Cargando…
MicroRNA-22 Suppresses Breast Cancer Cell Growth and Increases Paclitaxel Sensitivity by Targeting NRAS
In recent study, microRNAs have various important functions in diverse biological processes and progression of cancer. In human breast cancer, microRNA-22 has been reported to be downregulated. However, molecular mechanism of microRNA-22 in breast cancer progression and chemosensitivity has not been...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259065/ https://www.ncbi.nlm.nih.gov/pubmed/30384806 http://dx.doi.org/10.1177/1533033818809997 |
_version_ | 1783374602779492352 |
---|---|
author | Song, Ying-kui Wang, Yang Wen, Yi-yang Zhao, Pei Bian, Zhi-jie |
author_facet | Song, Ying-kui Wang, Yang Wen, Yi-yang Zhao, Pei Bian, Zhi-jie |
author_sort | Song, Ying-kui |
collection | PubMed |
description | In recent study, microRNAs have various important functions in diverse biological processes and progression of cancer. In human breast cancer, microRNA-22 has been reported to be downregulated. However, molecular mechanism of microRNA-22 in breast cancer progression and chemosensitivity has not been well studied. In our study, these results demonstrated that microRNA-22 expression levels were significantly reduced in 40 pairs of human breast cancer tissues when compared to normal tissues. Enforced expression of microRNA-22 inhibited activity of cell proliferation and cell migration in breast cancer cells. Furthermore, microRNA-22 targeted NRAS proto-oncogene, GTPase (NRAS) in breast cancer cells. The expression levels of NRAS in human clinical specimens were higher in breast cancer tissues when compared to normal tissues. Moreover, microRNA-22 sensitized breast cancer cells to paclitaxel by regulation of NRAS. Our results then demonstrated that microRNA-22 functioned as a tumor suppressor microRNA and indicated potential application for the diagnosis and treatment of cancer in the future. |
format | Online Article Text |
id | pubmed-6259065 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-62590652018-11-30 MicroRNA-22 Suppresses Breast Cancer Cell Growth and Increases Paclitaxel Sensitivity by Targeting NRAS Song, Ying-kui Wang, Yang Wen, Yi-yang Zhao, Pei Bian, Zhi-jie Technol Cancer Res Treat Original Article In recent study, microRNAs have various important functions in diverse biological processes and progression of cancer. In human breast cancer, microRNA-22 has been reported to be downregulated. However, molecular mechanism of microRNA-22 in breast cancer progression and chemosensitivity has not been well studied. In our study, these results demonstrated that microRNA-22 expression levels were significantly reduced in 40 pairs of human breast cancer tissues when compared to normal tissues. Enforced expression of microRNA-22 inhibited activity of cell proliferation and cell migration in breast cancer cells. Furthermore, microRNA-22 targeted NRAS proto-oncogene, GTPase (NRAS) in breast cancer cells. The expression levels of NRAS in human clinical specimens were higher in breast cancer tissues when compared to normal tissues. Moreover, microRNA-22 sensitized breast cancer cells to paclitaxel by regulation of NRAS. Our results then demonstrated that microRNA-22 functioned as a tumor suppressor microRNA and indicated potential application for the diagnosis and treatment of cancer in the future. SAGE Publications 2018-11-01 /pmc/articles/PMC6259065/ /pubmed/30384806 http://dx.doi.org/10.1177/1533033818809997 Text en © The Author(s) 2018 http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Article Song, Ying-kui Wang, Yang Wen, Yi-yang Zhao, Pei Bian, Zhi-jie MicroRNA-22 Suppresses Breast Cancer Cell Growth and Increases Paclitaxel Sensitivity by Targeting NRAS |
title | MicroRNA-22 Suppresses Breast Cancer Cell Growth and Increases Paclitaxel
Sensitivity by Targeting NRAS |
title_full | MicroRNA-22 Suppresses Breast Cancer Cell Growth and Increases Paclitaxel
Sensitivity by Targeting NRAS |
title_fullStr | MicroRNA-22 Suppresses Breast Cancer Cell Growth and Increases Paclitaxel
Sensitivity by Targeting NRAS |
title_full_unstemmed | MicroRNA-22 Suppresses Breast Cancer Cell Growth and Increases Paclitaxel
Sensitivity by Targeting NRAS |
title_short | MicroRNA-22 Suppresses Breast Cancer Cell Growth and Increases Paclitaxel
Sensitivity by Targeting NRAS |
title_sort | microrna-22 suppresses breast cancer cell growth and increases paclitaxel
sensitivity by targeting nras |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259065/ https://www.ncbi.nlm.nih.gov/pubmed/30384806 http://dx.doi.org/10.1177/1533033818809997 |
work_keys_str_mv | AT songyingkui microrna22suppressesbreastcancercellgrowthandincreasespaclitaxelsensitivitybytargetingnras AT wangyang microrna22suppressesbreastcancercellgrowthandincreasespaclitaxelsensitivitybytargetingnras AT wenyiyang microrna22suppressesbreastcancercellgrowthandincreasespaclitaxelsensitivitybytargetingnras AT zhaopei microrna22suppressesbreastcancercellgrowthandincreasespaclitaxelsensitivitybytargetingnras AT bianzhijie microrna22suppressesbreastcancercellgrowthandincreasespaclitaxelsensitivitybytargetingnras |