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Research on Diagnostics, Pathogenesis and Novel Therapeutic Tools in Melanoma

A special issue of International Journal of Molecular Sciences (ISSN 1422-0067). This special issue belongs to the section "Molecular Oncology".

Deadline for manuscript submissions: closed (30 April 2024) | Viewed by 594

Special Issue Editor

Dermatology Section, Department of Experimental, Diagnostic and Specialty Medicine, DIMES, University of Bologna, 40138 Bologna, Italy
Interests: melanoma; squamous cell carcinoma; Merkel cell carcinoma; basal cell carcinoma; mucosal neoplasms; environmental factors; genetics; molecular alterations; risk factors; drugs
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Special Issue Information

Dear Colleagues,

Melanoma is a malignant tumor arising from the neoplastic transformation of cutaneous and/or mucosal melanocytes. In the field of dermatological oncology, melanoma due to its metastatic potential, although it represents only 4% of skin tumors, is responsible for 80% of deaths from skin cancer. The etiology of melanoma is influenced by both genetic susceptibility and environmental factors. Risk factors include the presence of common and atypical nevi, light skin type, UV radiation exposure patterns, family or personal history of melanoma, non-melanoma skin tumors, and premalignant skin lesions. However, the exact pathogenetic mechanism is still to be clarified. The primary susceptibility genes in melanoma, especially in cases of familial or multiple melanomas, are CDKN2A and CDK4, which are tumor suppressor genes. In sporadic melanoma cases, mutations are frequently found in genes encoding protein kinases related to MAPK and PI-3K/AKT signaling pathways, as well as genes involved in cell cycle and apoptosis, such as BRAF, RAS, NF1, KIT, PTEN/PI3K/AKT, TERT, GNAAQ/GNA11, BAP1, MITF, and P53. Recent scientific research has identified a growing number of other genes potentially involved in melanoma susceptibility. The choice of which genes to include in melanoma screening is still a subject of study and discussion, reflecting the ongoing development in our understanding of this complex condition.

In recent years, great advancements have been achieved in the early diagnosis of this tumor combining (video)dermatoscopy first with reflectance confocal microscopy (RCM) and more recently, with line-field confocal optical coherence tomography (LC-OCT), a technology whose potential described in the current literature is limited but gradually growing to date.

The focus of this Special Issue is on the research of novel experimental therapies and studies highlighting new therapies adopted in clinical practices, their evolution, and their effects on improving prognosis. Novel investigations on alternative therapeutic strategies in order to overcome drug resistance will be particularly appreciated, as will findings aiming to improve prevention and early diagnosis of malignant melanoma.

Dr. Emi Dika
Guest Editor

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Keywords

  • melanoma
  • LC-OCT
  • early diagnosis
  • differential diagnosis
  • genetics
  • genes
  • markers

Published Papers (1 paper)

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Research

14 pages, 3273 KiB  
Article
In Vitro and In Vivo Studies of Melanoma Cell Migration by Antagonistic Mimetics of Adhesion Molecule L1CAM
by Stefano Vito Boccadamo Pompili, Sophia Fanzini, Melitta Schachner and Suzie Chen
Int. J. Mol. Sci. 2024, 25(9), 4811; https://doi.org/10.3390/ijms25094811 - 28 Apr 2024
Viewed by 280
Abstract
Melanoma, the deadliest type of skin cancer, has a high propensity to metastasize to other organs, including the brain, lymph nodes, lungs, and bones. While progress has been made in managing melanoma with targeted and immune therapies, many patients do not benefit from [...] Read more.
Melanoma, the deadliest type of skin cancer, has a high propensity to metastasize to other organs, including the brain, lymph nodes, lungs, and bones. While progress has been made in managing melanoma with targeted and immune therapies, many patients do not benefit from these current treatment modalities. Tumor cell migration is the initial step for invasion and metastasis. A better understanding of the molecular mechanisms underlying metastasis is crucial for developing therapeutic strategies for metastatic diseases, including melanoma. The cell adhesion molecule L1CAM (CD171, in short L1) is upregulated in many human cancers, enhancing tumor cell migration. Earlier studies showed that the small-molecule antagonistic mimetics of L1 suppress glioblastoma cell migration in vitro. This study aims to evaluate if L1 mimetic antagonists can inhibit melanoma cell migration in vitro and in vivo. We showed that two antagonistic mimetics of L1, anagrelide and 2-hydroxy-5-fluoropyrimidine (2H5F), reduced melanoma cell migration in vitro. In in vivo allograft studies, only 2H5F-treated female mice showed a decrease in tumor volume. Full article
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