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Following MicroRNAs Through the Cancer Metastatic Cascade.
- Source :
-
International review of cell and molecular biology [Int Rev Cell Mol Biol] 2017; Vol. 333, pp. 173-228. Date of Electronic Publication: 2017 Jun 07. - Publication Year :
- 2017
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Abstract
- Approximately a decade ago the first MicroRNAs (MiRNAs) participating in cancer metastasis were identified and metastmiRs were initially only a handful. Since those first reports, MiRNA research has explosively thrived, mainly due to their revolutionary mechanism of action and the hope of having at hand a novel tool to control cancer aggressiveness. This has ultimately led to delineate an almost impenetrable regulatory network: hundreds of MiRNAs transversally dominating every aspect of normal and cancer biology, each MiRNA having hundreds of targets and context-dependent activity. Providing a comprehensive description of MiRNA roles in cancer metastasis is a daunting task; nevertheless, we still believe that grasping the big picture of MiRNAs in cancer metastasis can give a different perspective on the potential insights and approaches that MiRNAs can offer to understand cancer complexity (e.g., as predictive and prognostic markers) and to tackle cancer metastasis (e.g., as therapeutic targets or tools). This chapter presents a schematic overview of the role of MiRNAs in governing cancer metastasis, describing step by step the cellular and molecular processes whereby cancer cells conquer distant organs and can grow as secondary tumors at different distant sites, and for each step, we will introduce how MiRNAs impinge on each one of them. We deeply apologize with our colleagues for any of their research work that, for clarity, for our effort to streamline and due to space limitations, we did not cite.<br /> (© 2017 Elsevier Inc. All rights reserved.)
Details
- Language :
- English
- ISSN :
- 1937-6448
- Volume :
- 333
- Database :
- MEDLINE
- Journal :
- International review of cell and molecular biology
- Publication Type :
- Academic Journal
- Accession number :
- 28729025
- Full Text :
- https://doi.org/10.1016/bs.ircmb.2017.04.005