A holistic view on c-Kit in cancer: Structure, signaling, pathophysiology and its inhibitors




Pathania Shelly, Pentikäinen Olli T, Singh Pankaj Kumar

PublisherELSEVIER

2021

BBA - Reviews on Cancer

BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER

BBA-REV CANCER

ARTN 188631

1876

2

21

0304-419X

1879-2561

DOIhttps://doi.org/10.1016/j.bbcan.2021.188631

https://www.sciencedirect.com/science/article/pii/S0304419X21001293?via%3Dihub

https://research.utu.fi/converis/portal/detail/Publication/67765444



Receptor tyrosine kinases play an important role in many cellular processes, and their dysregulation leads to diseases, most importantly cancer. One such receptor tyrosine kinase is c-Kit, a type-III receptor tyrosine kinase, which is involved in various intracellular signaling pathways. The role of different mutant isoforms of c-Kit has been established in several types of cancers. Accordingly, promising c-Kit inhibition results have been reported for the treatment of different cancers (e.g., gastrointestinal stromal tumors, melanoma, acute myeloid leukemia, and other tumors). Therefore, lots of effort has been put to target c-Kit for the treatment of cancer. Here, we provide a comprehensive compilation to provide an insight into c-Kit inhibitor discovery. This compilation provides key information regarding the structure, signaling pathways related to c-Kit, and, more importantly, pharmacophores, binding modes, and SAR analysis for almost all small-molecule heterocycles reported for their c-Kit inhibitory activity. This work could be used as a guide in understanding the basic requirements for targeting c-Kit, and how the selectivity and efficacy of the molecules have been achieved till today.

Last updated on 2024-26-11 at 21:37