Abstract 7637: Genome-wide CRISPR screening reveals a PKA-driven resistance mechanism to metformin for oral cancer prevention that can be exploited by combination with NSAIDs

Abstract Head and neck squamous cell carcinoma (HNSCC) is among the ten most common cancers worldwide and is associated with high morbidity and poor survival. Diminished HNSCC outcomes are often related to delayed diagnosis and treatment of occult progression of premalignant lesions, underscoring the need for effective and low risk chemoprevention strategies. In this regard, metformin has shown promising clinical activity for HNSCC prevention. Here, we performed a genome-wide CRISPR/Cas9 screen of metformin-treated HNSCC cells and identified activation of PKA signaling as the top resistance pathway. We show that metformin mediates PKA activation in HNSCC cells, and that PKA inhibition (PKAi) when combined with metformin treatment synergistically inhibits HNSCC growth. We found that metformin-induced PKA activation is mediated by a prostaglandin E2 (PGE2) autocrine loop, which can be blocked using cyclooxygenase-2 (COX2) inhibitors. Importantly, COX2 inhibition using non-steroidal anti-inflammatory drugs (NSAIDs) combined with metformin treatment synergistically inhibits of HNSCC cell growth and prevents progression of oral premalignant lesions (OPLs) into invasive HNSCC in a model of tobacco driven oral carcinogenesis. Together, these findings demonstrate that metformin and NSAID combination therapy may represent a promising therapeutic strategy for HNSCC chemoprevention. Citation Format: Thomas S. Hoang, Farhoud Faraji, Amaya Mendez-Molina, Sendi R. Adame-Garcia, Kuniaki Sato, Tomohiko Ishikawa, Pham Thuy Vo, Sydney Ramirez, Paola Y. Anguiano Quiroz, Tracy Guo, Katie Fan, Xingyu Wu, Alfredo Molinolo, Ezra E. W. Cohen, Prashant Mali, Scott M. Lippman, J. Silvio Gutkind. Genome-wide CRISPR screening reveals a PKA-driven resistance mechanism to metformin for oral cancer prevention that can be exploited by combination with NSAIDs [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 7637.

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Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-7637
Primary Topic
Metabolism, Diabetes, and Cancer
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article

Abstract 7637: Genome-wide CRISPR screening reveals a PKA-driven resistance mechanism to metformin for oral cancer prevention that can be exploited by combination with NSAIDs

Ezra E.W. Cohen, Sendi Rafael Adame-Garcia, Kuniaki Sato, Paola Y. Anguiano Quiroz et al.
Cancer Research
Metabolism, Diabetes, and Cancer
article

Abstract 7637: Genome-wide CRISPR screening reveals a PKA-driven resistance mechanism to metformin for oral cancer prevention that can be exploited by combination with NSAIDs

Ezra E.W. Cohen, Sendi Rafael Adame-Garcia, Kuniaki Sato, Paola Y. Anguiano Quiroz, Sydney I. Ramirez, Amaya N. Mendez-Molina, Farhoud Faraji, Scott M. Lippman, Prashant Mali, Xingyu Wu, Tracy Guo, Pham Thuy Vo, Thomas S. Hoang, Alfredo Molinolo, Katie Fan, J. Silvio Gutkind, Tomohiko Ishikawa
article en

Abstract

Abstract Head and neck squamous cell carcinoma (HNSCC) is among the ten most common cancers worldwide and is associated with high morbidity and poor survival. Diminished HNSCC outcomes are often related to delayed diagnosis and treatment of occult progression of premalignant lesions, underscoring the need for effective and low risk chemoprevention strategies. In this regard, metformin has shown promising clinical activity for HNSCC prevention. Here, we performed a genome-wide CRISPR/Cas9 screen of metformin-treated HNSCC cells and identified activation of PKA signaling as the top resistance pathway. We show that metformin mediates PKA activation in HNSCC cells, and that PKA inhibition (PKAi) when combined with metformin treatment synergistically inhibits HNSCC growth. We found that metformin-induced PKA activation is mediated by a prostaglandin E2 (PGE2) autocrine loop, which can be blocked using cyclooxygenase-2 (COX2) inhibitors. Importantly, COX2 inhibition using non-steroidal anti-inflammatory drugs (NSAIDs) combined with metformin treatment synergistically inhibits of HNSCC cell growth and prevents progression of oral premalignant lesions (OPLs) into invasive HNSCC in a model of tobacco driven oral carcinogenesis. Together, these findings demonstrate that metformin and NSAID combination therapy may represent a promising therapeutic strategy for HNSCC chemoprevention. Citation Format: Thomas S. Hoang, Farhoud Faraji, Amaya Mendez-Molina, Sendi R. Adame-Garcia, Kuniaki Sato, Tomohiko Ishikawa, Pham Thuy Vo, Sydney Ramirez, Paola Y. Anguiano Quiroz, Tracy Guo, Katie Fan, Xingyu Wu, Alfredo Molinolo, Ezra E. W. Cohen, Prashant Mali, Scott M. Lippman, J. Silvio Gutkind. Genome-wide CRISPR screening reveals a PKA-driven resistance mechanism to metformin for oral cancer prevention that can be exploited by combination with NSAIDs [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 7637.

Cancer ResearchVol. 86(7_Supplement)
La Jolla Institute for Immunology (US), La Jolla Alcohol Research (US), Moores Cancer Center
Good health and well-being
Openalex Percentile: Top 30%
Metabolism, Diabetes, and Cancer
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