Concurrent SOS1 and MEK suppression inhibits signaling and growth of NF1-null melanoma

Cell Rep Med. 2024 Nov 19;5(11):101818. doi: 10.1016/j.xcrm.2024.101818. Epub 2024 Nov 1.

Abstract

Neurofibromin (NF1) is a negative regulator of RAS signaling, frequently mutated in cancer. NF1-mutant melanoma is a highly malignant tumor for which targeted therapies are lacking. Here, we use biochemical and pharmacological assays on patient-derived models and isogenic cell lines to identify potential pharmacologic targets, revealing that NF1-null melanomas are dependent on RAS activation and that MEK inhibition relieves ERK-dependent negative feedback, increasing RAS signaling. MEK inhibition with avutometinib abrogates the adaptive rebound in ERK signaling, but the antitumor effects are limited. However, concurrent inhibition of MEK and SOS1 abrogates ERK activation, induces cell death, and suppresses tumor growth. In contrast to the NF1-deficient setting, concurrent SOS1 and SOS2 depletion is required to completely inhibit RAS signaling in NF1 wild-type cells. In sum, our data provide a mechanistic rationale for enhancing the therapeutic efficacy of MEK inhibitors by exploiting the lower residual SOS activity in NF1-null tumor cells.

Keywords: MEK inhibition; NF1; SOS1 inhibition; combination therapy; melanoma.

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Humans
  • MAP Kinase Signaling System / drug effects
  • Melanoma* / drug therapy
  • Melanoma* / genetics
  • Melanoma* / metabolism
  • Melanoma* / pathology
  • Mice
  • Mitogen-Activated Protein Kinase Kinases / antagonists & inhibitors
  • Mitogen-Activated Protein Kinase Kinases / metabolism
  • Neurofibromin 1* / genetics
  • Neurofibromin 1* / metabolism
  • Protein Kinase Inhibitors / pharmacology
  • SOS1 Protein* / genetics
  • SOS1 Protein* / metabolism
  • Signal Transduction / drug effects

Substances

  • Neurofibromin 1
  • SOS1 Protein
  • NF1 protein, human
  • Protein Kinase Inhibitors
  • SOS1 protein, human
  • Mitogen-Activated Protein Kinase Kinases