Chemokine Pathways in Cutaneous Melanoma: Their Modulation by Cancer and Exploitation by the Clinician
The incidence of cutaneous malignant melanoma is rising globally and is projected to continue to rise. Advances in immunotherapy over the last decade have demonstrated that manipulation of the immune cell compartment of tumours is a valuable weapon in the arsenal against cancer; however, limitations...
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MDPI AG
2021
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oai:doaj.org-article:cb8c784ab84545ffbb1f0652f52eebaa2021-11-25T17:01:45ZChemokine Pathways in Cutaneous Melanoma: Their Modulation by Cancer and Exploitation by the Clinician10.3390/cancers132256252072-6694https://doaj.org/article/cb8c784ab84545ffbb1f0652f52eebaa2021-11-01T00:00:00Zhttps://www.mdpi.com/2072-6694/13/22/5625https://doaj.org/toc/2072-6694The incidence of cutaneous malignant melanoma is rising globally and is projected to continue to rise. Advances in immunotherapy over the last decade have demonstrated that manipulation of the immune cell compartment of tumours is a valuable weapon in the arsenal against cancer; however, limitations to treatment still exist. Cutaneous melanoma lesions feature a dense cell infiltrate, coordinated by chemokines, which control the positioning of all immune cells. Melanomas are able to use chemokine pathways to preferentially recruit cells, which aid their growth, survival, invasion and metastasis, and which enhance their ability to evade anticancer immune responses. Aside from this, chemokine signalling can directly influence angiogenesis, invasion, lymph node, and distal metastases, including epithelial to mesenchymal transition-like processes and transendothelial migration. Understanding the interplay of chemokines, cancer cells, and immune cells may uncover future avenues for melanoma therapy, namely: identifying biomarkers for patient stratification, augmenting the effect of current and emerging therapies, and designing specific treatments to target chemokine pathways, with the aim to reduce melanoma pathogenicity, metastatic potential, and enhance immune cell-mediated cancer killing. The chemokine network may provide selective and specific targets that, if included in current therapeutic regimens, harbour potential to improve outcomes for patients.Rebecca AdamsBernhard MoserSophia N. KaragiannisKatie E. LacyMDPI AGarticlechemokinesmelanomatumour pathogenicityimmunotherapybiomarkerstargeted therapyNeoplasms. Tumors. Oncology. Including cancer and carcinogensRC254-282ENCancers, Vol 13, Iss 5625, p 5625 (2021) |
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chemokines melanoma tumour pathogenicity immunotherapy biomarkers targeted therapy Neoplasms. Tumors. Oncology. Including cancer and carcinogens RC254-282 |
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chemokines melanoma tumour pathogenicity immunotherapy biomarkers targeted therapy Neoplasms. Tumors. Oncology. Including cancer and carcinogens RC254-282 Rebecca Adams Bernhard Moser Sophia N. Karagiannis Katie E. Lacy Chemokine Pathways in Cutaneous Melanoma: Their Modulation by Cancer and Exploitation by the Clinician |
description |
The incidence of cutaneous malignant melanoma is rising globally and is projected to continue to rise. Advances in immunotherapy over the last decade have demonstrated that manipulation of the immune cell compartment of tumours is a valuable weapon in the arsenal against cancer; however, limitations to treatment still exist. Cutaneous melanoma lesions feature a dense cell infiltrate, coordinated by chemokines, which control the positioning of all immune cells. Melanomas are able to use chemokine pathways to preferentially recruit cells, which aid their growth, survival, invasion and metastasis, and which enhance their ability to evade anticancer immune responses. Aside from this, chemokine signalling can directly influence angiogenesis, invasion, lymph node, and distal metastases, including epithelial to mesenchymal transition-like processes and transendothelial migration. Understanding the interplay of chemokines, cancer cells, and immune cells may uncover future avenues for melanoma therapy, namely: identifying biomarkers for patient stratification, augmenting the effect of current and emerging therapies, and designing specific treatments to target chemokine pathways, with the aim to reduce melanoma pathogenicity, metastatic potential, and enhance immune cell-mediated cancer killing. The chemokine network may provide selective and specific targets that, if included in current therapeutic regimens, harbour potential to improve outcomes for patients. |
format |
article |
author |
Rebecca Adams Bernhard Moser Sophia N. Karagiannis Katie E. Lacy |
author_facet |
Rebecca Adams Bernhard Moser Sophia N. Karagiannis Katie E. Lacy |
author_sort |
Rebecca Adams |
title |
Chemokine Pathways in Cutaneous Melanoma: Their Modulation by Cancer and Exploitation by the Clinician |
title_short |
Chemokine Pathways in Cutaneous Melanoma: Their Modulation by Cancer and Exploitation by the Clinician |
title_full |
Chemokine Pathways in Cutaneous Melanoma: Their Modulation by Cancer and Exploitation by the Clinician |
title_fullStr |
Chemokine Pathways in Cutaneous Melanoma: Their Modulation by Cancer and Exploitation by the Clinician |
title_full_unstemmed |
Chemokine Pathways in Cutaneous Melanoma: Their Modulation by Cancer and Exploitation by the Clinician |
title_sort |
chemokine pathways in cutaneous melanoma: their modulation by cancer and exploitation by the clinician |
publisher |
MDPI AG |
publishDate |
2021 |
url |
https://doaj.org/article/cb8c784ab84545ffbb1f0652f52eebaa |
work_keys_str_mv |
AT rebeccaadams chemokinepathwaysincutaneousmelanomatheirmodulationbycancerandexploitationbytheclinician AT bernhardmoser chemokinepathwaysincutaneousmelanomatheirmodulationbycancerandexploitationbytheclinician AT sophiankaragiannis chemokinepathwaysincutaneousmelanomatheirmodulationbycancerandexploitationbytheclinician AT katieelacy chemokinepathwaysincutaneousmelanomatheirmodulationbycancerandexploitationbytheclinician |
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