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KRAS Inhibition in Pancreatic Ductal Adenocarcinoma

Roshini Pradeep, Nooredeen Isbeih, Freya F. Abraham, Ehsan Noori, Zachary P Yeung, Madappa N. Kundranda

2026Journal of Clinical Medicine5 citationsDOIOpen Access PDF

Abstract

KRAS alterations are a hallmark of pancreatic ductal adenocarcinoma (PDAC) found in >90% of tumors. This review examines the historical evolution of the understanding of RAS and its central role in PDAC biology. We summarize the various downstream effectors, feedback loops, and resistance mechanisms that play a pivotal role in PDAC oncogenesis. Our review explores the early development of covalent inhibitors of KRAS G12C and efforts at specific inhibition of other codons and newer approaches of targeted protein degradation. We subsequently summarize the development of panRAS inhibitors and allosteric and switch-region targeting before focusing on rational therapeutic blockade of crosstalk and upstream signaling, with attention to synthetic lethality approaches transitioning from preclinical to early-phase in-human clinical trials. This review elaborates on ongoing KRAS-specific siRNA research and evolving KRAS-directed immunotherapies. We conclude by outlining the current KRAS clinical trial landscape and future areas of investigation.

Topics & Concepts

KRASMedicinePancreatic ductal adenocarcinomaBlockadeCancer researchCrosstalkPancreatic cancerClinical trialTargeted therapyBioinformaticsEffectorAllosteric regulationAcquired resistanceMolecular oncologyCancerSynthetic lethalityMetastasisAdenocarcinomaSuppressorTherapeutic approachOncologyPhenotypeProtein Kinase Regulation and GTPase SignalingPeptidase Inhibition and AnalysisPancreatic and Hepatic Oncology Research