Abstract PR005: <i>KRAS</i> amplification as <i>de novo</i> oncogenic alteration and therapeutic target in human cancers

Abstract KRAS mutations are established oncogenic drivers and resistance mechanisms, but the biological and clinical significance of KRAS gene amplification (KRASAMP) is poorly understood. Here, we integrate genomic, structural, clinical, and functional data to show that KRASAMP is a recurrent de novo driver alteration and therapeutic vulnerability across human cancers. In three independent clinico-genomic datasets totaling 685,507 tumors, KRASAMP occurred in ∼2-3% of cancers, with enrichment in esophagogastric, germ cell, ovarian, non-small cell lung, colorectal, biliary tract, pancreatic, and breast cancers. High-level KRASAMP was largely mutually exclusive with canonical oncogenic drivers, and increasing KRAS copy number inversely correlated with the prevalence of alternative drivers, supporting KRASAMP as an independent oncogenic event. KRAS copy gains tightly correlated with increased KRAS mRNA and protein expression and with poorer overall survival across tumor types, irrespective of KRAS mutation status. Whole-genome sequencing and FISH revealed heterogeneous amplicon architectures, including extrachromosomal DNA and linear chromosomal configurations. In Rasless cells, forced overexpression of wild-type KRAS alone restored MAPK signaling, rescued proliferation, and conferred sensitivity to the mutation-agnostic pan-RAS inhibitor RMC-7977. These data establish KRAS amplification as a de novo, targetable oncogenic driver in human cancer. Citation Format: Mark M. Awad, Biagio Ricciuti, Sandra Vietti Michelina, Edoardo Garbo, Paolo Tarantino, Alok Tewari, Igor Odintsov, Xinan Wang, Cassio Murilo Trovo Hidalgo Filho, Nishant Gandhi, Kenneth Kehl, Giuseppe Lamberti, Alessandro Di Federico, Malini Gandhi, Federica Pecci, Mihaela Aldea, Valentina Santo, Eleonora Gariazzo, Lynette Sholl, Stefano Scalera, Marcello Maugeri, Nancy Lin, Federico Cappuzzo, Pasi Janne, Steven Ressler, Marzia Capelletti, Alexa Schrock, Toni Choueiri, Julie Wiese, Debbie Liao, Shailaja Kasibhatla, Sara Tolaney, Andrew Aguirre, Alice Shaw, Chiara Ambrogio. KRAS amplification as de novo oncogenic alteration and therapeutic target in human cancers [abstract]. In: Proceedings of the AACR Special Conference in Cancer Research: RAS Oncogenesis and Therapeutics; 2026 Mar 5-8; Los Angeles, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(5_Suppl_1):Abstract nr PR005.

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Journal
Cancer Research
Published
2026-03-05
DOI
https://doi.org/10.1158/1538-7445.rasoncother26-pr005
Primary Topic
Protein Kinase Regulation and GTPase Signaling
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article
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article

Abstract PR005: KRAS amplification as de novo oncogenic alteration and therapeutic target in human cancers

Steven J. Ressler, Edoardo Garbo, Cássio Murilo Trovo Hidalgo Filho, M. Aldea et al.
Cancer Research
Protein Kinase Regulation and GTPase Signaling
article

Abstract PR005: KRAS amplification as de novo oncogenic alteration and therapeutic target in human cancers

Steven J. Ressler, Edoardo Garbo, Cássio Murilo Trovo Hidalgo Filho, M. Aldea, Julie Wiese, Alexa B. Schrock, Kenneth L. Kehl, Malini Gandhi, Andrew J. Aguirre, Sandra Vietti Michelina, Giuseppe Lamberti, Shailaja Kasibhatla, Paolo Tarantino, N. Gandhi, Eleonora Gariazzo, Nancy L. Lin, Debbie Liao, A. Shaw, Pasi A. Jänne, Mark M. Awad, Xinan Wang, Federica Pecci, Valentina Santo, Marcello Maugeri, Alok Tewari, Igor Odintsov, Marzia Capelletti, Stefano Scalera, Lynette Sholl
article en

Abstract

Abstract KRAS mutations are established oncogenic drivers and resistance mechanisms, but the biological and clinical significance of KRAS gene amplification (KRASAMP) is poorly understood. Here, we integrate genomic, structural, clinical, and functional data to show that KRASAMP is a recurrent de novo driver alteration and therapeutic vulnerability across human cancers. In three independent clinico-genomic datasets totaling 685,507 tumors, KRASAMP occurred in ∼2-3% of cancers, with enrichment in esophagogastric, germ cell, ovarian, non-small cell lung, colorectal, biliary tract, pancreatic, and breast cancers. High-level KRASAMP was largely mutually exclusive with canonical oncogenic drivers, and increasing KRAS copy number inversely correlated with the prevalence of alternative drivers, supporting KRASAMP as an independent oncogenic event. KRAS copy gains tightly correlated with increased KRAS mRNA and protein expression and with poorer overall survival across tumor types, irrespective of KRAS mutation status. Whole-genome sequencing and FISH revealed heterogeneous amplicon architectures, including extrachromosomal DNA and linear chromosomal configurations. In Rasless cells, forced overexpression of wild-type KRAS alone restored MAPK signaling, rescued proliferation, and conferred sensitivity to the mutation-agnostic pan-RAS inhibitor RMC-7977. These data establish KRAS amplification as a de novo, targetable oncogenic driver in human cancer. Citation Format: Mark M. Awad, Biagio Ricciuti, Sandra Vietti Michelina, Edoardo Garbo, Paolo Tarantino, Alok Tewari, Igor Odintsov, Xinan Wang, Cassio Murilo Trovo Hidalgo Filho, Nishant Gandhi, Kenneth Kehl, Giuseppe Lamberti, Alessandro Di Federico, Malini Gandhi, Federica Pecci, Mihaela Aldea, Valentina Santo, Eleonora Gariazzo, Lynette Sholl, Stefano Scalera, Marcello Maugeri, Nancy Lin, Federico Cappuzzo, Pasi Janne, Steven Ressler, Marzia Capelletti, Alexa Schrock, Toni Choueiri, Julie Wiese, Debbie Liao, Shailaja Kasibhatla, Sara Tolaney, Andrew Aguirre, Alice Shaw, Chiara Ambrogio. KRAS amplification as de novo oncogenic alteration and therapeutic target in human cancers [abstract]. In: Proceedings of the AACR Special Conference in Cancer Research: RAS Oncogenesis and Therapeutics; 2026 Mar 5-8; Los Angeles, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(5_Suppl_1):Abstract nr PR005.

Cancer ResearchVol. 86(5_Supplement_1)
Brigham and Women's Hospital (US), Memorial Sloan Kettering Cancer Center (US), GlobalFoundries (United States) (US), Kettering University (US), Boundless Bio (United States) (US), Dana-Farber Cancer Institute (US), National Cancer Institute (MY), Caris Life Sciences (United States) (US)
No poverty
Openalex Percentile: Top 32%
Protein Kinase Regulation and GTPase Signaling
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