189P An image-based deep learning prediction model for characterization of the drug tolerant persister cell state
Targeted therapies improve the clinical outcome of cancer treatment. However, in solid tumors a cancer cell subpopulation survives during initial therapy and evolves into drug tolerant persister cells (DTPs) that maintain a residual disease reservoir. Residual disease contributes to lethal tumor progression; identifying and eliminating DTPs could benefit future treatment paradigms. We have shown that Hippo pathway effector Yes Associated Protein-1 (YAP1), a transcriptional co-regulator, is activated in oncogene-driven cancers in response to targeted therapy and maintains the DTP phenotype.
Authors
- Trever G. Bivona (ORCID: https://orcid.org/0000-0001-5734-4128)
- Larry G. Kerr
- Lauren Čech (ORCID: https://orcid.org/0000-0002-3621-4129)
- Wen‐Jeng Wu (ORCID: https://orcid.org/0000-0002-9691-7416)
- Victor Olivas
- Asif Zaman (ORCID: https://orcid.org/0000-0002-8411-6339)
Institutions
- University of California, San Francisco (US)
- UCSF Helen Diller Family Comprehensive Cancer Center (US)
Publication Details
- Journal
- Annals of Oncology
- Published
- 2024-09-01
- DOI
- https://doi.org/10.1016/j.annonc.2024.08.2194
- Primary Topic
- Computational Drug Discovery Methods
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Science Foundation
- University of California
- Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco