Kras(g12c) Inhibitors on the Horizon
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Date
2019
Authors
Çağır, Ali
Journal Title
Journal ISSN
Volume Title
Publisher
Future Science
Open Access Color
BRONZE
Green Open Access
No
OpenAIRE Downloads
OpenAIRE Views
Publicly Funded
No
Abstract
RAS proteins (the four isoforms KRAS4A, KRAS4B, NRAS and HRAS encoded by three genes KRAS, NRAS and HRAS) act as molecular switches that when activated drive several key cellular processes such as cell growth, proliferation and survival [1]. In normal cells, RAS activity is under tight control by the precise activation (binding to GTP) and inactivation (GTP hydrolysis to GDP) [1]. As with other critical proteins, it is not at all surprising to note that the gene encoding the RAS protein isoforms is found mutated or altered in a significant proportion of tumors [2]. Mutant RAS loses its ability to hydrolyze GTP and remains in a permanently activated state (bound to GTP) leading to uncontrolled growth.
Description
Keywords
Inhibitors, KRAS, KRAS(G12C), KRAS(G12D), RAS, Therapy resistance, Proto-Oncogene Proteins p21(ras), Small Molecule Libraries, Drug Development, Drug Discovery, Animals, Humans, Point Mutation, Guanosine Triphosphate
Fields of Science
0301 basic medicine, 0303 health sciences, 03 medical and health sciences
Citation
WoS Q
Q2
Scopus Q
Q3

OpenCitations Citation Count
7
Source
Future Medicinal Chemistry
Volume
11
Issue
9
Start Page
923
End Page
925
PlumX Metrics
Citations
CrossRef : 7
Scopus : 9
PubMed : 7
Captures
Mendeley Readers : 7
SCOPUS™ Citations
9
checked on Apr 27, 2026
Web of Science™ Citations
8
checked on Apr 27, 2026
Page Views
899
checked on Apr 27, 2026
Downloads
283
checked on Apr 27, 2026
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