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Hepatocyte Growth Factor/cMET Pathway Activation Enhances Cancer Hallmarks in Adrenocortical Carcinoma.
- 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.)
- Subjects :
- Adenoma drug therapy
Adenoma metabolism
Adenoma pathology
Adrenal Cortex Neoplasms blood supply
Adrenal Cortex Neoplasms drug therapy
Adrenal Cortex Neoplasms pathology
Adult
Aged
Aged, 80 and over
Anilides pharmacology
Anilides therapeutic use
Animals
Antineoplastic Agents pharmacology
Antineoplastic Agents therapeutic use
Carcinoma blood supply
Carcinoma drug therapy
Carcinoma pathology
Cell Division
Cell Line, Tumor
Cisplatin pharmacology
Drug Resistance, Neoplasm drug effects
Drug Resistance, Neoplasm radiation effects
Female
Gene Expression Profiling
Gene Expression Regulation, Neoplastic drug effects
Gene Expression Regulation, Neoplastic radiation effects
Humans
Male
Mice
Mice, Nude
Middle Aged
Mitotane pharmacology
Molecular Targeted Therapy
Neovascularization, Pathologic physiopathology
Pyridines pharmacology
Pyridines therapeutic use
RNA Interference
RNA, Small Interfering pharmacology
Transcriptome
Xenograft Model Antitumor Assays
Adrenal Cortex Neoplasms metabolism
Carcinoma metabolism
Hepatocyte Growth Factor physiology
Neoplasm Proteins physiology
Proto-Oncogene Proteins c-met physiology
Signal Transduction physiology
Subjects
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