Melanocortin 1 receptor (MC1R) expression as a marker of progression in melanoma.

MC1R diagnostic markers progression markers theranostics therapeutic targets

Journal

Research square
Titre abrégé: Res Sq
Pays: United States
ID NLM: 101768035

Informations de publication

Date de publication:
19 Sep 2023
Historique:
medline: 4 10 2023
pubmed: 4 10 2023
entrez: 4 10 2023
Statut: epublish

Résumé

Melanocortin-1 receptor (MC1R) plays a critical role in human pigmentation and DNA repair mechanisms. MC1R-targeting agents are being investigated in clinical trials in melanoma patients, yet large studies investigating the rate and degree of MC1R expression in primary and metastatic human melanoma tissue are lacking. Using tissue microarrays containing three large cohorts of 225 cases of benign nevi, 189 with primary melanoma, and 271 with metastatic melanoma, we applied quantitative immunofluorescence and immunohistochemistry to comprehensively study MC1R protein expression. We show a stepwise elevation of MC1R expression in different stages of melanoma progression (nevi, primary, metastasis). Higher MC1R expression was seen in deeper (>1 mm) primary lesions, ulcerated lesions, and mucosal melanomas compared to cutaneous melanomas and was associated with shorter survival in primary and metastatic tumors. On multi-variable analysis, Breslow thickness, ulceration, male sex, and chronic sun exposure were independent predictors of worse overall survival in the primary melanoma cohort. In the metastatic melanoma cohort, MC1R expression and mucosal melanomas were independent predictors of inferior overall survival. Our data suggest that MC1R might be a valuable drug target in aggressive melanoma. Additional studies are warranted to determine its functional significance in melanoma progression and its utility as a predictive biomarker in patients receiving MC1R-directed therapies.

Identifiants

pubmed: 37790306
doi: 10.21203/rs.3.rs-3314825/v1
pmc: PMC10543287
pii:
doi:

Types de publication

Preprint

Langues

eng

Déclaration de conflit d'intérêts

Competing interests HK has received consulting fees from Iovance, Immunocore, Celldex, Merck, Elevate Bio, Instil Bio, Bristol-Myers Squibb, Clinigen, Shionogi, Chemocentryx, Calithera, Signatero, Gigagen, GI Reviewers, all outside of the submitted work. HK has also received research grant funding (to Yale University) from Merck, Bristol-Myers Squibb and Apexigen. DD reports stock ownership in Atlas Antibodies. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Auteurs

David Su (D)

Division of Surgical Oncology, Yale University School of Medicine, New Haven, CT.

Dijana Djureinovic (D)

Division of Medical Oncology, Yale University School of Medicine, New Haven, CT.

David Schoenfeld (D)

Division of Medical Oncology, Yale University School of Medicine, New Haven, CT.

Bernadette Marquez-Nostra (B)

Department of Radiology, Division of Advanced Medical Imaging Research, University of Alabama at Birmingham, Birmingham, AL.

Kelly Olino (K)

Division of Surgical Oncology, Yale University School of Medicine, New Haven, CT.

Lucia Jilaveanu (L)

Division of Medical Oncology, Yale University School of Medicine, New Haven, CT.

Harriet Kluger (H)

Division of Medical Oncology, Yale University School of Medicine, New Haven, CT.

Classifications MeSH