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The CXCL8-CXCR1/2 pathways in cancer

Persistent infection or chronic inflammation contributes significantly to tumourigenesis and tumour progression. C-X-C motif ligand 8 (CXCL8) is a chemokine that acts as an important multifunctional cytokine to modulate tumour proliferation, invasion and migration in an autocrine or paracrine manner...

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Detalles Bibliográficos
Autores principales: Liu, Qian, Li, Anping, Tian, Yijun, Wu, Jennifer D., Liu, Yu, Li, Tengfei, Chen, Yuan, Han, Xinwei, Wu, Kongming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6142815/
https://www.ncbi.nlm.nih.gov/pubmed/27578214
http://dx.doi.org/10.1016/j.cytogfr.2016.08.002
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author Liu, Qian
Li, Anping
Tian, Yijun
Wu, Jennifer D.
Liu, Yu
Li, Tengfei
Chen, Yuan
Han, Xinwei
Wu, Kongming
author_facet Liu, Qian
Li, Anping
Tian, Yijun
Wu, Jennifer D.
Liu, Yu
Li, Tengfei
Chen, Yuan
Han, Xinwei
Wu, Kongming
author_sort Liu, Qian
collection PubMed
description Persistent infection or chronic inflammation contributes significantly to tumourigenesis and tumour progression. C-X-C motif ligand 8 (CXCL8) is a chemokine that acts as an important multifunctional cytokine to modulate tumour proliferation, invasion and migration in an autocrine or paracrine manner. Studies have suggested that CXCL8 and its cognate receptors, C-X-C chemokine receptor 1 (CXCR1) and CX-C chemokine receptor 2 (CXCR2), mediate the initiation and development of various cancers including breast cancer, prostate cancer, lung cancer, colorectal carcinoma and melanoma. CXCL8 also integrates with multiple intracellular signalling pathways to produce coordinated effects. Neovascularisation, which provides a basis for fostering tumour growth and metastasis, is now recognised as a critical function of CXCL8 in the tumour microenvironment. In this review, we summarize the biological functions and ficlinical significance of the CXCL8 signalling axis in cancer. We also propose that CXCL8 may be a potential therapeutic target for cancer treatment
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spelling pubmed-61428152018-09-18 The CXCL8-CXCR1/2 pathways in cancer Liu, Qian Li, Anping Tian, Yijun Wu, Jennifer D. Liu, Yu Li, Tengfei Chen, Yuan Han, Xinwei Wu, Kongming Cytokine Growth Factor Rev Article Persistent infection or chronic inflammation contributes significantly to tumourigenesis and tumour progression. C-X-C motif ligand 8 (CXCL8) is a chemokine that acts as an important multifunctional cytokine to modulate tumour proliferation, invasion and migration in an autocrine or paracrine manner. Studies have suggested that CXCL8 and its cognate receptors, C-X-C chemokine receptor 1 (CXCR1) and CX-C chemokine receptor 2 (CXCR2), mediate the initiation and development of various cancers including breast cancer, prostate cancer, lung cancer, colorectal carcinoma and melanoma. CXCL8 also integrates with multiple intracellular signalling pathways to produce coordinated effects. Neovascularisation, which provides a basis for fostering tumour growth and metastasis, is now recognised as a critical function of CXCL8 in the tumour microenvironment. In this review, we summarize the biological functions and ficlinical significance of the CXCL8 signalling axis in cancer. We also propose that CXCL8 may be a potential therapeutic target for cancer treatment 2016-08-25 2016-10 /pmc/articles/PMC6142815/ /pubmed/27578214 http://dx.doi.org/10.1016/j.cytogfr.2016.08.002 Text en This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Liu, Qian
Li, Anping
Tian, Yijun
Wu, Jennifer D.
Liu, Yu
Li, Tengfei
Chen, Yuan
Han, Xinwei
Wu, Kongming
The CXCL8-CXCR1/2 pathways in cancer
title The CXCL8-CXCR1/2 pathways in cancer
title_full The CXCL8-CXCR1/2 pathways in cancer
title_fullStr The CXCL8-CXCR1/2 pathways in cancer
title_full_unstemmed The CXCL8-CXCR1/2 pathways in cancer
title_short The CXCL8-CXCR1/2 pathways in cancer
title_sort cxcl8-cxcr1/2 pathways in cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6142815/
https://www.ncbi.nlm.nih.gov/pubmed/27578214
http://dx.doi.org/10.1016/j.cytogfr.2016.08.002
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