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Cytokine secretion in breast cancer cells – MILLIPLEX assay data

Metastatic breast cancer is the most advanced stage of breast cancer and the leading cause of breast cancer mortality. Although understanding of the cancer progression and metastasis process has improved, the bi-directional communication between the tumor cell and the tumor microenvironment is still...

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Autores principales: Chen, Karin, Satlof, Leo, Stoffels, Guillaume, Kothapalli, Udithi, Ziluck, Noah, Lema, Maribel, Poretsky, Leonid, Avtanski, Dimiter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6889457/
https://www.ncbi.nlm.nih.gov/pubmed/31828190
http://dx.doi.org/10.1016/j.dib.2019.104798
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author Chen, Karin
Satlof, Leo
Stoffels, Guillaume
Kothapalli, Udithi
Ziluck, Noah
Lema, Maribel
Poretsky, Leonid
Avtanski, Dimiter
author_facet Chen, Karin
Satlof, Leo
Stoffels, Guillaume
Kothapalli, Udithi
Ziluck, Noah
Lema, Maribel
Poretsky, Leonid
Avtanski, Dimiter
author_sort Chen, Karin
collection PubMed
description Metastatic breast cancer is the most advanced stage of breast cancer and the leading cause of breast cancer mortality. Although understanding of the cancer progression and metastasis process has improved, the bi-directional communication between the tumor cell and the tumor microenvironment is still not well understood. Breast cancer cells are highly secretory, and their secretory activity is modulated by a variety of inflammatory stimuli present in the tumor microenvironment. Here, we characterized the cytokine expression in human breast cancer cells (MDA-MB-231, MCF-7, T-47D, and BT-474) in vitro using 41 cytokine MILLIPLEX assay. Further, we compared cytokine expression in breast cancer cells to those in non-tumorigenic human breast epithelial MCF-10A cells.
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spelling pubmed-68894572019-12-11 Cytokine secretion in breast cancer cells – MILLIPLEX assay data Chen, Karin Satlof, Leo Stoffels, Guillaume Kothapalli, Udithi Ziluck, Noah Lema, Maribel Poretsky, Leonid Avtanski, Dimiter Data Brief Biochemistry, Genetics and Molecular Biology Metastatic breast cancer is the most advanced stage of breast cancer and the leading cause of breast cancer mortality. Although understanding of the cancer progression and metastasis process has improved, the bi-directional communication between the tumor cell and the tumor microenvironment is still not well understood. Breast cancer cells are highly secretory, and their secretory activity is modulated by a variety of inflammatory stimuli present in the tumor microenvironment. Here, we characterized the cytokine expression in human breast cancer cells (MDA-MB-231, MCF-7, T-47D, and BT-474) in vitro using 41 cytokine MILLIPLEX assay. Further, we compared cytokine expression in breast cancer cells to those in non-tumorigenic human breast epithelial MCF-10A cells. Elsevier 2019-11-14 /pmc/articles/PMC6889457/ /pubmed/31828190 http://dx.doi.org/10.1016/j.dib.2019.104798 Text en © 2019 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Biochemistry, Genetics and Molecular Biology
Chen, Karin
Satlof, Leo
Stoffels, Guillaume
Kothapalli, Udithi
Ziluck, Noah
Lema, Maribel
Poretsky, Leonid
Avtanski, Dimiter
Cytokine secretion in breast cancer cells – MILLIPLEX assay data
title Cytokine secretion in breast cancer cells – MILLIPLEX assay data
title_full Cytokine secretion in breast cancer cells – MILLIPLEX assay data
title_fullStr Cytokine secretion in breast cancer cells – MILLIPLEX assay data
title_full_unstemmed Cytokine secretion in breast cancer cells – MILLIPLEX assay data
title_short Cytokine secretion in breast cancer cells – MILLIPLEX assay data
title_sort cytokine secretion in breast cancer cells – milliplex assay data
topic Biochemistry, Genetics and Molecular Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6889457/
https://www.ncbi.nlm.nih.gov/pubmed/31828190
http://dx.doi.org/10.1016/j.dib.2019.104798
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