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Data from Sustained Adrenergic Signaling Promotes Intratumoral Innervation through BDNF Induction

Authors :
Anil K. Sood
Mariella De Biasi
Susan K. Lutgendorf
Steve W. Cole
Gabriel Lopez-Berestein
Frank C. Marini
Stephen T.C. Wong
Prahlad T. Ram
Erika L. Spaeth
Vasudha Sehgal
Cristian Rodriguez-Aguayo
Lingegowda S. Mangala
Yu Kang
Myrthala Moreno-Smith
Justin Bottsford-Miller
Wei Hu
Morgan Taylor
Heather J. Dalton
Behrouz Zand
Hee Dong Han
Xiaoyun Xu
Sunila Pradeep
Sherry Y. Wu
Rebecca A. Previs
Rajesha Rupaimoole
Kshipra M. Gharpure
Monika Haemmerle
Danielle M. Herder
Merve Ozcan
Robert Dood
Tatiana Ortiz
Nouara C. Sadaoui
Archana S. Nagaraja
Guillermo N. Armaiz-Pena
Julie K. Allen
Publication Year :
2023
Publisher :
American Association for Cancer Research (AACR), 2023.

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.

Details

Database :
OpenAIRE
Accession number :
edsair.doi.dedup.....7ed3bdd54947735db8752aa11a065611
Full Text :
https://doi.org/10.1158/0008-5472.c.6509690.v1