| Literature DB >> 25139999 |
Clémence Feneyrolles1, Aurélia Spenlinhauer1, Léa Guiet1, Bénédicte Fauvel1, Bénédicte Daydé-Cazals1, Pierre Warnault1, Gwénaël Chevé1, Aziz Yasri2.
Abstract
Receptor tyrosine kinases (RTK) are transmembrane receptors that regulate signal transduction in cells. As a member of the TAM (Tyro-3, Axl, Mer) RTK subfamily, Axl regulates key processes such as cell growth, migration, aggregation, and apoptosis through several pathways. Its overexpression/overactivation has been underlined in several conditions, especially cancers, and in both chemotherapy and targeted therapy sensitivity loss. In this review, we propose to highlight the therapeutic implication of Axl, starting with the pathways it regulates, validating its interest as a therapeutic target, and defining the tools available to develop strategies for its inhibition. We especially focus on small molecule inhibitors, their structure, inhibition profile, and development stages. ©2014 American Association for Cancer Research.Entities:
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Year: 2014 PMID: 25139999 DOI: 10.1158/1535-7163.MCT-13-1083
Source DB: PubMed Journal: Mol Cancer Ther ISSN: 1535-7163 Impact factor: 6.261