Chemokines as possible therapeutic targets in metastatic melanoma

Author:

Basson Charlise1ORCID,Serem June Cheptoo2ORCID,Bipath Priyesh1ORCID,Hlophe Yvette Nkondo1ORCID

Affiliation:

1. Department of Physiology, School of Medicine University of Pretoria Pretoria South Africa

2. Department of Anatomy, School of Medicine University of Pretoria Pretoria South Africa

Abstract

AbstractBackgroundCutaneous melanoma is a relentless form of cancer which continues to rise in incidence. Currently, cutaneous melanoma is the leading cause of skin cancer‐related mortality, which can mainly be attributed to its metastatic potential. The activation of chemokine axes is a major contributor to melanoma metastasis through its involvement in promoting tumour cell migration, proliferation, survival, and adhesion. This review will focus on the role of chemokines in melanoma and possible therapeutic strategies to alter chemokine activation and subsequently inhibit the activation of signalling cascades that may promote metastasis.MethodsA literature review was conducted to evaluate chemokines as possible therapeutic targets in metastatic melanoma.ResultsThe crosstalk between signalling pathways and immune responses in the melanoma microenvironment resembles a complex and dynamic system. Therefore, the involvement of governing chemokine axes in the promotion of cutaneous and metastatic melanoma demands a proper understanding of the tumour microenvironment in order to identify possible targets and develop appropriate treatments against melanoma.ConclusionEven though chemokine axes are regarded as promising therapeutic targets, it has become increasingly evident that chemokines can play a critical role in both tumour inhibition and promotion. The inhibition of chemokine axes to inhibit signalling cascades in target cells that regulate metastasis should, therefore, be carefully approached.

Funder

University of Pretoria

Publisher

Wiley

Subject

Cancer Research,Radiology, Nuclear Medicine and imaging,Oncology

Reference111 articles.

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