| Autor: |
Kasturee Jagirdar, Marie Portuallo, Matthew Wilhide, Waqar Ahmed, Meihan Wei, Bailey Robertson, Jeremy Bravo, Gretchen Alicea, Crystal Aguh, Min Xiao, Tetiana Godok, Dylan Fingerman, Gregory Brown, Meenhard Herlyn, Brian Guo, Eneda Toska, Daniel Zabransky, Bradley Wubbenhorst, Katherine Nathanson, Hongkai Ji, Qin Liu, Vito Rebecca |
| Rok vydání: |
2022 |
| DOI: |
10.21203/rs.3.rs-2023316/v1 |
| Popis: |
Patients with metastatic acral lentiginous melanoma (ALM) suffer worse outcomes relative to patients with other forms of cutaneous melanoma (CM), and do not benefit as well to approved melanoma therapies. Identification of cyclin-dependent kinase 4 and 6 (CDK4/6) pathway gene alterations in >60% of ALMs has led to clinical trials of the CDK4/6 inhibitor (CDK4i/6i) palbociclib for ALM; however, median progression free survival with CDK4i/6i treatment was only 2.2 months, suggesting existence of resistance mechanisms. Therapy resistance in ALM remains poorly understood; here we report hyperactivation of MAPK signaling and elevated cyclin D1 expression are a unified mechanism of both intrinsic and acquired CDK4i/6i resistance. MEK or ERK inhibition increases CDK4i/6i efficacy in a patient-derived xenograft (PDX) models of ALM and promotes a defective DNA repair, cell cycle arrested and apoptotic program. Concurrent targeting of the MAPK pathway and CDK4/6 represents a new approach to improve outcomes for patients with advanced ALM. |
| Databáze: |
OpenAIRE |
| Externí odkaz: |
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