| Literature DB >> 30607625 |
Harikrishnan Radhakrishnan1, Wolfgang Walther1,2, Fabian Zincke1,2, Dennis Kobelt1,2, Francesca Imbastari1, Müge Erdem1, Benedikt Kortüm1, Mathias Dahlmann1,2, Ulrike Stein3,4.
Abstract
Deciphering the paths to metastasis and identifying key molecules driving this process is one important issue for understanding and treatment of cancer. Such a key driver molecule is Metastasis Associated in Colon Cancer 1 (MACC1). A decade long research on this evolutionarily conserved molecule with features of a transcription factor as well as an adapter protein for versatile protein-protein interactions has shown that it has manifold properties driving tumors to their metastatic stage. MACC1 transcriptionally regulates genes involved in epithelial-mesenchymal transition (EMT), including those which are able to directly induce metastasis like c-MET, impacts tumor cell migration and invasion, and induces metastasis in solid cancers. MACC1 has proven as a valuable biomarker for prognosis of metastasis formation linked to patient survival and gives promise to also act as a predictive marker for individualized therapies in a broad variety of cancers. This review discusses the many features of MACC1 in the context of the hallmarks of cancer and the potential of this molecule as biomarker and novel therapeutic target for restriction and prevention of metastasis.Entities:
Keywords: MACC1; biomarker; metastasis; prognosis and prediction; solid cancers; targeted therapy
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Year: 2018 PMID: 30607625 DOI: 10.1007/s10555-018-9771-8
Source DB: PubMed Journal: Cancer Metastasis Rev ISSN: 0167-7659 Impact factor: 9.264