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RABEX-5 plays an oncogenic role in breast cancer by activating MMP-9 pathway
BACKGROUND: RABEX-5, a guanine nucleotide exchange factor (GEF) for RAB-5, plays an important role in cell mobility and altered expression associated with tumor metastasis. This study aimed to investigate the role of RABEX-5 in proliferation and metastasis of breast cancer in vitro and ex vivo. METH...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3751292/ https://www.ncbi.nlm.nih.gov/pubmed/23941575 http://dx.doi.org/10.1186/1756-9966-32-52 |
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author | Zhang, Xiang Min, Jie Wang, Yingjian Li, Yan Li, Hongzhong Liu, Qiang Liang, Xinjie Mu, Peng Li, Hongyuan |
author_facet | Zhang, Xiang Min, Jie Wang, Yingjian Li, Yan Li, Hongzhong Liu, Qiang Liang, Xinjie Mu, Peng Li, Hongyuan |
author_sort | Zhang, Xiang |
collection | PubMed |
description | BACKGROUND: RABEX-5, a guanine nucleotide exchange factor (GEF) for RAB-5, plays an important role in cell mobility and altered expression associated with tumor metastasis. This study aimed to investigate the role of RABEX-5 in proliferation and metastasis of breast cancer in vitro and ex vivo. METHODS: RABEX-5 expression was examined in breast cancer, benign tumor and normal breast tissues by immunohistochemistry and western blot. Two stable cell lines were established, the MCF-7/NC negative control cell line and the MCF-7/KD cell line, which stably expressed an RNA interference (RNAi) construct that induced downregulation of RABEX-5 expression. These cell lines were utilized to evaluate the role of RABEX-5 in cell proliferation and migration in vitro and tumorigenicity in vivo. The possible role of RABEX-5 in the regulation of matrix metallopeptidase 9 (MMP-9) was evaluated using western blot and real-time PCR. RESULTS: RABEX-5 expression was found to be significantly higher in breast cancer tissues compared with benign tumor and normal breast tissues. High levels of RABEX-5 expression were associated with axillary lymph node metastasis. In addition, RABEX-5 silencing significantly reduced cancer cell proliferation, colony formation and migration ability in vitro and inhibited tumor growth in vivo. RABEX −5 knockdown also attenuated the migration of breast cancer cells via modulation of MMP-9 transcriptional activity. CONCLUSIONS: Our results indicate that RABEX-5 plays an oncogenic role in breast cancer by modulating the proliferation and metastasis potential of breast cancer cells. Thus, RABEX-5 is a promising prognostic indicator for patients with breast cancer. |
format | Online Article Text |
id | pubmed-3751292 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-37512922013-08-24 RABEX-5 plays an oncogenic role in breast cancer by activating MMP-9 pathway Zhang, Xiang Min, Jie Wang, Yingjian Li, Yan Li, Hongzhong Liu, Qiang Liang, Xinjie Mu, Peng Li, Hongyuan J Exp Clin Cancer Res Research BACKGROUND: RABEX-5, a guanine nucleotide exchange factor (GEF) for RAB-5, plays an important role in cell mobility and altered expression associated with tumor metastasis. This study aimed to investigate the role of RABEX-5 in proliferation and metastasis of breast cancer in vitro and ex vivo. METHODS: RABEX-5 expression was examined in breast cancer, benign tumor and normal breast tissues by immunohistochemistry and western blot. Two stable cell lines were established, the MCF-7/NC negative control cell line and the MCF-7/KD cell line, which stably expressed an RNA interference (RNAi) construct that induced downregulation of RABEX-5 expression. These cell lines were utilized to evaluate the role of RABEX-5 in cell proliferation and migration in vitro and tumorigenicity in vivo. The possible role of RABEX-5 in the regulation of matrix metallopeptidase 9 (MMP-9) was evaluated using western blot and real-time PCR. RESULTS: RABEX-5 expression was found to be significantly higher in breast cancer tissues compared with benign tumor and normal breast tissues. High levels of RABEX-5 expression were associated with axillary lymph node metastasis. In addition, RABEX-5 silencing significantly reduced cancer cell proliferation, colony formation and migration ability in vitro and inhibited tumor growth in vivo. RABEX −5 knockdown also attenuated the migration of breast cancer cells via modulation of MMP-9 transcriptional activity. CONCLUSIONS: Our results indicate that RABEX-5 plays an oncogenic role in breast cancer by modulating the proliferation and metastasis potential of breast cancer cells. Thus, RABEX-5 is a promising prognostic indicator for patients with breast cancer. BioMed Central 2013-08-13 /pmc/articles/PMC3751292/ /pubmed/23941575 http://dx.doi.org/10.1186/1756-9966-32-52 Text en Copyright © 2013 Zhang et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Zhang, Xiang Min, Jie Wang, Yingjian Li, Yan Li, Hongzhong Liu, Qiang Liang, Xinjie Mu, Peng Li, Hongyuan RABEX-5 plays an oncogenic role in breast cancer by activating MMP-9 pathway |
title | RABEX-5 plays an oncogenic role in breast cancer by activating MMP-9 pathway |
title_full | RABEX-5 plays an oncogenic role in breast cancer by activating MMP-9 pathway |
title_fullStr | RABEX-5 plays an oncogenic role in breast cancer by activating MMP-9 pathway |
title_full_unstemmed | RABEX-5 plays an oncogenic role in breast cancer by activating MMP-9 pathway |
title_short | RABEX-5 plays an oncogenic role in breast cancer by activating MMP-9 pathway |
title_sort | rabex-5 plays an oncogenic role in breast cancer by activating mmp-9 pathway |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3751292/ https://www.ncbi.nlm.nih.gov/pubmed/23941575 http://dx.doi.org/10.1186/1756-9966-32-52 |
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