CGRP signaling links tumor-associated pain to immune evasion in oral squamous cell carcinoma
Peripheral sensory nerves are thought to play a role in solid tumor growth, particularly in oral squamous cell carcinoma (OSCC); however, the link between pain and immunosuppression remains unresolved. Here, we find an inverse relationship between OSCC-associated pain by way of calcitonin gene-related peptide (CGRP)-expressing nerves and tumor-associated immunity in patients with OSCC. Bulk RNA sequencing of tumor-innervating sensory neurons from syngeneic mouse models of OSCC shows differential regulation of genes associated with excitability, neurotransmission, and axonal sprouting. Using a gain-of-function approach by persistently stimulating peptidergic afferents, we show that sensory neurons support the growth of oral tongue tumors and limit the activation of an effective anti-tumor immune response via efferent CGRP release. Loss-of-function approaches, such as local ablation of nociceptive nerves or systemic CGRP receptor antagonism, slow tumor growth and improve anti-tumor immunity. Targeting CGRP may serve as a potential therapeutic strategy in OSCC to reduce pain and improve therapeutic response.
Authors
- Megan A. Atherton (ORCID: https://orcid.org/0000-0001-6199-4131)
- Nicole N. Scheff (ORCID: https://orcid.org/0000-0002-5587-4990)
- Sébastien Talbot (ORCID: https://orcid.org/0000-0001-9932-7174)
- Lisa A. McIlvried (ORCID: https://orcid.org/0000-0002-2030-1316)
- Marci L. Nilsen (ORCID: https://orcid.org/0000-0002-5888-668X)
- Morgan Ottley
- Rachel S. Krane
- Kathryn T. Eskew
- Maryam Ahmadi
- Tian LeGrande
- Amin Reza Nikpoor
- Diana Bell
- Andre A. Martel Matos
Institutions
- University of Pittsburgh (US)
- Queen's University (CA)
- UPMC Hillman Cancer Center (US)
- University of Pittsburgh Medical Center (US)
Publication Details
- Journal
- Cell Reports
- Published
- 2026-02-01
- DOI
- https://doi.org/10.1016/j.celrep.2026.116994
- Primary Topic
- Cancer, Stress, Anesthesia, and Immune Response
- Type
- article
- Field-Weighted Citation Impact
- 0.00