Novel clinical therapeutics targeting the epithelial to mesenchymal transition

Clinical and Translational Medicine

Zhiyong Mi¹  Paul C Kuo¹  Anai N Kothari¹  Matthew Zapf¹ 

[1] Department of SurgeryOncology InstituteLoyola University Medical CenterRm 3244, 2160 South First Ave, EMS Bldg60153MaywoodILUSA;

关键词: Epithelial mesenchymal transition (EMT);    Small molecule inhibitors;    TGFβ;    Cancer associated fibroblasts;   

DOI  :  10.1186/s40169-014-0035-0

来源: DOAJ

【 摘 要 】

Abstract The epithelial to mesenchymal transition (EMT) is implicated in many processes, ranging from tissue and organogenesis to cancer and metastatic spread. Understanding the key regulatory mechanisms and mediators within this process offers the opportunity to develop novel therapeutics with broad clinical applicability. To date, several components of EMT already are targeted using pharmacologic agents in fibrosis and cancer. As our knowledge of EMT continues to grow, the potential for novel therapeutics will also increase. This review focuses on the role of EMT both as a necessary part of development and a key player in disease progression, specifically the similarity in pathways used during both processes as targets for drug development. Also, the key role of the tumor microenvironment with EMT is outlined, focusing on both co‐factors and cell types with the ability to modulate the progression of EMT in cancer and metastatic disease. Lastly, we discuss the current status of clinical therapies both in development and those progressed to clinical trial specifically targeting pathologic EMTs including small molecule inhibitors, non‐coding RNAs, exogenous co‐factors, and adjunctive therapies to current chemotherapeutics.

【 授权许可】

Unknown