportional hazard models were used for survival analysis. RESULTS: The variant genotypes of rs999885 were associated with a significantly decreased risk of death for intermediate or advanced HCC [additive model: adjusted hazard ratio (HR)  = 0.76,95% confidence intervals (CI)  = 0.59–0.97]. Further stepwise regression analysis suggested that rs999885 was an independently protective factor for the prognosis of HCC in the final model (additive model: adjusted HR  = 0.72, 95% CI  = 0.56–0.91, P = 0.007). CONCLUSIONS: These findings indicate that the A to G base change of rs999885 may provide a protective effect on the prognosis of intermediate or advanced HCC in Chinese.
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spelling pubmed-38857102014-01-10 A Genetic Variant in the Promoter Region of miR-106b-25 Cluster Predict Clinical Outcome of HBV-Related Hepatocellular Carcinoma in Chinese Qi, Fuzhen Huang, Mingde Pan, Yun Liu, Yao Liu, Jibin Wen, Juan Xie, Kaipeng Shen, Hongbing Ma, Hongxia Miao, Yi Hu, Zhibin PLoS One Research Article BACKGROUND: MiR-106b-25 cluster, hosted in intron 13 of MCM7, may play integral roles in diverse processes including immune response, tumorigenesis and progression. A single nucleotide polymorphism (SNP), rs999885, is located in the promoter region of MCM7. Our previous study showed that the A to G base change of rs999885 may provide an increased risk for HCC in HBV persistent carriers by altering the expression of the miR-106b-25 cluster. However, it is unknown whether rs999885 is associated with prognosis of intermediate or advanced HBV-related hepatocellular carcinoma (HCC) patients. METHODS: The SNP, rs999885, was genotyped by using the TaqMan allelic discrimination Assay in 414 intermediate or advanced HCC patients. Log-rank test and Cox proportional hazard models were used for survival analysis. RESULTS: The variant genotypes of rs999885 were associated with a significantly decreased risk of death for intermediate or advanced HCC [additive model: adjusted hazard ratio (HR)  = 0.76,95% confidence intervals (CI)  = 0.59–0.97]. Further stepwise regression analysis suggested that rs999885 was an independently protective factor for the prognosis of HCC in the final model (additive model: adjusted HR  = 0.72, 95% CI  = 0.56–0.91, P = 0.007). CONCLUSIONS: These findings indicate that the A to G base change of rs999885 may provide a protective effect on the prognosis of intermediate or advanced HCC in Chinese. Public Library of Science 2014-01-08 /pmc/articles/PMC3885710/ /pubmed/24416400 http://dx.doi.org/10.1371/journal.pone.0085394 Text en © 2014 Qi et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Qi, Fuzhen
Huang, Mingde
Pan, Yun
Liu, Yao
Liu, Jibin
Wen, Juan
Xie, Kaipeng
Shen, Hongbing
Ma, Hongxia
Miao, Yi
Hu, Zhibin
A Genetic Variant in the Promoter Region of miR-106b-25 Cluster Predict Clinical Outcome of HBV-Related Hepatocellular Carcinoma in Chinese
title A Genetic Variant in the Promoter Region of miR-106b-25 Cluster Predict Clinical Outcome of HBV-Related Hepatocellular Carcinoma in Chinese
title_full A Genetic Variant in the Promoter Region of miR-106b-25 Cluster Predict Clinical Outcome of HBV-Related Hepatocellular Carcinoma in Chinese
title_fullStr A Genetic Variant in the Promoter Region of miR-106b-25 Cluster Predict Clinical Outcome of HBV-Related Hepatocellular Carcinoma in Chinese
title_full_unstemmed A Genetic Variant in the Promoter Region of miR-106b-25 Cluster Predict Clinical Outcome of HBV-Related Hepatocellular Carcinoma in Chinese
title_short A Genetic Variant in the Promoter Region of miR-106b-25 Cluster Predict Clinical Outcome of HBV-Related Hepatocellular Carcinoma in Chinese
title_sort genetic variant in the promoter region of mir-106b-25 cluster predict clinical outcome of hbv-related hepatocellular carcinoma in chinese
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3885710/
https://www.ncbi.nlm.nih.gov/pubmed/24416400
http://dx.doi.org/10.1371/journal.pone.0085394
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