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Chemokines as possible therapeutic targets in metastatic melanoma

BACKGROUND: Cutaneous 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...

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Autores principales: Basson, Charlise, Serem, June Cheptoo, Bipath, Priyesh, Hlophe, Yvette Nkondo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10358257/
https://www.ncbi.nlm.nih.gov/pubmed/37170733
http://dx.doi.org/10.1002/cam4.6055
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author Basson, Charlise
Serem, June Cheptoo
Bipath, Priyesh
Hlophe, Yvette Nkondo
author_facet Basson, Charlise
Serem, June Cheptoo
Bipath, Priyesh
Hlophe, Yvette Nkondo
author_sort Basson, Charlise
collection PubMed
description BACKGROUND: Cutaneous 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. METHODS: A literature review was conducted to evaluate chemokines as possible therapeutic targets in metastatic melanoma. RESULTS: The 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. CONCLUSION: Even 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.
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spelling pubmed-103582572023-07-21 Chemokines as possible therapeutic targets in metastatic melanoma Basson, Charlise Serem, June Cheptoo Bipath, Priyesh Hlophe, Yvette Nkondo Cancer Med REVIEWS BACKGROUND: Cutaneous 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. METHODS: A literature review was conducted to evaluate chemokines as possible therapeutic targets in metastatic melanoma. RESULTS: The 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. CONCLUSION: Even 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. John Wiley and Sons Inc. 2023-05-11 /pmc/articles/PMC10358257/ /pubmed/37170733 http://dx.doi.org/10.1002/cam4.6055 Text en © 2023 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle REVIEWS
Basson, Charlise
Serem, June Cheptoo
Bipath, Priyesh
Hlophe, Yvette Nkondo
Chemokines as possible therapeutic targets in metastatic melanoma
title Chemokines as possible therapeutic targets in metastatic melanoma
title_full Chemokines as possible therapeutic targets in metastatic melanoma
title_fullStr Chemokines as possible therapeutic targets in metastatic melanoma
title_full_unstemmed Chemokines as possible therapeutic targets in metastatic melanoma
title_short Chemokines as possible therapeutic targets in metastatic melanoma
title_sort chemokines as possible therapeutic targets in metastatic melanoma
topic REVIEWS
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10358257/
https://www.ncbi.nlm.nih.gov/pubmed/37170733
http://dx.doi.org/10.1002/cam4.6055
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