Cargando…

MicroRNA-185 inhibits proliferation by targeting c-Met in human breast cancer cells

MicroRNAs (miRNAs) are a group of small non-coding RNA molecules that have been shown to regulate the expression of genes involved in tumorigenesis. The relevance of miRNAs in the development, progression and prognosis of human breast cancer is not fully understood. miR-185 has been demonstrated to...

Descripción completa

Detalles Bibliográficos
Autores principales: FU, PEIFEN, DU, FEIYA, YAO, MINYA, LV, KEZHEN, LIU, YU
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4217781/
https://www.ncbi.nlm.nih.gov/pubmed/25371748
http://dx.doi.org/10.3892/etm.2014.1999
_version_ 1782342446788640768
author FU, PEIFEN
DU, FEIYA
YAO, MINYA
LV, KEZHEN
LIU, YU
author_facet FU, PEIFEN
DU, FEIYA
YAO, MINYA
LV, KEZHEN
LIU, YU
author_sort FU, PEIFEN
collection PubMed
description MicroRNAs (miRNAs) are a group of small non-coding RNA molecules that have been shown to regulate the expression of genes involved in tumorigenesis. The relevance of miRNAs in the development, progression and prognosis of human breast cancer is not fully understood. miR-185 has been demonstrated to be involved in the pathogenesis of several types of cancers; however, its role in breast cancer has not yet been elucidated. In the present study, the expression of miR-185 was analyzed by quantitative polymerase chain reaction. In addition, an MTT assay and flow cytometry were used to determine the rates of cell proliferation and apoptosis. Protein expression was analyzed by western blotting and the target gene was confirmed using a luciferase reporter assay. The expression of miR-185 was found to be downregulated in the breast cancer tissues. The MTT assay revealed that overexpression of miR-185 inhibited the proliferation of MDF7 and SKBR3 cells. Furthermore, flow cytometric analysis demonstrated that increased expression levels of miR-185 promoted the apoptosis of breast cancer cells. In addition, c-Met expression was demonstrated to be significantly upregulated in breast cancer tissues and cells, and the c-Met gene was identified to be a target of miR-185. Therefore, the results demonstrated that miR-185 inhibited the proliferation of breast cancer cells by regulating the expression of c-Met, indicating its potential as a therapeutic target for breast cancer.
format Online
Article
Text
id pubmed-4217781
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher D.A. Spandidos
record_format MEDLINE/PubMed
spelling pubmed-42177812014-11-04 MicroRNA-185 inhibits proliferation by targeting c-Met in human breast cancer cells FU, PEIFEN DU, FEIYA YAO, MINYA LV, KEZHEN LIU, YU Exp Ther Med Articles MicroRNAs (miRNAs) are a group of small non-coding RNA molecules that have been shown to regulate the expression of genes involved in tumorigenesis. The relevance of miRNAs in the development, progression and prognosis of human breast cancer is not fully understood. miR-185 has been demonstrated to be involved in the pathogenesis of several types of cancers; however, its role in breast cancer has not yet been elucidated. In the present study, the expression of miR-185 was analyzed by quantitative polymerase chain reaction. In addition, an MTT assay and flow cytometry were used to determine the rates of cell proliferation and apoptosis. Protein expression was analyzed by western blotting and the target gene was confirmed using a luciferase reporter assay. The expression of miR-185 was found to be downregulated in the breast cancer tissues. The MTT assay revealed that overexpression of miR-185 inhibited the proliferation of MDF7 and SKBR3 cells. Furthermore, flow cytometric analysis demonstrated that increased expression levels of miR-185 promoted the apoptosis of breast cancer cells. In addition, c-Met expression was demonstrated to be significantly upregulated in breast cancer tissues and cells, and the c-Met gene was identified to be a target of miR-185. Therefore, the results demonstrated that miR-185 inhibited the proliferation of breast cancer cells by regulating the expression of c-Met, indicating its potential as a therapeutic target for breast cancer. D.A. Spandidos 2014-12 2014-09-30 /pmc/articles/PMC4217781/ /pubmed/25371748 http://dx.doi.org/10.3892/etm.2014.1999 Text en Copyright © 2014, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
FU, PEIFEN
DU, FEIYA
YAO, MINYA
LV, KEZHEN
LIU, YU
MicroRNA-185 inhibits proliferation by targeting c-Met in human breast cancer cells
title MicroRNA-185 inhibits proliferation by targeting c-Met in human breast cancer cells
title_full MicroRNA-185 inhibits proliferation by targeting c-Met in human breast cancer cells
title_fullStr MicroRNA-185 inhibits proliferation by targeting c-Met in human breast cancer cells
title_full_unstemmed MicroRNA-185 inhibits proliferation by targeting c-Met in human breast cancer cells
title_short MicroRNA-185 inhibits proliferation by targeting c-Met in human breast cancer cells
title_sort microrna-185 inhibits proliferation by targeting c-met in human breast cancer cells
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4217781/
https://www.ncbi.nlm.nih.gov/pubmed/25371748
http://dx.doi.org/10.3892/etm.2014.1999
work_keys_str_mv AT fupeifen microrna185inhibitsproliferationbytargetingcmetinhumanbreastcancercells
AT dufeiya microrna185inhibitsproliferationbytargetingcmetinhumanbreastcancercells
AT yaominya microrna185inhibitsproliferationbytargetingcmetinhumanbreastcancercells
AT lvkezhen microrna185inhibitsproliferationbytargetingcmetinhumanbreastcancercells
AT liuyu microrna185inhibitsproliferationbytargetingcmetinhumanbreastcancercells