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A CCL8 gradient drives breast cancer cell dissemination

The migration of cancer cells towards gradients of chemoattractive factors represents a potential, yet elusive, mechanism that may contribute to cancer cell dissemination. Here we provide evidence for the maintenance of a gradient of increasing CCL8 concentration between the epithelium, the stroma a...

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Autores principales: Farmaki, Elena, Chatzistamou, Ioulia, Kaza, Vimala, Kiaris, Hippokratis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5112152/
https://www.ncbi.nlm.nih.gov/pubmed/27181207
http://dx.doi.org/10.1038/onc.2016.161
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author Farmaki, Elena
Chatzistamou, Ioulia
Kaza, Vimala
Kiaris, Hippokratis
author_facet Farmaki, Elena
Chatzistamou, Ioulia
Kaza, Vimala
Kiaris, Hippokratis
author_sort Farmaki, Elena
collection PubMed
description The migration of cancer cells towards gradients of chemoattractive factors represents a potential, yet elusive, mechanism that may contribute to cancer cell dissemination. Here we provide evidence for the maintenance of a gradient of increasing CCL8 concentration between the epithelium, the stroma and the periphery that is instrumental for breast cancer cells’ dissemination. In response to signals elicited by the neoplastic epithelium CCL8 production is enhanced in stromal fibroblasts at the tumor margins and in tissues at which breast cancer cells tend to metastasize such as the lungs and the brain. Manipulation of CCL8 activity influences the histology of the tumors and promotes major steps of the metastatic process such as invasion to adjacent stroma, intravasation and ultimately extravasation and seeding. These findings exemplify how gradients of chemoattractive factors such as CCL8, drive metastasis and suggest that interference with their operation may provide means for breast cancer management.
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spelling pubmed-51121522016-12-11 A CCL8 gradient drives breast cancer cell dissemination Farmaki, Elena Chatzistamou, Ioulia Kaza, Vimala Kiaris, Hippokratis Oncogene Article The migration of cancer cells towards gradients of chemoattractive factors represents a potential, yet elusive, mechanism that may contribute to cancer cell dissemination. Here we provide evidence for the maintenance of a gradient of increasing CCL8 concentration between the epithelium, the stroma and the periphery that is instrumental for breast cancer cells’ dissemination. In response to signals elicited by the neoplastic epithelium CCL8 production is enhanced in stromal fibroblasts at the tumor margins and in tissues at which breast cancer cells tend to metastasize such as the lungs and the brain. Manipulation of CCL8 activity influences the histology of the tumors and promotes major steps of the metastatic process such as invasion to adjacent stroma, intravasation and ultimately extravasation and seeding. These findings exemplify how gradients of chemoattractive factors such as CCL8, drive metastasis and suggest that interference with their operation may provide means for breast cancer management. 2016-05-16 2016-12-08 /pmc/articles/PMC5112152/ /pubmed/27181207 http://dx.doi.org/10.1038/onc.2016.161 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Farmaki, Elena
Chatzistamou, Ioulia
Kaza, Vimala
Kiaris, Hippokratis
A CCL8 gradient drives breast cancer cell dissemination
title A CCL8 gradient drives breast cancer cell dissemination
title_full A CCL8 gradient drives breast cancer cell dissemination
title_fullStr A CCL8 gradient drives breast cancer cell dissemination
title_full_unstemmed A CCL8 gradient drives breast cancer cell dissemination
title_short A CCL8 gradient drives breast cancer cell dissemination
title_sort ccl8 gradient drives breast cancer cell dissemination
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5112152/
https://www.ncbi.nlm.nih.gov/pubmed/27181207
http://dx.doi.org/10.1038/onc.2016.161
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