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3′UTR polymorphisms of carbonic anhydrase IX determine the miR-34a targeting efficiency and prognosis of hepatocellular carcinoma

Carbonic anhydrase IX (CA9) expression level has been considered as a poor prognostic factor in hepatocellular carcinoma (HCC) patients. However, the judging criteria of CA9 level is hard to define for potential clinical applications. Unlike CA9 expression level, CA9 polymorphism is poorly documente...

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Autores principales: Hua, Kuo-Tai, Liu, Yu-Fan, Hsu, Chia-Lang, Cheng, Tsu-Yao, Yang, Ching-Yao, Chang, Jeng-Shou, Lee, Wei-Jiunn, Hsiao, Michael, Juan, Hsueh-Fen, Chien, Ming-Hsien, Yang, Shun-Fa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5493636/
https://www.ncbi.nlm.nih.gov/pubmed/28667334
http://dx.doi.org/10.1038/s41598-017-04732-3
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author Hua, Kuo-Tai
Liu, Yu-Fan
Hsu, Chia-Lang
Cheng, Tsu-Yao
Yang, Ching-Yao
Chang, Jeng-Shou
Lee, Wei-Jiunn
Hsiao, Michael
Juan, Hsueh-Fen
Chien, Ming-Hsien
Yang, Shun-Fa
author_facet Hua, Kuo-Tai
Liu, Yu-Fan
Hsu, Chia-Lang
Cheng, Tsu-Yao
Yang, Ching-Yao
Chang, Jeng-Shou
Lee, Wei-Jiunn
Hsiao, Michael
Juan, Hsueh-Fen
Chien, Ming-Hsien
Yang, Shun-Fa
author_sort Hua, Kuo-Tai
collection PubMed
description Carbonic anhydrase IX (CA9) expression level has been considered as a poor prognostic factor in hepatocellular carcinoma (HCC) patients. However, the judging criteria of CA9 level is hard to define for potential clinical applications. Unlike CA9 expression level, CA9 polymorphism is poorly documented in HCC. Here, we found that people carry A allele at CA9 rs1048638, a 3′UTR SNP, has higher risk of HCC. rs1048638-CA correlates with advanced stages, larger tumor sizes, more vascular invasion, and shorter survival of HCC patients. A allele at CA9 rs1048638 impairs miR-34a, a tumor suppressor miRNA in HCC, binding to CA9 3′UTR and desensitizes CA9 mRNA to miR-34a-dependent RNA degradation. CA9 expression levels were also correlated with miR-34a levels and rs1048638 genotypes in HCC patients. rs1048638 influences HCC risk and progression through effects on miR-34a-targeted CA9 expression in HCC. In conclusion, genetic variations of the CA9 3′UTR play important roles in regulating CA9 expression and cancer progression, which is a novel determinant and target for HCC metastasis and prognosis.
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spelling pubmed-54936362017-07-05 3′UTR polymorphisms of carbonic anhydrase IX determine the miR-34a targeting efficiency and prognosis of hepatocellular carcinoma Hua, Kuo-Tai Liu, Yu-Fan Hsu, Chia-Lang Cheng, Tsu-Yao Yang, Ching-Yao Chang, Jeng-Shou Lee, Wei-Jiunn Hsiao, Michael Juan, Hsueh-Fen Chien, Ming-Hsien Yang, Shun-Fa Sci Rep Article Carbonic anhydrase IX (CA9) expression level has been considered as a poor prognostic factor in hepatocellular carcinoma (HCC) patients. However, the judging criteria of CA9 level is hard to define for potential clinical applications. Unlike CA9 expression level, CA9 polymorphism is poorly documented in HCC. Here, we found that people carry A allele at CA9 rs1048638, a 3′UTR SNP, has higher risk of HCC. rs1048638-CA correlates with advanced stages, larger tumor sizes, more vascular invasion, and shorter survival of HCC patients. A allele at CA9 rs1048638 impairs miR-34a, a tumor suppressor miRNA in HCC, binding to CA9 3′UTR and desensitizes CA9 mRNA to miR-34a-dependent RNA degradation. CA9 expression levels were also correlated with miR-34a levels and rs1048638 genotypes in HCC patients. rs1048638 influences HCC risk and progression through effects on miR-34a-targeted CA9 expression in HCC. In conclusion, genetic variations of the CA9 3′UTR play important roles in regulating CA9 expression and cancer progression, which is a novel determinant and target for HCC metastasis and prognosis. Nature Publishing Group UK 2017-06-30 /pmc/articles/PMC5493636/ /pubmed/28667334 http://dx.doi.org/10.1038/s41598-017-04732-3 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Hua, Kuo-Tai
Liu, Yu-Fan
Hsu, Chia-Lang
Cheng, Tsu-Yao
Yang, Ching-Yao
Chang, Jeng-Shou
Lee, Wei-Jiunn
Hsiao, Michael
Juan, Hsueh-Fen
Chien, Ming-Hsien
Yang, Shun-Fa
3′UTR polymorphisms of carbonic anhydrase IX determine the miR-34a targeting efficiency and prognosis of hepatocellular carcinoma
title 3′UTR polymorphisms of carbonic anhydrase IX determine the miR-34a targeting efficiency and prognosis of hepatocellular carcinoma
title_full 3′UTR polymorphisms of carbonic anhydrase IX determine the miR-34a targeting efficiency and prognosis of hepatocellular carcinoma
title_fullStr 3′UTR polymorphisms of carbonic anhydrase IX determine the miR-34a targeting efficiency and prognosis of hepatocellular carcinoma
title_full_unstemmed 3′UTR polymorphisms of carbonic anhydrase IX determine the miR-34a targeting efficiency and prognosis of hepatocellular carcinoma
title_short 3′UTR polymorphisms of carbonic anhydrase IX determine the miR-34a targeting efficiency and prognosis of hepatocellular carcinoma
title_sort 3′utr polymorphisms of carbonic anhydrase ix determine the mir-34a targeting efficiency and prognosis of hepatocellular carcinoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5493636/
https://www.ncbi.nlm.nih.gov/pubmed/28667334
http://dx.doi.org/10.1038/s41598-017-04732-3
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