| Literature DB >> 29634387 |
John C Rose1, Emily M Dieter1, Daniel Cunningham-Bryant1, Dustin J Maly1,2.
Abstract
RAS signaling pathways govern diverse cellular processes, are dynamic, and exhibit marked plasticity. Yet, these features also present a considerable obstacle to their study. Here, we report the use of a recently described RAS rheostat, Chemically Inducible Activator of RAS (CIAR), to study two poorly understood phenomena in RAS biology. First, we show that short-term activation of wild type endogenous RAS can desensitize cells to EGF stimulation. Second, we examine the phenomena of paradoxical activation of RAS/ERK signaling by RAF inhibitors. Specifically, we characterize the effects on RAS/ERK signaling kinetics of four RAF inhibitors, which stabilize distinct ATP-binding site conformations. These results demonstrate the utility of CIAR in conducting quantitative studies of complex features of RAS biology.Entities:
Mesh:
Substances:
Year: 2018 PMID: 29634387 PMCID: PMC7549627 DOI: 10.1080/21541248.2018.1446697
Source DB: PubMed Journal: Small GTPases ISSN: 2154-1248