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miR‐206 inhibits the growth of hepatocellular carcinoma cells via targeting CDK9
miR‐206 plays an important role in regulating the growth of multiple cancer cells. Cyclin‐dependent kinase 9 (CDK9) stimulates the production of abundant prosurvival proteins, leading to impaired apoptosis of cancer cells. However, it is unknown whether CDK9 is involved in the miR‐206‐mediated growt...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5633544/ https://www.ncbi.nlm.nih.gov/pubmed/28940993 http://dx.doi.org/10.1002/cam4.1188 |
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author | Pang, Chi Huang, Gang Luo, Kaili Dong, Yuying He, Fengtian Du, Guankui Xiao, Man Cai, Wangwei |
author_facet | Pang, Chi Huang, Gang Luo, Kaili Dong, Yuying He, Fengtian Du, Guankui Xiao, Man Cai, Wangwei |
author_sort | Pang, Chi |
collection | PubMed |
description | miR‐206 plays an important role in regulating the growth of multiple cancer cells. Cyclin‐dependent kinase 9 (CDK9) stimulates the production of abundant prosurvival proteins, leading to impaired apoptosis of cancer cells. However, it is unknown whether CDK9 is involved in the miR‐206‐mediated growth suppression of hepatocellular carcinoma (HCC) cells. In this study, we found that the expression level of miR‐206 was significantly lower in HCC cell lines than that in normal hepatic cell line (L02). Meanwhile, CDK9 was upregulated in HCC cell lines. Moreover, miR‐206 downregulated CDK9 in HCC cells via directly binding to its mRNA 3′ UTR, which resulted in a decrease of RNA PolII Ser2 phosphorylation and Mcl‐1 level. Additionally, miR‐206 suppressed the cell proliferation, and induced cell cycle arrest and apoptosis. Similarly, silence or inhibition of CDK9 also repressed the cell proliferation, and induced cell cycle arrest and apoptosis. Taken together, the results demonstrated that miR‐206 inhibited the growth of HCC cells through targeting CDK9, suggesting that the miR‐206‐CDK9 pathway may be a novel target for the treatment of HCC. |
format | Online Article Text |
id | pubmed-5633544 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-56335442017-10-17 miR‐206 inhibits the growth of hepatocellular carcinoma cells via targeting CDK9 Pang, Chi Huang, Gang Luo, Kaili Dong, Yuying He, Fengtian Du, Guankui Xiao, Man Cai, Wangwei Cancer Med Cancer Biology miR‐206 plays an important role in regulating the growth of multiple cancer cells. Cyclin‐dependent kinase 9 (CDK9) stimulates the production of abundant prosurvival proteins, leading to impaired apoptosis of cancer cells. However, it is unknown whether CDK9 is involved in the miR‐206‐mediated growth suppression of hepatocellular carcinoma (HCC) cells. In this study, we found that the expression level of miR‐206 was significantly lower in HCC cell lines than that in normal hepatic cell line (L02). Meanwhile, CDK9 was upregulated in HCC cell lines. Moreover, miR‐206 downregulated CDK9 in HCC cells via directly binding to its mRNA 3′ UTR, which resulted in a decrease of RNA PolII Ser2 phosphorylation and Mcl‐1 level. Additionally, miR‐206 suppressed the cell proliferation, and induced cell cycle arrest and apoptosis. Similarly, silence or inhibition of CDK9 also repressed the cell proliferation, and induced cell cycle arrest and apoptosis. Taken together, the results demonstrated that miR‐206 inhibited the growth of HCC cells through targeting CDK9, suggesting that the miR‐206‐CDK9 pathway may be a novel target for the treatment of HCC. John Wiley and Sons Inc. 2017-09-21 /pmc/articles/PMC5633544/ /pubmed/28940993 http://dx.doi.org/10.1002/cam4.1188 Text en © 2017 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Cancer Biology Pang, Chi Huang, Gang Luo, Kaili Dong, Yuying He, Fengtian Du, Guankui Xiao, Man Cai, Wangwei miR‐206 inhibits the growth of hepatocellular carcinoma cells via targeting CDK9 |
title | miR‐206 inhibits the growth of hepatocellular carcinoma cells via targeting CDK9 |
title_full | miR‐206 inhibits the growth of hepatocellular carcinoma cells via targeting CDK9 |
title_fullStr | miR‐206 inhibits the growth of hepatocellular carcinoma cells via targeting CDK9 |
title_full_unstemmed | miR‐206 inhibits the growth of hepatocellular carcinoma cells via targeting CDK9 |
title_short | miR‐206 inhibits the growth of hepatocellular carcinoma cells via targeting CDK9 |
title_sort | mir‐206 inhibits the growth of hepatocellular carcinoma cells via targeting cdk9 |
topic | Cancer Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5633544/ https://www.ncbi.nlm.nih.gov/pubmed/28940993 http://dx.doi.org/10.1002/cam4.1188 |
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