Back to Search Start Over

Hepatocyte Growth Factor/cMET Pathway Activation Enhances Cancer Hallmarks in Adrenocortical Carcinoma.

Authors :
Phan LM
Fuentes-Mattei E
Wu W
Velazquez-Torres G
Sircar K
Wood CG
Hai T
Jimenez C
Cote GJ
Ozsari L
Hofmann MC
Zheng S
Verhaak R
Pagliaro L
Cortez MA
Lee MH
Yeung SC
Habra MA
Source :
Cancer research [Cancer Res] 2015 Oct 01; Vol. 75 (19), pp. 4131-42. Date of Electronic Publication: 2015 Aug 17.
Publication Year :
2015

Abstract

Adrenocortical carcinoma is a rare malignancy with poor prognosis and limited response to chemotherapy. Hepatocyte growth factor (HGF) and its receptor cMET augment cancer growth and resistance to chemotherapy, but their role in adrenocortical carcinoma has not been examined. In this study, we investigated the association between HGF/cMET expression and cancer hallmarks of adrenocortical carcinoma. Transcriptomic and immunohistochemical analyses indicated that increased HGF/cMET expression in human adrenocortical carcinoma samples was positively associated with cancer-related biologic processes, including proliferation and angiogenesis, and negatively correlated with apoptosis. Accordingly, treatment of adrenocortical carcinoma cells with exogenous HGF resulted in increased cell proliferation in vitro and in vivo while short hairpin RNA-mediated knockdown or pharmacologic inhibition of cMET suppressed cell proliferation and tumor growth. Moreover, exposure of cells to mitotane, cisplatin, or radiation rapidly induced pro-cMET expression and was associated with an enrichment of genes (e.g., CYP450 family) related to therapy resistance, further implicating cMET in the anticancer drug response. Together, these data suggest an important role for HGF/cMET signaling in adrenocortical carcinoma growth and resistance to commonly used treatments. Targeting cMET, alone or in combination with other drugs, could provide a breakthrough in the management of this aggressive cancer.<br /> (©2015 American Association for Cancer Research.)

Details

Language :
English
ISSN :
1538-7445
Volume :
75
Issue :
19
Database :
MEDLINE
Journal :
Cancer research
Publication Type :
Academic Journal
Accession number :
26282167
Full Text :
https://doi.org/10.1158/0008-5472.CAN-14-3707