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High Expression of MicroRNA-196a is Associated with Progression of Hepatocellular Carcinoma in Younger Patients
MicroRNAs are small RNAs involved in various biological processes and cancer metastasis. miR-196a was associated with aggressive behaviors in several cancers. The role of miR-196a in hepatocellular carcinoma (HCC) metastasis remains unknown. This study aimed to examine the role of miR-196a in HCC pr...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6826650/ https://www.ncbi.nlm.nih.gov/pubmed/31614906 http://dx.doi.org/10.3390/cancers11101549 |
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author | Wang, Shen-Yung Chen, Chih-Li Hu, Yu-Chen Chi, Yi Huang, Yen-Hua Su, Chien-Wei Jeng, Wen-Juei Liang, Yuh-Jin Wu, Jaw-Ching |
author_facet | Wang, Shen-Yung Chen, Chih-Li Hu, Yu-Chen Chi, Yi Huang, Yen-Hua Su, Chien-Wei Jeng, Wen-Juei Liang, Yuh-Jin Wu, Jaw-Ching |
author_sort | Wang, Shen-Yung |
collection | PubMed |
description | MicroRNAs are small RNAs involved in various biological processes and cancer metastasis. miR-196a was associated with aggressive behaviors in several cancers. The role of miR-196a in hepatocellular carcinoma (HCC) metastasis remains unknown. This study aimed to examine the role of miR-196a in HCC progression. Expression of miR-196a was measured in 83 human HCC samples. The HCC patients with high miR-196a expression had younger ages, lower albumin levels, higher frequency with alpha-fetoprotein (AFP) levels ≥20 ng/mL, more macrovascular invasion, and non-early stages. Kaplan–Meier analysis showed that high miR-196a expression was associated with lower recurrence-free survival. Knockdown of miR-196a decreased transwell invasiveness, sphere formation, transendothelial invasion, and Slug, Twist, Oct4, and Sox2 expression, suppressed angiogenesis, and reduced sizes of xenotransplants and number of pulmonary metastasis. Down-regulation of miR-196a decreased Runx2 and osteopontin (OPN) levels. Knockdown of Runx2 in vitro resulted in comparable phenotypes with miR-196a down-regulation. Restoration of Runx2 in miR-196a-knockdown HCC reverted tumor phenotypes. This study showed that high expression of miR-196a is associated with HCC progression in a subset of younger patients. miR-196a mediates HCC progression via upregulation of Runx2, OPN, epithelial–mesenchymal transition (EMT) regulators, and stemness genes. We proposed that miR-196a can be used as a prognostic marker and a potential therapeutic target. |
format | Online Article Text |
id | pubmed-6826650 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-68266502019-11-18 High Expression of MicroRNA-196a is Associated with Progression of Hepatocellular Carcinoma in Younger Patients Wang, Shen-Yung Chen, Chih-Li Hu, Yu-Chen Chi, Yi Huang, Yen-Hua Su, Chien-Wei Jeng, Wen-Juei Liang, Yuh-Jin Wu, Jaw-Ching Cancers (Basel) Article MicroRNAs are small RNAs involved in various biological processes and cancer metastasis. miR-196a was associated with aggressive behaviors in several cancers. The role of miR-196a in hepatocellular carcinoma (HCC) metastasis remains unknown. This study aimed to examine the role of miR-196a in HCC progression. Expression of miR-196a was measured in 83 human HCC samples. The HCC patients with high miR-196a expression had younger ages, lower albumin levels, higher frequency with alpha-fetoprotein (AFP) levels ≥20 ng/mL, more macrovascular invasion, and non-early stages. Kaplan–Meier analysis showed that high miR-196a expression was associated with lower recurrence-free survival. Knockdown of miR-196a decreased transwell invasiveness, sphere formation, transendothelial invasion, and Slug, Twist, Oct4, and Sox2 expression, suppressed angiogenesis, and reduced sizes of xenotransplants and number of pulmonary metastasis. Down-regulation of miR-196a decreased Runx2 and osteopontin (OPN) levels. Knockdown of Runx2 in vitro resulted in comparable phenotypes with miR-196a down-regulation. Restoration of Runx2 in miR-196a-knockdown HCC reverted tumor phenotypes. This study showed that high expression of miR-196a is associated with HCC progression in a subset of younger patients. miR-196a mediates HCC progression via upregulation of Runx2, OPN, epithelial–mesenchymal transition (EMT) regulators, and stemness genes. We proposed that miR-196a can be used as a prognostic marker and a potential therapeutic target. MDPI 2019-10-13 /pmc/articles/PMC6826650/ /pubmed/31614906 http://dx.doi.org/10.3390/cancers11101549 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Wang, Shen-Yung Chen, Chih-Li Hu, Yu-Chen Chi, Yi Huang, Yen-Hua Su, Chien-Wei Jeng, Wen-Juei Liang, Yuh-Jin Wu, Jaw-Ching High Expression of MicroRNA-196a is Associated with Progression of Hepatocellular Carcinoma in Younger Patients |
title | High Expression of MicroRNA-196a is Associated with Progression of Hepatocellular Carcinoma in Younger Patients |
title_full | High Expression of MicroRNA-196a is Associated with Progression of Hepatocellular Carcinoma in Younger Patients |
title_fullStr | High Expression of MicroRNA-196a is Associated with Progression of Hepatocellular Carcinoma in Younger Patients |
title_full_unstemmed | High Expression of MicroRNA-196a is Associated with Progression of Hepatocellular Carcinoma in Younger Patients |
title_short | High Expression of MicroRNA-196a is Associated with Progression of Hepatocellular Carcinoma in Younger Patients |
title_sort | high expression of microrna-196a is associated with progression of hepatocellular carcinoma in younger patients |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6826650/ https://www.ncbi.nlm.nih.gov/pubmed/31614906 http://dx.doi.org/10.3390/cancers11101549 |
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