4.8 Article

Sustained Adrenergic Signaling Promotes Intratumoral Innervation through BDNF Induction

Journal

CANCER RESEARCH
Volume 78, Issue 12, Pages 3233-3242

Publisher

AMER ASSOC CANCER RESEARCH
DOI: 10.1158/0008-5472.CAN-16-1701

Keywords

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Categories

Funding

  1. NIGMS [P20GM103475]
  2. Puerto Rico Science, Technology and Research Trust
  3. NCI [U54CA163071, U54CA163068, G12MD007579]
  4. CPRIT Graduate Scholar Fellowship [RP140106]
  5. NIH T32 Training Grant [CA101642]
  6. NIH [CA140933, CA193249, CA109298, P50 CA217685, R35 CA209904, P50CA098258, CA016672, U54CA96300, U54CA96297]
  7. Ovarian Cancer Research Fund, Inc.
  8. Cancer Prevention Research Institute of Texas [RP101502, RP101489]
  9. NIH grant, Area 2 [U19CA148127]
  10. Ovarian Cancer Research Fund Program Project Development Grant
  11. Frank McGraw Memorial Chair in Cancer Research
  12. American Cancer Society Research Professor Award
  13. Blanton-Davis Ovarian Cancer Research Program

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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. (C) 2018 AACR.

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