Genome-wide CRISPR screen identifies AMBRA1 as a potential biomarker of response to platinum-based therapies in oral squamous cell carcinomas
Oral squamous cell carcinomas (OSCCs) are among the most frequent and lethal cancers worldwide. Advanced stage tumors are still treated with standard chemotherapy; however, most patients develop chemotherapy resistance. To uncover new functional biomarkers of cisplatin response, we performed a synthetic lethality genome-wide CRISPR-Cas9 screen in an OSCC cell line. This led to the discovery of AMBRA1 as a regulator of cisplatin sensitivity. In all tested OSCC cell lines and oral primary culture, AMBRA1 knockout cells showed increased sensitivity to cisplatin. Mechanistically, we demonstrated an unknown function of AMBRA1 in OSCCs, where loss of AMBRA1 led to an increase in S phase population, expression of genome instability markers, and DNA damage in basal conditions, predisposing cancer cells to an increased sensitivity to cisplatin and other platinum drugs. In summary, we uncovered AMBRA1 as a potential biomarker of response to platinum-based therapies in OSCCs.
Authors
- Mariana Yáñez-Bartolomé (ORCID: https://orcid.org/0000-0002-1218-7875)
- Ana Sastre-Perona (ORCID: https://orcid.org/0000-0002-4502-3025)
- Lucía Acero-Riaguas (ORCID: https://orcid.org/0000-0001-8101-5412)
- Beatriz Castelo (ORCID: https://orcid.org/0000-0002-4759-5035)
- Iván López-García
- Alejandro San Lorenzo-Vaquero
- Irene Posse-Alonso
- Catalina Berca
- César Pérez-Brotóns
Institutions
- Hospital Universitario La Paz (ES)
- Hospital La Paz Institute for Health Research (ES)
- Centre for Biomedical Network Research on Rare Diseases (ES)
- Instituto de Investigación de Enfermedades Raras (ES)
- Universidad Autónoma de Madrid (ES)
Publication Details
- Journal
- iScience
- Published
- 2026-07-27
- DOI
- https://doi.org/10.1016/j.isci.2026.116959
- Primary Topic
- PARP inhibition in cancer therapy
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Worldwide Cancer Research
- Comunidad de Madrid
- Fundación Científica Asociación Española Contra el Cáncer
- Instituto de Salud Carlos III