Supplementary Data from Src-Dependent DBL Family Members Drive Resistance to Vemurafenib in Human Melanoma

Feddersen, Charlotte R.; Schillo, Jacob L.; Varzavand, Afshin; Vaughn, Hayley R.; Wadsworth, Lexy S.; Voigt, Andrew P.; Zhu, Eliot Y.; Jennings, Brooke M.; Mullen, Sarah A.; Bobera, Jeremy; Riordan, Jesse D.; Stipp, Christopher S.; Dupuy, Adam J.

doi:10.1158/0008-5472.22420994.v1

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Supplementary Data from Src-Dependent DBL Family Members Drive Resistance to Vemurafenib in Human Melanoma

journal contribution

posted on 2023-03-31, 02:23 authored by Charlotte R. Feddersen, Jacob L. Schillo, Afshin Varzavand, Hayley R. Vaughn, Lexy S. Wadsworth, Andrew P. Voigt, Eliot Y. Zhu, Brooke M. Jennings, Sarah A. Mullen, Jeremy Bobera, Jesse D. Riordan, Christopher S. Stipp, Adam J. Dupuy

Supplemental figures showing more detailed analysis of the genetic screen results (S1-S3), additional experiments showing biological validation of major candidate genes (S4-S7), and characterization of spontaneous Vemurafenib resistance in A375 cells (S8).

History

ARTICLE ABSTRACT

The use of selective BRAF inhibitors (BRAFi) has produced remarkable outcomes for patients with advanced cutaneous melanoma harboring a BRAFV600E mutation. Unfortunately, the majority of patients eventually develop drug-resistant disease. We employed a genetic screening approach to identify gain-of-function mechanisms of BRAFi resistance in two independent melanoma cell lines. Our screens identified both known and unappreciated drivers of BRAFi resistance, including multiple members of the DBL family. Mechanistic studies identified a DBL/RAC1/PAK signaling axis capable of driving resistance to both current and next-generation BRAFis. However, we show that the SRC inhibitor, saracatinib, can block the DBL-driven resistance. Our work highlights the utility of our straightforward genetic screening method in identifying new drug combinations to combat acquired BRAFi resistance. A simple, rapid, and flexible genetic screening approach identifies genes that drive resistance to MAPK inhibitors when overexpressed in human melanoma cells.