| Literature DB >> 26282167 |
Liem M Phan1, Enrique Fuentes-Mattei2, Weixin Wu3, Guermarie Velazquez-Torres4, Kanishka Sircar2, Christopher G Wood5, Tao Hai6, Camilo Jimenez6, Gilbert J Cote6, Levent Ozsari6, Marie-Claude Hofmann6, Siyuan Zheng7, Roeland Verhaak8, Lance Pagliaro9, Maria Angelica Cortez10, Mong-Hong Lee11, Sai-Ching J Yeung12, Mouhammed Amir Habra13.
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. ©2015 American Association for Cancer Research.Entities:
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Year: 2015 PMID: 26282167 PMCID: PMC4592476 DOI: 10.1158/0008-5472.CAN-14-3707
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701