Sustained Adrenergic Signaling Promotes Intratumoral Innervation through BDNF Induction

Cancer Res. 2018 Jun 15;78(12):3233-3242. doi: 10.1158/0008-5472.CAN-16-1701. Epub 2018 Apr 16.

Abstract

Mounting clinical and preclinical evidence supports a key role for sustained adrenergic signaling in the tumor microenvironment as a driver of tumor growth and progression. However, the mechanisms by which adrenergic neurotransmitters are delivered to the tumor microenvironment are not well understood. Here we present evidence for a feed-forward loop whereby adrenergic signaling leads to increased tumoral innervation. In response to catecholamines, tumor cells produced brain-derived neurotrophic factor (BDNF) in an ADRB3/cAMP/Epac/JNK-dependent manner. Elevated BDNF levels in the tumor microenvironment increased innervation by signaling through host neurotrophic receptor tyrosine kinase 2 receptors. In patients with cancer, high tumor nerve counts were significantly associated with increased BDNF and norepinephrine levels and decreased overall survival. Collectively, these data describe a novel pathway for tumor innervation, with resultant biological and clinical implications.Significance: Sustained adrenergic signaling promotes tumor growth and metastasis through BDNF-mediated tumoral innervation. Cancer Res; 78(12); 3233-42. ©2018 AACR.

Publication types

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

MeSH terms

  • Animals
  • Brain-Derived Neurotrophic Factor / metabolism*
  • Cell Line, Tumor
  • Cyclic AMP / metabolism
  • Feedback, Physiological*
  • Female
  • Guanine Nucleotide Exchange Factors / metabolism
  • Humans
  • Membrane Glycoproteins / metabolism
  • Mice
  • Neoplasms / mortality
  • Neoplasms / pathology*
  • Norepinephrine / metabolism*
  • Peripheral Nerves / metabolism
  • Peripheral Nerves / pathology
  • Receptor, trkB / metabolism
  • Receptors, Adrenergic, beta-3 / metabolism*
  • Signal Transduction
  • Tumor Microenvironment / physiology
  • Xenograft Model Antitumor Assays

Substances

  • ADRB3 protein, human
  • Brain-Derived Neurotrophic Factor
  • Guanine Nucleotide Exchange Factors
  • Membrane Glycoproteins
  • RAPGEF3 protein, human
  • Receptors, Adrenergic, beta-3
  • BDNF protein, human
  • Cyclic AMP
  • Receptor, trkB
  • tropomyosin-related kinase-B, human
  • Norepinephrine