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PRAME Updated: Diagnostic, Prognostic, and Therapeutic Role in Skin Cancer.
Cassalia, Fortunato; Danese, Andrea; Tudurachi, Ina; Federico, Serena; Zambello, Anna; Guidotti, Alessia; Franceschin, Ludovica; Bolzon, Anna; Naldi, Luigi; Belloni Fortina, Anna.
Afiliação
  • Cassalia F; Dermatology Unit, Department of Medicine (DIMED), University of Padua, 35121 Padua, Italy.
  • Danese A; Dermatology Unit, Department of Integrated Medical and General Activity, University of Verona, 37100 Verona, Italy.
  • Tudurachi I; Dermatology Unit, Department of Medicine (DIMED), University of Padua, 35121 Padua, Italy.
  • Federico S; Dermatology Unit, University of Magna Graecia, 88100 Catanzaro, Italy.
  • Zambello A; Dermatology Unit, Department of Medicine (DIMED), University of Padua, 35121 Padua, Italy.
  • Guidotti A; Dermatology Unit, Department of Medicine (DIMED), University of Padua, 35121 Padua, Italy.
  • Franceschin L; Dermatology Unit, Department of Medicine (DIMED), University of Padua, 35121 Padua, Italy.
  • Bolzon A; Dermatology Unit, Department of Medicine (DIMED), University of Padua, 35121 Padua, Italy.
  • Naldi L; Department of Dermatology, Ospedale San Bortolo, 36100 Vicenza, Italy.
  • Belloni Fortina A; Centro Studi Gruppo Italiano Studi Epidemiologici in Dermatologia (GISED), 24121 Bergamo, Italy.
Int J Mol Sci ; 25(3)2024 Jan 27.
Article em En | MEDLINE | ID: mdl-38338862
ABSTRACT
Preferentially Expressed Antigen in Melanoma (PRAME), a member of the cancer/testis antigen family, is central to the field of skin cancer diagnostics and therapeutics. As a nuclear receptor and transcriptional regulator, PRAME plays a critical role in inhibiting retinoic acid signalling, which is essential for cell differentiation and proliferation. Its aberrant overexpression in various malignancies, particularly cutaneous melanoma, is associated with more aggressive tumour phenotypes, positioning PRAME as both a diagnostic and prognostic marker. In melanoma, PRAME is typically highly expressed, in contrast to its weak or absent expression in benign nevi, thereby improving the accuracy of differential diagnoses. The diagnostic value of PRAME extends to various lesions. It is significantly expressed in uveal melanoma, correlating to an increased risk of metastasis. In acral melanomas, especially those with histopathological ambiguity, PRAME helps to improve diagnostic accuracy. However, its expression in spitzoid and ungual melanocytic lesions is inconsistent and requires a comprehensive approach for an accurate assessment. In soft tissue sarcomas, PRAME may be particularly helpful in differentiating melanoma from clear cell sarcoma, an important distinction due to their similar histological appearance but different treatment approaches and prognosis, or in detecting dedifferentiated and undifferentiated melanomas. In non-melanoma skin cancers such as basal cell carcinoma, squamous cell carcinoma, and Merkel cell carcinoma, the variable expression of PRAME can lead to diagnostic complexity. Despite these challenges, the potential of PRAME as a therapeutic target in melanoma is significant. Emerging immunotherapies, including T-cell-based therapies and vaccines targeting PRAME, are being investigated to exploit its cancer-specific expression. Ongoing research into the molecular role and mechanism of action of PRAME in skin cancer continues to open new avenues in both diagnostics and therapeutics, with the potential to transform the management of melanoma and related skin cancers.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Melanoma / Antígenos de Neoplasias Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans / Male Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Melanoma / Antígenos de Neoplasias Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans / Male Idioma: En Ano de publicação: 2024 Tipo de documento: Article