| Literature DB >> 24823640 |
Alvaro Aytes1,2, Antonina Mitrofanova3, Celine Lefebvre3, Mariano J Alvarez3, Mireia Castillo-Martin4, Tian Zheng5,6, James A Eastham7, Anuradha Gopalan8, Kenneth J Pienta9, Michael M Shen1,3,10,11,5, Andrea Califano3,12,5, Cory Abate-Shen1,3,13,5.
Abstract
To identify regulatory drivers of prostate cancer malignancy, we have assembled genome-wide regulatory networks (interactomes) for human and mouse prostate cancer from expression profiles of human tumors and of genetically engineered mouse models, respectively. Cross-species computational analysis of these interactomes has identified FOXM1 and CENPF as synergistic master regulators of prostate cancer malignancy. Experimental validation shows that FOXM1 and CENPF function synergistically to promote tumor growth by coordinated regulation of target gene expression and activation of key signaling pathways associated with prostate cancer malignancy. Furthermore, co-expression of FOXM1 and CENPF is a robust prognostic indicator of poor survival and metastasis. Thus, genome-wide cross-species interrogation of regulatory networks represents a valuable strategy to identify causal mechanisms of human cancer.Entities:
Mesh:
Substances:
Year: 2014 PMID: 24823640 PMCID: PMC4051317 DOI: 10.1016/j.ccr.2014.03.017
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 31.743