T Cell Immunoglobulin and Mucin Domain 3 (TIM-3) in Cutaneous Melanoma: A Narrative Review

Author:

Cazzato Gerardo1ORCID,Cascardi Eliano23ORCID,Colagrande Anna1ORCID,Lettini Teresa1ORCID,Filosa Alessandra4,Arezzo Francesca5,Lupo Carmelo6ORCID,Casatta Nadia6ORCID,Loizzi Vera5ORCID,Pellegrini Cristina7,Fargnoli Maria Concetta7ORCID,Maiorano Eugenio1ORCID,Cicco Gerolamo1,Tamma Roberto8ORCID,Ingravallo Giuseppe1ORCID

Affiliation:

1. Section of Molecular Pathology, Department of Precision and Regenerative Medicine and Ionian Area (DiMePRe-J), University of Bari “Aldo Moro”, 70124 Bari, Italy

2. Department of Medical Sciences, University of Turin, 10124 Turin, Italy

3. Pathology Unit, FPO-IRCCS Candiolo Cancer Institute, Str. Provinciale 142 lm 3.95, 10060 Candiolo, Italy

4. Pathology Department, “A. Murri” Hospital-ASUR Marche, Aree Vaste n. 4 and 5, 63900 Fermo, Italy

5. Obstetrics and Gynecology Unit, IRCSS Giovanni Paolo II, 70124 Bari, Italy

6. Innovation Department, Diapath S.p.A., Via Savoldini n.71, 24057 Martinengo, Italy

7. Dermatology, Department of Biotechnological and Applied Clinical Sciences, University of L’Aquila, 67100 L’Aquila, Italy

8. Department of Translational Biomedicine and Neurosciences, Section of Human Anatomy and Histology, School of Medicine and Surgery, University of Bari “Aldo Moro”, Piazza Giulio Cesare, 11 Polyclinic, 70124 Bari, Italy

Abstract

T cell immunoglobulin and mucin domain 3 (TIM-3) is an inhibitory immunocheckpoint that belongs to the TIM gene family. Monney et al. first discovered it about 20 years ago and linked it to some autoimmune diseases; subsequent studies have revealed that some tumours, including melanoma, have the capacity to produce inhibitory ligands that bind to these receptor checkpoints on tumour-specific immune cells. We conducted a literature search using PubMed, Web of Science (WoS), Scopus, Google Scholar, and Cochrane, searching for the following keywords: “T cell immunoglobulin and mucin-domain containing-3”, “TIM-3” and/or “Immunocheckpoint inhibitors” in combination with “malignant melanoma” or “human malignant melanoma” or “cutaneous melanoma”. The literature search initially turned up 117 documents, 23 of which were duplicates. After verifying eligibility and inclusion criteria, 17 publications were ultimately included. A growing body of scientific evidence considers TIM-3 a valid inhibitory immuno-checkpoint with a very interesting potential in the field of melanoma. However, other recent studies have discovered new roles for TIM-3 that seem almost to contradict previous findings in this regard. All this demonstrates how common and valid the concept of ‘pleiotropism’ is in the TME field, in that the same molecule can behave completely or partially differently depending on the cell type considered or on temporary conditions. Further studies, large case series, and a special focus on the immunophenotype of TIM-3 are absolutely necessary in order to explore this highly promising topic in the near future.

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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