Abstract

Malignant melanoma, one of the most aggressive human malignancies, is responsible for 80% of skin cancer deaths. Whilst early detection of disease progression or metastasis can improve patient survival, this remains a challenge due to the lack of reliable biomarkers. Importantly, these clinical challenges are not unique to humans, as melanoma affects many other species, including companion animals, such as the dog and horse. Extracellular vesicles (EVs) are tiny nanoparticles involved in cell-to-cell communication. Several protein and genomic EV markers have been described in the literature, as well as a wide variety of methods for isolating EVs from body fluids. As such, they may be valuable biomarkers in cancer and may address some clinical challenges in the management melanoma. This review aimed to explore the translational applications of EVs as biomarkers in melanoma, as well as their role in the clinical setting in humans and animals. A summary of melanoma-specific protein and genomic EV markers is presented, followed by a discussion of the role EVs in monitoring disease progression and treatment response. Finally, herein, we reviewed the advantages and disadvantages of methods utilised to isolate EVs from bodily fluids in melanoma patients (human and animals) and describe some of the challenges that will need to be addressed before EVs can be introduced in the clinical setting.

Highlights

  • Malignant melanoma, one of the most aggressive human malignancies, is responsible for 80% of skin cancer-associated deaths [1]

  • This review aimed to explore the translational applications of Extracellular vesicles (EVs) as biomarkers in melanoma (Figure 1), and their role in the clinical setting in humans and animals

  • In vitro and murine studies have demonstrated an increased secretion of miR-211-5p containing EVs as a response to treatment with BRAF inhibition with dabrafenib [96]. This suggests that EVs can be used to monitor tumour stress response or injury. These findings argue well for clinical application in humans, and it has been reported that human patients undergoing treatment with chemotherapy may have lower levels of caveolin-1-related EVs [53]

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Summary

Introduction

One of the most aggressive human malignancies, is responsible for 80% of skin cancer-associated deaths [1]. A Breslow thickness of

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