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RABEX-5 plays an oncogenic role in breast cancer by activating MMP-9 pathway

Authors :
Yan Li
Xinjie Liang
Ying-jian Wang
Hongyuan Li
Qiang Liu
Hongzhong Li
Xiang Zhang
Peng Mu
Jie Min
Source :
Journal of Experimental & Clinical Cancer Research : CR
Publisher :
Springer Nature

Abstract

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.

Details

Language :
English
ISSN :
17569966
Volume :
32
Issue :
1
Database :
OpenAIRE
Journal :
Journal of Experimental & Clinical Cancer Research
Accession number :
edsair.doi.dedup.....d77b39867c1572e6f406005506fabe82
Full Text :
https://doi.org/10.1186/1756-9966-32-52