黑色素瘤
组织微阵列
黑素皮质素1受体
医学
免疫组织化学
肿瘤科
转移
生物标志物
内科学
病理
癌症
癌症研究
表型
生物
生物化学
基因
作者
David Su,Dijana Djureinovic,David A. Schoenfeld,Bernadette Marquez‐Nostra,Kelly Olino,Lucia B. Jilaveanu,Harriet M. Kluger
出处
期刊:JCO precision oncology
[American Society of Clinical Oncology]
日期:2024-04-01
卷期号: (8)
被引量:2
摘要
PURPOSE 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 patients with melanoma, yet large studies investigating the rate and degree of MC1R expression in primary and metastatic human melanoma tissue are lacking. METHODS 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. RESULTS 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 and ulcerated lesions and was associated with shorter survival in primary and metastatic tumors. On multivariable analysis, Breslow thickness, male sex, and chronic sun exposure were independent predictors of worse overall survival in the primary melanoma cohort. CONCLUSION 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.
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