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- Potential to suppress tumor growth and cancer cell proliferation.
- Treatment with a synergistic combination of YAP/SOX2 inhibitor(s) that effectively induce cancer cell death and tumor growth arrest in YAP-dependent cancer cells
- Overcome SOX2-mediated resistance to YAP inhibitors in cancer cells through SOX2 inhibition
OVERVIEW
Georgetown University researchers discovered a potential drug treatment method whereby the YAP pathway is inhibited in YAP-dependent cancer cells with a synergistic combination of YAP/SOX2 inhibitor(s). This method counteracts cancer cell resistance to YAP inhibitors by opposing SOX2 upregulation, leading to cell death and growth arrest in cancer cells.
BACKGROUND
The activation of transcriptional co-activator yes-associated protein 1 (YAP) is critical for tumor initiation and progression. Although YAP inhibitors are effective to a certain extent, many cancer cells develop resistance to such treatments through a pathway involving the upregulation of SRY-Box Transcription Factor 2 (SOX2). Therefore, solutions with the ability to inhibit both YAP and SOX2 may prove helpful in treating YAP-dependent cancer.
Benefit
Method to counteract SOX2-mediated resistance to YAP inhibitors.
Market Application
Treatment or prevention of cancer, noncancerous tumors or lesions through the administration of YAP/SOX2 inhibitors.
Publications
US patent No. 17/636,735
A Yap-Myc-Sox2-p53 Regulatory Network Dictates Metabolic Homeostasis and Differentiation in Kras-Driven Pancreatic Ductal Adenocarcinomas (DOI: https://doi.org/10.1016/j.devcel.2019.07.022) (link: https://www.sciencedirect.com/science/article/pii/S1534580719306288)
YAP/TAZ Signaling and Resistance to Cancer Therapy (DOI: https://doi.org/10.1016/j.trecan.2019.02.010) (link: https://www.sciencedirect.com/science/article/abs/pii/S2405803319300287)
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