Single-cell signaling analysis reveals that Major Vault Protein facilitates RasG12C inhibitor resistance
Abstract
Recently developed covalent inhibitors for RasG12C provide the first pharmacological tools to target mutant Ras-driven cancers. However, the rapid development of resistance to current clinical Ras G12C inhibitors is common. Presumably, a subpopulation of RasG12C-expressing cells adapt their signaling to evade these inhibitors and the mechanisms for this phenomenon are unclear due to the lack of tools that can measure signaling with single-cell resolution. Here, we utilized recently developed Ras sensors to profile the environment of active Ras and to measure the activity of endogenous Ras in order to pair structure (Ras signalosome) to function (Ras activity), respectively, at a single-cell level. With this approach, we identified a subpopulation of KRasG12C cells treated with RasG12C-GDP inhibitors underwent oncogenic signaling and metabolic changes driven by WT Ras at the golgi and mutant Ras at the mitochondria, respectively. Our Ras sensors identified Major Vault Protein (MVP) as a mediator of Ras activation at both compartments by scaffolding Ras signaling pathway components and metabolite channels. We found that recently developed RasG12C-GTP inhibitors also led to MVP-mediated WT Ras signaling at the golgi, demonstrating that this a general mechanism RasG12C inhibitor resistance. Overall, single-cell analysis of structure-function relationships enabled the discovery of a RasG12C inhibitor-resistant subpopulation driven by MVP, providing insight into the complex and heterogenous rewiring occurring during drug resistance in cancer.
02 /Specification & Classification
Click any tag to browse matching papers- Organism
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Inhibitor of the nuclear transport protein XPO1 enhances the anticancer efficacy of KRAS G12C inhibitors in preclinical models of KRAS G12C mutant cancers
H. Y. Khan, M. Nagasaka, … A. S. Azmi·Cancer Research CommunicationsPeer-reviewed·May 10, 2022
- A quantitative systems pharmacology analysis of KRAS G12C covalent inhibitors
Edward C. Stites, Andréy S. Shaw·CPT Pharmacometrics & Systems PharmacologyPeer-reviewed·Feb 27, 2018
- SOS1 inhibition enhances the efficacy of and delays resistance to G12C inhibitors in lung adenocarcinoma
Brianna R. Daley, Nancy E. Sealover, … Robert L. Kortum·Cancer ResearchPeer-reviewed·Oct 22, 2024
- MRTX1133 is a potent non-covalent KRAS (G12C) inhibitor with tissue-specific activity
Abraham C. Sianoya, Yan Zuo, … Alemayehu Abebe Gorfe·Molecular Cancer TherapeuticsPeer-reviewed·Mar 14, 2026
- Engineered subtilisin protease degrades active KRAS in cancer cells, leading to differential cell targeting
M.E. Goldstein, Betty Chu, … Thomas R. Fuerst·bioRxiv·Mar 6, 2026
- Targeting Distinct Cell Cycle Nodes Overcomes KRAS/RAS Inhibitor Resistance
Vishnu Muthuraj Kumarasamy, Jianxin Wang, … Erik S. Knudsen·Cancer ResearchPeer-reviewed·Oct 2, 2026