CCR7 as a therapeutic target in Cancer.


Journal

Biochimica et biophysica acta. Reviews on cancer
ISSN: 1879-2561
Titre abrégé: Biochim Biophys Acta Rev Cancer
Pays: Netherlands
ID NLM: 9806362

Informations de publication

Date de publication:
01 2021
Historique:
received: 05 10 2020
revised: 24 12 2020
accepted: 24 12 2020
pubmed: 2 1 2021
medline: 15 4 2021
entrez: 1 1 2021
Statut: ppublish

Résumé

The CCR7 chemokine axis is comprised of chemokine ligand 21 (CCL21) and chemokine ligand 19 (CCL19) acting on chemokine receptor 7 (CCR7). This axis plays two important but apparently opposing roles in cancer. On the one hand, this axis is significantly engaged in the trafficking of a number of effecter cells involved in mounting an immune response to a growing tumour. This suggests therapeutic strategies which involve potentiation of this axis can be used to combat the spread of cancer. On the other hand, the CCR7 axis plays a significant role in controlling the migration of tumour cells towards the lymphatic system and metastasis and can thus contribute to the expansion of cancer. This implies that therapeutic strategies which involve decreasing signaling through the CCR7 axis would have a beneficial effect in preventing dissemination of cancer. This dichotomy has partly been the reason why this axis has not yet been exploited, as other chemokine axes have, as a therapeutic target in cancer. Recent report of a crystal structure for CCR7 provides opportunities to exploit this axis in developing new cancer therapies. However, it remains unclear which of these two strategies, potentiation or antagonism of the CCR7 axis, is more appropriate for cancer therapy. This review brings together the evidence supporting both roles of the CCR7 axis in cancer and examines the future potential of each of the two different therapeutic approaches involving the CCR7 axis in cancer.

Identifiants

pubmed: 33385485
pii: S0304-419X(20)30218-3
doi: 10.1016/j.bbcan.2020.188499
pii:
doi:

Substances chimiques

Biomarkers, Tumor 0
CCR7 protein, human 0
Ligands 0
Receptors, CCR7 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

188499

Informations de copyright

Copyright © 2020. Published by Elsevier B.V.

Auteurs

Anwar Salem (A)

Institute of Cancer Therapeutics, University of Bradford; Bradford BD7 1DP, United Kingdom.

Mashael Alotaibi (M)

Institute of Cancer Therapeutics, University of Bradford; Bradford BD7 1DP, United Kingdom.

Rima Mroueh (R)

Institute of Cancer Therapeutics, University of Bradford; Bradford BD7 1DP, United Kingdom.

Haneen A Basheer (HA)

Faculty of Pharmacy, Zarqa University, PO Box 132222, Zarqa 13132, Jordan.

Kamyar Afarinkia (K)

Institute of Cancer Therapeutics, University of Bradford; Bradford BD7 1DP, United Kingdom. Electronic address: k.afarinkia@bradford.ac.uk.

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Classifications MeSH