Calcitonin Related Polypeptide Alpha Mediates Oral Cancer Pain

Author:

Tu Nguyen Huu1ORCID,Inoue Kenji1,Lewis Parker K.2,Khan Ammar1,Hwang Jun Hyeong1,Chokshi Varun1,Dabovic Branka Brukner3,Selvaraj Shanmugapriya3,Bhattacharya Aditi1ORCID,Dubeykovskaya Zinaida1,Pinkerton Nathalie M.2,Bunnett Nigel W.456,Loomis Cynthia A.3,Albertson Donna G.16ORCID,Schmidt Brian L.156

Affiliation:

1. Department of Oral and Maxillofacial Surgery, Translational Research Center, New York University College of Dentistry, New York, NY 10010, USA

2. Department of Chemical and Biomolecular Engineering, New York University Tandon School of Engineering, New York, NY 10010, USA

3. Department of Pathology, NYU Langone Health, New York, NY 10010, USA

4. Department of Molecular Pathobiology, New York University College of Dentistry, New York, NY 10010, USA

5. Department of Neuroscience and Physiology, Neuroscience Institute, NYU Langone Health, New York, NY 10016, USA

6. NYU Pain Research Center, New York University College of Dentistry, New York, NY 10010, USA

Abstract

Oral cancer patients suffer pain at the site of the cancer. Calcitonin gene related polypeptide (CGRP), a neuropeptide expressed by a subset of primary afferent neurons, promotes oral cancer growth. CGRP also mediates trigeminal pain (migraine) and neurogenic inflammation. The contribution of CGRP to oral cancer pain is investigated in the present study. The findings demonstrate that CGRP-immunoreactive (-ir) neurons and neurites innervate orthotopic oral cancer xenograft tumors in mice. Cancer increases anterograde transport of CGRP in axons innervating the tumor, supporting neurogenic secretion as the source of CGRP in the oral cancer microenvironment. CGRP antagonism reverses oral cancer nociception in preclinical oral cancer pain models. Single-cell RNA-sequencing is used to identify cell types in the cancer microenvironment expressing the CGRP receptor components, receptor activity modifying protein 1 Ramp1 and calcitonin receptor like receptor (CLR, encoded by Calcrl). Ramp1 and Calcrl transcripts are detected in cells expressing marker genes for Schwann cells, endothelial cells, fibroblasts and immune cells. Ramp1 and Calcrl transcripts are more frequently detected in cells expressing fibroblast and immune cell markers. This work identifies CGRP as mediator of oral cancer pain and suggests the antagonism of CGRP to alleviate oral cancer pain.

Funder

National Institutes of Health

Department of Defense

NYU Langone Health Experimental Pathology Research Laboratory

NYU Langone Health Genome Technology Center

NCI Cancer Center Support Grant

NIH Shared Instrumentation Grant

Publisher

MDPI AG

Subject

General Medicine

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