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The role of macrophage migration inhibitory factor family and CD74 in the pathogenesis of melanoma.
- Source :
-
Experimental dermatology [Exp Dermatol] 2024 Jun; Vol. 33 (6), pp. e15122. - Publication Year :
- 2024
-
Abstract
- Melanoma is an aggressive tumour with poor prognosis that arises from the malignant transformation of melanocytes. Over the past few decades, intense research into the pathogenesis of melanoma has led to the development of BRAF and immune checkpoint inhibitors, including antibodies against programmed cell death protein 1 (PD-1) and cytotoxic T lymphocyte-associated protein 4 (CTLA-4), which have shown clinically significant efficacy. However, some tumours do not respond to these therapies initially or become treatment resistant. Most melanoma tissues appear to possess biological characteristics that allow them to evade these treatments, and identifying these characteristics is one of the major challenges facing cancer researchers. One such characteristic that has recently gained attention is the role of macrophage migration inhibitory factor (MIF) and its receptor CD74. This review outlines the cellular and molecular functions of CD74, MIF and their family of proteins. We then review their roles in tumours based on previous reports, highlight their pathological significance in melanoma and discuss their potential as therapeutic targets.<br /> (© 2024 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.)
- Subjects :
- Humans
Skin Neoplasms metabolism
Skin Neoplasms pathology
Skin Neoplasms etiology
Animals
Melanoma metabolism
Melanoma pathology
Melanoma etiology
Macrophage Migration-Inhibitory Factors metabolism
Antigens, Differentiation, B-Lymphocyte metabolism
Histocompatibility Antigens Class II metabolism
Intramolecular Oxidoreductases metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1600-0625
- Volume :
- 33
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Experimental dermatology
- Publication Type :
- Academic Journal
- Accession number :
- 38884501
- Full Text :
- https://doi.org/10.1111/exd.15122