The KRAS G12C Inhibitor MRTX849 Provides Insight toward Therapeutic Susceptibility of KRAS-Mutant Cancers in Mouse Models and Patients

Despite decades of research, efforts to directly target KRAS have been challenging. MRTX849 was identified as a potent, selective, and covalent KRAS inhibitor that exhibits favorable drug-like properties, selectively modifies mutant cysteine 12 in GDP-bound KRAS , and inhibits KRAS-dependent signali...

Full description

Saved in:

Bibliographic Details
Published in:	Cancer discovery Vol. 10; no. 1; p. 54
Main Authors:	Hallin, Jill, Engstrom, Lars D, Hargis, Lauren, Calinisan, Andrew, Aranda, Ruth, Briere, David M, Sudhakar, Niranjan, Bowcut, Vickie, Baer, Brian R, Ballard, Joshua A, Burkard, Michael R, Fell, Jay B, Fischer, John P, Vigers, Guy P, Xue, Yaohua, Gatto, Sole, Fernandez-Banet, Julio, Pavlicek, Adam, Velastagui, Karen, Chao, Richard C, Barton, Jeremy, Pierobon, Mariaelena, Baldelli, Elisa, Patricoin, 3rd, Emanuel F, Cassidy, Douglas P, Marx, Matthew A, Rybkin, Igor I, Johnson, Melissa L, Ou, Sai-Hong Ignatius, Lito, Piro, Papadopoulos, Kyriakos P, Jänne, Pasi A, Olson, Peter, Christensen, James G
Format:	Journal Article
Language:	English
Published:	United States 01-01-2020
Subjects:	Acetonitriles - therapeutic use Adenocarcinoma of Lung - drug therapy Adenocarcinoma of Lung - genetics Adenocarcinoma of Lung - pathology Animals Antineoplastic Agents - therapeutic use Apoptosis Cell Proliferation Clinical Trials, Phase I as Topic Disease Models, Animal Female Humans Lung Neoplasms - drug therapy Lung Neoplasms - genetics Lung Neoplasms - pathology Mice Mice, Inbred BALB C Mice, Inbred NOD Mice, Nude Mice, SCID Middle Aged Mutation Piperazines - therapeutic use Prognosis Proto-Oncogene Proteins p21(ras) - antagonists & inhibitors Proto-Oncogene Proteins p21(ras) - genetics Pyrrolidines - therapeutic use Signal Transduction Tumor Cells, Cultured Xenograft Model Antitumor Assays
Online Access:	Get more information
Tags:	Add Tag No Tags, Be the first to tag this record!

Description
Summary:	Despite decades of research, efforts to directly target KRAS have been challenging. MRTX849 was identified as a potent, selective, and covalent KRAS inhibitor that exhibits favorable drug-like properties, selectively modifies mutant cysteine 12 in GDP-bound KRAS , and inhibits KRAS-dependent signaling. MRTX849 demonstrated pronounced tumor regression in 17 of 26 (65%) KRAS -positive cell line- and patient-derived xenograft models from multiple tumor types, and objective responses have been observed in patients with KRAS -positive lung and colon adenocarcinomas. Comprehensive pharmacodynamic and pharmacogenomic profiling in sensitive and partially resistant nonclinical models identified mechanisms implicated in limiting antitumor activity including KRAS nucleotide cycling and pathways that induce feedback reactivation and/or bypass KRAS dependence. These factors included activation of receptor tyrosine kinases (RTK), bypass of KRAS dependence, and genetic dysregulation of cell cycle. Combinations of MRTX849 with agents that target RTKs, mTOR, or cell cycle demonstrated enhanced response and marked tumor regression in several tumor models, including MRTX849-refractory models. SIGNIFICANCE: The discovery of MRTX849 provides a long-awaited opportunity to selectively target KRAS in patients. The in-depth characterization of MRTX849 activity, elucidation of response and resistance mechanisms, and identification of effective combinations provide new insight toward KRAS dependence and the rational development of this class of agents. . .
ISSN:	2159-8290