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A Genetic Variant in Primary miR-378 Is Associated with Risk and Prognosis of Hepatocellular Carcinoma in a Chinese Population

BACKGROUND: MiR-378 has been reported to be related to cell survival, tumor growth and angiogenesis and may participate in hepatocellular carcinoma (HCC) development and prognosis. Genetic variants in primary miR-378 (pri-miR-378) may impact miR-378 expression and contribute to HCC risk and survival...

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Autores principales: An, Jiaze, Liu, Jibin, Liu, Li, Liu, Yao, Pan, Yun, Huang, Mingde, Qi, Fuzhen, Wen, Juan, Xie, Kaipeng, Ma, Hongxia, Shen, Hongbing, 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/PMC3994025/
https://www.ncbi.nlm.nih.gov/pubmed/24751683
http://dx.doi.org/10.1371/journal.pone.0093707
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author An, Jiaze
Liu, Jibin
Liu, Li
Liu, Yao
Pan, Yun
Huang, Mingde
Qi, Fuzhen
Wen, Juan
Xie, Kaipeng
Ma, Hongxia
Shen, Hongbing
Hu, Zhibin
author_facet An, Jiaze
Liu, Jibin
Liu, Li
Liu, Yao
Pan, Yun
Huang, Mingde
Qi, Fuzhen
Wen, Juan
Xie, Kaipeng
Ma, Hongxia
Shen, Hongbing
Hu, Zhibin
author_sort An, Jiaze
collection PubMed
description BACKGROUND: MiR-378 has been reported to be related to cell survival, tumor growth and angiogenesis and may participate in hepatocellular carcinoma (HCC) development and prognosis. Genetic variants in primary miR-378 (pri-miR-378) may impact miR-378 expression and contribute to HCC risk and survival. This study aimed to assess the associations between a genetic variant in primary miR-378 and HCC susceptibility and prognosis. METHODS: We conducted a case-control study to analyze the association of rs1076064 in pri-miR-378 with hepatocellular carcinoma risk in 1300 HCC patients with positive hepatitis B virus (HBV) and 1344 HBV carriers. Then, we evaluated the correlation between the polymorphism and hepatocellular carcinoma prognosis in 331 HCC patients at either intermediate or advanced stage without surgical treatment. RESULTS: The variant genotypes of rs1076064 were associated with a decreased HCC risk in HBV carriers [Adjusted odds ratio (OR) = 0.90, 95% confidence intervals (CI) = 0.81–1.00, P = 0.047]. Moreover, HCC patients with the variant genotypes were associated with a better survival [Adjusted hazard ratio (HR) = 0.70, 95% CIs = 0.59–0.83, P<0.0001 in an additive genetic model]. The reporter gene assay showed that the variant G allele of rs1076064 exerted higher promoter activity than the A allele. CONCLUSIONS: These findings indicate that rs1076064 may be a biomarker for HCC susceptibility and prognosis through altering pri-miR-378 transcription.
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spelling pubmed-39940252014-04-25 A Genetic Variant in Primary miR-378 Is Associated with Risk and Prognosis of Hepatocellular Carcinoma in a Chinese Population An, Jiaze Liu, Jibin Liu, Li Liu, Yao Pan, Yun Huang, Mingde Qi, Fuzhen Wen, Juan Xie, Kaipeng Ma, Hongxia Shen, Hongbing Hu, Zhibin PLoS One Research Article BACKGROUND: MiR-378 has been reported to be related to cell survival, tumor growth and angiogenesis and may participate in hepatocellular carcinoma (HCC) development and prognosis. Genetic variants in primary miR-378 (pri-miR-378) may impact miR-378 expression and contribute to HCC risk and survival. This study aimed to assess the associations between a genetic variant in primary miR-378 and HCC susceptibility and prognosis. METHODS: We conducted a case-control study to analyze the association of rs1076064 in pri-miR-378 with hepatocellular carcinoma risk in 1300 HCC patients with positive hepatitis B virus (HBV) and 1344 HBV carriers. Then, we evaluated the correlation between the polymorphism and hepatocellular carcinoma prognosis in 331 HCC patients at either intermediate or advanced stage without surgical treatment. RESULTS: The variant genotypes of rs1076064 were associated with a decreased HCC risk in HBV carriers [Adjusted odds ratio (OR) = 0.90, 95% confidence intervals (CI) = 0.81–1.00, P = 0.047]. Moreover, HCC patients with the variant genotypes were associated with a better survival [Adjusted hazard ratio (HR) = 0.70, 95% CIs = 0.59–0.83, P<0.0001 in an additive genetic model]. The reporter gene assay showed that the variant G allele of rs1076064 exerted higher promoter activity than the A allele. CONCLUSIONS: These findings indicate that rs1076064 may be a biomarker for HCC susceptibility and prognosis through altering pri-miR-378 transcription. Public Library of Science 2014-04-21 /pmc/articles/PMC3994025/ /pubmed/24751683 http://dx.doi.org/10.1371/journal.pone.0093707 Text en © 2014 An 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
An, Jiaze
Liu, Jibin
Liu, Li
Liu, Yao
Pan, Yun
Huang, Mingde
Qi, Fuzhen
Wen, Juan
Xie, Kaipeng
Ma, Hongxia
Shen, Hongbing
Hu, Zhibin
A Genetic Variant in Primary miR-378 Is Associated with Risk and Prognosis of Hepatocellular Carcinoma in a Chinese Population
title A Genetic Variant in Primary miR-378 Is Associated with Risk and Prognosis of Hepatocellular Carcinoma in a Chinese Population
title_full A Genetic Variant in Primary miR-378 Is Associated with Risk and Prognosis of Hepatocellular Carcinoma in a Chinese Population
title_fullStr A Genetic Variant in Primary miR-378 Is Associated with Risk and Prognosis of Hepatocellular Carcinoma in a Chinese Population
title_full_unstemmed A Genetic Variant in Primary miR-378 Is Associated with Risk and Prognosis of Hepatocellular Carcinoma in a Chinese Population
title_short A Genetic Variant in Primary miR-378 Is Associated with Risk and Prognosis of Hepatocellular Carcinoma in a Chinese Population
title_sort genetic variant in primary mir-378 is associated with risk and prognosis of hepatocellular carcinoma in a chinese population
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3994025/
https://www.ncbi.nlm.nih.gov/pubmed/24751683
http://dx.doi.org/10.1371/journal.pone.0093707
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