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Hormonal-receptor positive breast cancer: IL-6 augments invasion and lymph node metastasis via stimulating cathepsin B expression

Authors :
Noha Mahana
Tahani El-Mamlouk
Eslam A. El-Ghonaimy
Hebatallah Hassan
Mona Mostafa Mohamed
Sherif Abdelaziz Ibrahim
Mahmoud A Mahmoud
Mohamed El-Shinawi
Source :
Journal of Advanced Research, Journal of Advanced Research, Vol 7, Iss 5, Pp 661-670 (2016)
Publication Year :
2016
Publisher :
Elsevier BV, 2016.

Abstract

Graphical abstract<br />Hormonal-receptor positive (HRP) breast cancer patients with positive metastatic axillary lymph nodes are characterized by poor prognosis and increased mortality rate. The mechanisms by which cancer cells invade lymph nodes have not yet been fully explored. Several studies have shown that expression of IL-6 and the proteolytic enzyme cathepsin B (CTSB) was associated with breast cancer poor prognosis. In the present study, the effect of different concentrations of recombinant human IL-6 on the invasiveness capacity of HRP breast cancer cell line MCF-7 was tested using an in vitro invasion chamber assay. The impact of IL-6 on expression and activity of CTSB was also investigated. IL-6 treatment promoted the invasiveness potential of MCF-7 cells in a dose-dependent manner. Furthermore, MCF-7 cells displayed elevated CTSB expression and activity associated with loss of E-cadherin and upregulation of vimentin protein levels upon IL-6 stimulation. To validate these results in vivo, the level of expression of IL-6 and CTSB in the carcinoma tissues of HRP-breast cancer patients with positive and negative axillary metastatic lymph nodes (pLNs and nLNs) was assessed. Western blot and immunohistochemical staining data showed that expression of IL-6 and CTSB was higher in carcinoma tissues in HRP-breast cancer with pLNs than those with nLNs patients. ELISA results showed carcinoma tissues of HRP-breast cancer with pLNs exhibited significantly elevated IL-6 protein levels by approximately 2.8-fold compared with those with nLNs patients (P

Details

ISSN :
20901232
Volume :
7
Database :
OpenAIRE
Journal :
Journal of Advanced Research
Accession number :
edsair.doi.dedup.....a19da3ff70b0bc5ebdeef69ea5081d87