| Literature DB >> 26077471 |
Sara I Cunha1, Matteo Bocci2, John Lövrot3, Nikolas Eleftheriou2, Pernilla Roswall4, Eugenia Cordero2, Linda Lindström3, Michael Bartoschek2, B Kristian Haller4, R Scott Pearsall5, Aaron W Mulivor5, Ravindra Kumar5, Christer Larsson2, Jonas Bergh3, Kristian Pietras6.
Abstract
Exploration of new strategies for the prevention of breast cancer metastasis is justifiably at the center of clinical attention. In this study, we combined a computational biology approach with mechanism-based preclinical trials to identify inhibitors of activin-like receptor kinase (ALK) 1 as effective agents for blocking angiogenesis and metastasis in breast cancer. Pharmacologic targeting of ALK1 provided long-term therapeutic benefit in mouse models of mammary carcinoma, accompanied by strikingly reduced metastatic colonization as a monotherapy or part of combinations with chemotherapy. Gene-expression analysis of breast cancer specimens from a population-based nested case-control study encompassing 768 subjects defined endothelial expression of ALK1 as an independent and highly specific prognostic factor for metastatic manifestation, a finding that was corroborated in an independent clinical cohort. Overall, our results suggest that pharmacologic inhibition of endothelial ALK1 constitutes a tractable strategy for interfering with metastatic dissemination of breast cancer. ©2015 American Association for Cancer Research.Entities:
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Year: 2015 PMID: 26077471 DOI: 10.1158/0008-5472.CAN-14-3706
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701