| Literature DB >> 32008085 |
Reza Mohammadinejad1, Alessio Biagioni2, Ganesan Arunkumar3, Rebecca Shapiro4, Kun-Che Chang5, Mohammed Sedeeq6, Aftab Taiyab7, Mohammad Hashemabadi8,9, Abbas Pardakhty10, Ali Mandegary11, Jean-Paul Thiery12, Amir Reza Aref13, Iman Azimi14.
Abstract
Epithelial to mesenchymal transition (EMT) is a complex plastic and reversible cellular process that has critical roles in diverse physiological and pathological phenomena. EMT is involved in embryonic development, organogenesis and tissue repair, as well as in fibrosis, cancer metastasis and drug resistance. In recent years, the ability to edit the genome using the clustered regularly interspaced palindromic repeats (CRISPR) and associated protein (Cas) system has greatly contributed to identify or validate critical genes in pathway signaling. This review delineates the complex EMT networks and discusses recent studies that have used CRISPR/Cas technology to further advance our understanding of the EMT process.Entities:
Keywords: CRISPR; Cancer; Epithelial–mesenchymal transition; Gene editing
Mesh:
Year: 2020 PMID: 32008085 DOI: 10.1007/s00018-020-03449-3
Source DB: PubMed Journal: Cell Mol Life Sci ISSN: 1420-682X Impact factor: 9.261