Chemogenetic modulation of sensory neurons reveals their regulating role in melanoma progression

Acta Neuropathol Commun. 2021 Nov 16;9(1):183. doi: 10.1186/s40478-021-01273-9.

Abstract

Sensory neurons have recently emerged as components of the tumor microenvironment. Nevertheless, whether sensory neuronal activity is important for tumor progression remains unknown. Here we used Designer Receptors Exclusively Activated by a Designer Drug (DREADD) technology to inhibit or activate sensory neurons' firing within the melanoma tumor. Melanoma growth and angiogenesis were accelerated following inhibition of sensory neurons' activity and were reduced following overstimulation of these neurons. Sensory neuron-specific overactivation also induced a boost in the immune surveillance by increasing tumor-infiltrating anti-tumor lymphocytes, while reducing immune-suppressor cells. In humans, a retrospective in silico analysis of melanoma biopsies revealed that increased expression of sensory neurons-related genes within melanoma was associated with improved survival. These findings suggest that sensory innervations regulate melanoma progression, indicating that manipulation of sensory neurons' activity may provide a valuable tool to improve melanoma patients' outcomes.

Keywords: Chemogenetics; Melanoma; Neuronal activity; Sensory neurons; Tumor microenvironment.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Behavior, Animal / drug effects
  • Biopsy
  • Cell Line, Tumor
  • Computer Simulation
  • Disease Progression
  • Humans
  • Immunologic Surveillance
  • Lymphocytes / pathology
  • Melanoma / genetics*
  • Melanoma / pathology*
  • Melanoma, Experimental / genetics
  • Melanoma, Experimental / pathology
  • Mice
  • Mice, Transgenic
  • NAV1.8 Voltage-Gated Sodium Channel / genetics
  • Neovascularization, Pathologic / genetics
  • Neovascularization, Pathologic / pathology
  • Sensory Receptor Cells / metabolism
  • Sensory Receptor Cells / pathology*
  • Suppressor Factors, Immunologic
  • Tumor Microenvironment

Substances

  • NAV1.8 Voltage-Gated Sodium Channel
  • Scn10a protein, mouse
  • Suppressor Factors, Immunologic