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MiR-26a Promotes Ovarian Cancer Proliferation and Tumorigenesis
MicroRNAs (miRNAs) important for posttranscriptional gene expression are involved in the initiation and progression of human cancer. In this study, we reported that miR-26a was over-expressed in human EOC specimens and the expression level of extracellular miR-26a in plasma can distinguish patients...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3899311/ https://www.ncbi.nlm.nih.gov/pubmed/24466274 http://dx.doi.org/10.1371/journal.pone.0086871 |
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author | Shen, Wenjing Song, Min Liu, Jie Qiu, Guangrong Li, Tianren Hu, Yanjie Liu, Hongbo |
author_facet | Shen, Wenjing Song, Min Liu, Jie Qiu, Guangrong Li, Tianren Hu, Yanjie Liu, Hongbo |
author_sort | Shen, Wenjing |
collection | PubMed |
description | MicroRNAs (miRNAs) important for posttranscriptional gene expression are involved in the initiation and progression of human cancer. In this study, we reported that miR-26a was over-expressed in human EOC specimens and the expression level of extracellular miR-26a in plasma can distinguish patients from healthy controls in EOC. Ectopic expression of miR-26a in ovarian cancer (OC) cells increased cell proliferation and clonal formation. This growth promoting effect of OC cell growth was mediated by miR-26a inhibition of the posttranscription of ER-α. Furthermore, inhibition of miR-26a suppressed the tumor formation generated by injecting OC cells in nude mice. Our results suggest that aberrantly expressed miR-26a may contribute to OC development. |
format | Online Article Text |
id | pubmed-3899311 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-38993112014-01-24 MiR-26a Promotes Ovarian Cancer Proliferation and Tumorigenesis Shen, Wenjing Song, Min Liu, Jie Qiu, Guangrong Li, Tianren Hu, Yanjie Liu, Hongbo PLoS One Research Article MicroRNAs (miRNAs) important for posttranscriptional gene expression are involved in the initiation and progression of human cancer. In this study, we reported that miR-26a was over-expressed in human EOC specimens and the expression level of extracellular miR-26a in plasma can distinguish patients from healthy controls in EOC. Ectopic expression of miR-26a in ovarian cancer (OC) cells increased cell proliferation and clonal formation. This growth promoting effect of OC cell growth was mediated by miR-26a inhibition of the posttranscription of ER-α. Furthermore, inhibition of miR-26a suppressed the tumor formation generated by injecting OC cells in nude mice. Our results suggest that aberrantly expressed miR-26a may contribute to OC development. Public Library of Science 2014-01-22 /pmc/articles/PMC3899311/ /pubmed/24466274 http://dx.doi.org/10.1371/journal.pone.0086871 Text en © 2014 Shen 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 Shen, Wenjing Song, Min Liu, Jie Qiu, Guangrong Li, Tianren Hu, Yanjie Liu, Hongbo MiR-26a Promotes Ovarian Cancer Proliferation and Tumorigenesis |
title |
MiR-26a Promotes Ovarian Cancer Proliferation and Tumorigenesis |
title_full |
MiR-26a Promotes Ovarian Cancer Proliferation and Tumorigenesis |
title_fullStr |
MiR-26a Promotes Ovarian Cancer Proliferation and Tumorigenesis |
title_full_unstemmed |
MiR-26a Promotes Ovarian Cancer Proliferation and Tumorigenesis |
title_short |
MiR-26a Promotes Ovarian Cancer Proliferation and Tumorigenesis |
title_sort | mir-26a promotes ovarian cancer proliferation and tumorigenesis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3899311/ https://www.ncbi.nlm.nih.gov/pubmed/24466274 http://dx.doi.org/10.1371/journal.pone.0086871 |
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