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Human breast cancer-derived soluble factors facilitate CCL19-induced chemotaxis of human dendritic cells

Breast cancer remains as a challenging disease with high mortality in women. Increasing evidence points the importance of understanding a crosstalk between breast cancers and immune cells, but little is known about the effect of breast cancer-derived factors on the migratory properties of dendritic...

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Autores principales: Hwang, Hyundoo, Shin, Changsik, Park, Juhee, Kang, Enoch, Choi, Bongseo, Han, Jae-A, Do, Yoonkyung, Ryu, Seongho, Cho, Yoon-Kyoung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4958978/
https://www.ncbi.nlm.nih.gov/pubmed/27451948
http://dx.doi.org/10.1038/srep30207
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author Hwang, Hyundoo
Shin, Changsik
Park, Juhee
Kang, Enoch
Choi, Bongseo
Han, Jae-A
Do, Yoonkyung
Ryu, Seongho
Cho, Yoon-Kyoung
author_facet Hwang, Hyundoo
Shin, Changsik
Park, Juhee
Kang, Enoch
Choi, Bongseo
Han, Jae-A
Do, Yoonkyung
Ryu, Seongho
Cho, Yoon-Kyoung
author_sort Hwang, Hyundoo
collection PubMed
description Breast cancer remains as a challenging disease with high mortality in women. Increasing evidence points the importance of understanding a crosstalk between breast cancers and immune cells, but little is known about the effect of breast cancer-derived factors on the migratory properties of dendritic cells (DCs) and their consequent capability in inducing T cell immune responses. Utilizing a unique 3D microfluidic device, we here showed that breast cancers (MCF-7, MDA-MB-231, MDA-MB-436 and SK-BR-3)-derived soluble factors increase the migration of DCs toward CCL19. The enhanced migration of DCs was mainly mediated via the highly activated JNK/c-Jun signaling pathway, increasing their directional persistence, while the velocity of DCs was not influenced, particularly when they were co-cultured with triple negative breast cancer cells (TNBCs or MDA-MB-231 and MDA-MB-436). The DCs up-regulated inflammatory cytokines IL-1β and IL-6 and induced T cells more proliferative and resistant against activation-induced cell death (AICD), which secret high levels of inflammatory cytokines IL-1β, IL-6 and IFN-γ. This study demonstrated new possible evasion strategy of TNBCs utilizing their soluble factors that exploit the directionality of DCs toward chemokine responses, leading to the building of inflammatory milieu which may support their own growth.
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spelling pubmed-49589782016-08-04 Human breast cancer-derived soluble factors facilitate CCL19-induced chemotaxis of human dendritic cells Hwang, Hyundoo Shin, Changsik Park, Juhee Kang, Enoch Choi, Bongseo Han, Jae-A Do, Yoonkyung Ryu, Seongho Cho, Yoon-Kyoung Sci Rep Article Breast cancer remains as a challenging disease with high mortality in women. Increasing evidence points the importance of understanding a crosstalk between breast cancers and immune cells, but little is known about the effect of breast cancer-derived factors on the migratory properties of dendritic cells (DCs) and their consequent capability in inducing T cell immune responses. Utilizing a unique 3D microfluidic device, we here showed that breast cancers (MCF-7, MDA-MB-231, MDA-MB-436 and SK-BR-3)-derived soluble factors increase the migration of DCs toward CCL19. The enhanced migration of DCs was mainly mediated via the highly activated JNK/c-Jun signaling pathway, increasing their directional persistence, while the velocity of DCs was not influenced, particularly when they were co-cultured with triple negative breast cancer cells (TNBCs or MDA-MB-231 and MDA-MB-436). The DCs up-regulated inflammatory cytokines IL-1β and IL-6 and induced T cells more proliferative and resistant against activation-induced cell death (AICD), which secret high levels of inflammatory cytokines IL-1β, IL-6 and IFN-γ. This study demonstrated new possible evasion strategy of TNBCs utilizing their soluble factors that exploit the directionality of DCs toward chemokine responses, leading to the building of inflammatory milieu which may support their own growth. Nature Publishing Group 2016-07-25 /pmc/articles/PMC4958978/ /pubmed/27451948 http://dx.doi.org/10.1038/srep30207 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Hwang, Hyundoo
Shin, Changsik
Park, Juhee
Kang, Enoch
Choi, Bongseo
Han, Jae-A
Do, Yoonkyung
Ryu, Seongho
Cho, Yoon-Kyoung
Human breast cancer-derived soluble factors facilitate CCL19-induced chemotaxis of human dendritic cells
title Human breast cancer-derived soluble factors facilitate CCL19-induced chemotaxis of human dendritic cells
title_full Human breast cancer-derived soluble factors facilitate CCL19-induced chemotaxis of human dendritic cells
title_fullStr Human breast cancer-derived soluble factors facilitate CCL19-induced chemotaxis of human dendritic cells
title_full_unstemmed Human breast cancer-derived soluble factors facilitate CCL19-induced chemotaxis of human dendritic cells
title_short Human breast cancer-derived soluble factors facilitate CCL19-induced chemotaxis of human dendritic cells
title_sort human breast cancer-derived soluble factors facilitate ccl19-induced chemotaxis of human dendritic cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4958978/
https://www.ncbi.nlm.nih.gov/pubmed/27451948
http://dx.doi.org/10.1038/srep30207
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