Mokos Mislav, Prkačin Ivana, Gaćina Klara, Brkić Ana, Pondeljak Nives, Šitum Mirna
Department of Dermatology and Venereology, Sestre Milosrdnice University Hospital Center, 10000 Zagreb, Croatia.
School of Medicine, University of Split, 21000 Split, Croatia.
Biomedicines. 2025 Aug 15;13(8):1988. doi: 10.3390/biomedicines13081988.
Melanoma is one of the most aggressive types of skin cancer. Its diagnosis appears to be challenging due to morphological similarities to benign melanocytic lesions. Even though histopathological evaluation is the diagnostic gold standard, immunohistochemistry (IHC) proves to be useful in challenging cases. Preferentially Expressed Antigen in Melanoma (PRAME) has emerged as a promising diagnostic, prognostic, and therapeutic marker in melanoma. This review critically examines the role of PRAME across clinical domains. It presents an evaluation of PRAME's diagnostic utility in differentiating melanomas from benign nevi, its prognostic significance across melanoma subtypes, and therapeutic applications in emerging immunotherapy strategies. An extensive analysis of the current literature was conducted, with a focus on PRAME expression patterns in melanocytic lesions and various malignancies, along with its integration into IHC protocols and investigational therapies. PRAME demonstrates high specificity and sensitivity in distinguishing melanoma from benign melanocytic proliferations, particularly in challenging subtypes such as acral, mucosal, and spitzoid lesions. Its overexpression correlates with poor prognosis in numerous malignancies. Therapeutically, PRAME's HLA class I presentation enables T-cell-based targeting. Early-phase trials show promising results using PRAME-directed TCR therapies and bispecific ImmTAC agents. However, immune evasion mechanisms (i.e., heterogeneous antigen expression, immune suppression in the tumor microenvironment, and HLA downregulation) pose significant challenges to therapy. PRAME is a valuable biomarker for melanoma diagnosis and a promising target for immunotherapy. Its selective expression in malignancies supports its clinical utility in diagnostic precision, prognostic assessment, and precision oncology. Ongoing research aimed at overcoming immunological barriers will be essential for optimizing PRAME-directed therapies and establishing their place in the personalized management of melanoma.
黑色素瘤是最具侵袭性的皮肤癌类型之一。由于其在形态学上与良性黑素细胞病变相似,其诊断似乎具有挑战性。尽管组织病理学评估是诊断的金标准,但免疫组织化学(IHC)在具有挑战性的病例中被证明是有用的。黑色素瘤优先表达抗原(PRAME)已成为黑色素瘤中一种有前景的诊断、预后和治疗标志物。本综述批判性地研究了PRAME在各个临床领域的作用。它评估了PRAME在区分黑色素瘤与良性痣方面的诊断效用、其在黑色素瘤各亚型中的预后意义以及在新兴免疫治疗策略中的治疗应用。对当前文献进行了广泛分析,重点关注PRAME在黑素细胞病变和各种恶性肿瘤中的表达模式,以及其纳入免疫组织化学方案和研究性治疗。PRAME在区分黑色素瘤与良性黑素细胞增殖方面表现出高特异性和敏感性,特别是在肢端、黏膜和梭形细胞样病变等具有挑战性的亚型中。其过表达与多种恶性肿瘤的不良预后相关。在治疗方面,PRAME的HLA I类呈递能够实现基于T细胞的靶向。早期试验使用PRAME导向的TCR疗法和双特异性免疫衔接器(ImmTAC)药物显示出有前景的结果。然而,免疫逃逸机制(即异质性抗原表达、肿瘤微环境中的免疫抑制和HLA下调)对治疗构成了重大挑战。PRAME是黑色素瘤诊断的有价值生物标志物,也是免疫治疗的有前景靶点。其在恶性肿瘤中的选择性表达支持了其在诊断准确性、预后评估和精准肿瘤学中的临床效用。旨在克服免疫障碍的正在进行的研究对于优化PRAME导向的治疗并在黑色素瘤的个性化管理中确立其地位至关重要。