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作 者:Xinxin Song Zhuan Zhou Kenneth D.Westover
机构地区:[1]Department of Surgery,University of Texas Southwestern Medical Center,Dallas,TX 75390,USA [2]Departments of Radiation Oncology and Biochemistry,University of Texas Southwestern Medical Center,Dallas,TX 75390,USA
出 处:《The Innovation》2023年第6期7-8,共2页创新(英文)
基 金:We thank Dave Primm(Department of Surgery,University of Texas Southwestern Med-ical Center)for his critical reading of the manuscript.X.S.was supported by an American Cancer Society grant(RG-21-142-16);National Institutes of Health grant(P30CA142543);Simmons Comprehensive Cancer Center and is supported by a startup fund bythe Department of Surgery at the University of Texas Southwestem Medical Center.K.D.W.is supported by grants from the National Institutes of Health(R01 CA244341);Cancer Prevention and Research Institute of Texas(RP220145).
摘 要:The Kirsten rat sarcoma(KRAS)gene,which is one of the most frequently mutated genes in human cancers,has long captured the attention of oncologists.The recent approval of KRAS G12C inhibitors(KRASi),such as sotorasib and adagrasib,has signaled a promising turn in cancer therapy.However,emerging resistance to these drugs presents a fomidable challenge.'Lv et al's2 publication in Science suggests that the proteostasis network plays a role in mediating diverse KRASi resistance mechanisms.Their work shows that KRAS inhibition suppresses protein quality control in the majority of cancer cells.In the remaining cells,a subset can reactivate one of the endoplasmic reticulum(ER)stress sensors,specifically the inositol-requiring enzyme 1 alpha(IRE1a)branch of the unfolded protein response(UPR).This adaptation enables the cells to overcome their reliance on oncogenic KRAS,enhancing their resistance to KRASi(Figure 1).This insight underscores the complex interplay be tween oncogenic signaling and protein quality control in scenarios of drug resistance.Here,we review and discuss the major findings of this study in the following sections.
关 键 词:KRAS RESISTANCE NETWORK
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