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Stromal Cells Positively and Negatively Modulate the Growth of Cancer Cells: Stimulation via the PGE2-TNFα-IL-6 Pathway and Inhibition via Secreted GAPDH-E-Cadherin Interaction
Fibroblast-like stromal cells modulate cancer cells through secreted factors and adhesion, but those factors are not fully understood. Here, we have identified critical stromal factors that modulate cancer growth positively and negatively. Using a cell co-culture system, we found that gastric stroma...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4364666/ https://www.ncbi.nlm.nih.gov/pubmed/25785838 http://dx.doi.org/10.1371/journal.pone.0119415 |
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author | Kawada, Manabu Inoue, Hiroyuki Ohba, Shun-ichi Yoshida, Junjiro Masuda, Tohru Yamasaki, Manabu Usami, Ihomi Sakamoto, Shuichi Abe, Hikaru Watanabe, Takumi Yamori, Takao Shibasaki, Masakatsu Nomoto, Akio |
author_facet | Kawada, Manabu Inoue, Hiroyuki Ohba, Shun-ichi Yoshida, Junjiro Masuda, Tohru Yamasaki, Manabu Usami, Ihomi Sakamoto, Shuichi Abe, Hikaru Watanabe, Takumi Yamori, Takao Shibasaki, Masakatsu Nomoto, Akio |
author_sort | Kawada, Manabu |
collection | PubMed |
description | Fibroblast-like stromal cells modulate cancer cells through secreted factors and adhesion, but those factors are not fully understood. Here, we have identified critical stromal factors that modulate cancer growth positively and negatively. Using a cell co-culture system, we found that gastric stromal cells secreted IL-6 as a growth and survival factor for gastric cancer cells. Moreover, gastric cancer cells secreted PGE2 and TNFα that stimulated IL-6 secretion by the stromal cells. Furthermore, we found that stromal cells secreted glyceraldehyde 3-phosphate dehydrogenase (GAPDH). Extracellular GAPDH, or its N-terminal domain, inhibited gastric cancer cell growth, a finding confirmed in other cell systems. GAPDH bound to E-cadherin and downregulated the mTOR-p70S6 kinase pathway. These results demonstrate that stromal cells could regulate cancer cell growth through the balance of these secreted factors. We propose that negative regulation of cancer growth using GAPDH could be a new anti-cancer strategy. |
format | Online Article Text |
id | pubmed-4364666 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-43646662015-03-23 Stromal Cells Positively and Negatively Modulate the Growth of Cancer Cells: Stimulation via the PGE2-TNFα-IL-6 Pathway and Inhibition via Secreted GAPDH-E-Cadherin Interaction Kawada, Manabu Inoue, Hiroyuki Ohba, Shun-ichi Yoshida, Junjiro Masuda, Tohru Yamasaki, Manabu Usami, Ihomi Sakamoto, Shuichi Abe, Hikaru Watanabe, Takumi Yamori, Takao Shibasaki, Masakatsu Nomoto, Akio PLoS One Research Article Fibroblast-like stromal cells modulate cancer cells through secreted factors and adhesion, but those factors are not fully understood. Here, we have identified critical stromal factors that modulate cancer growth positively and negatively. Using a cell co-culture system, we found that gastric stromal cells secreted IL-6 as a growth and survival factor for gastric cancer cells. Moreover, gastric cancer cells secreted PGE2 and TNFα that stimulated IL-6 secretion by the stromal cells. Furthermore, we found that stromal cells secreted glyceraldehyde 3-phosphate dehydrogenase (GAPDH). Extracellular GAPDH, or its N-terminal domain, inhibited gastric cancer cell growth, a finding confirmed in other cell systems. GAPDH bound to E-cadherin and downregulated the mTOR-p70S6 kinase pathway. These results demonstrate that stromal cells could regulate cancer cell growth through the balance of these secreted factors. We propose that negative regulation of cancer growth using GAPDH could be a new anti-cancer strategy. Public Library of Science 2015-03-18 /pmc/articles/PMC4364666/ /pubmed/25785838 http://dx.doi.org/10.1371/journal.pone.0119415 Text en © 2015 Kawada et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Kawada, Manabu Inoue, Hiroyuki Ohba, Shun-ichi Yoshida, Junjiro Masuda, Tohru Yamasaki, Manabu Usami, Ihomi Sakamoto, Shuichi Abe, Hikaru Watanabe, Takumi Yamori, Takao Shibasaki, Masakatsu Nomoto, Akio Stromal Cells Positively and Negatively Modulate the Growth of Cancer Cells: Stimulation via the PGE2-TNFα-IL-6 Pathway and Inhibition via Secreted GAPDH-E-Cadherin Interaction |
title | Stromal Cells Positively and Negatively Modulate the Growth of Cancer Cells: Stimulation via the PGE2-TNFα-IL-6 Pathway and Inhibition via Secreted GAPDH-E-Cadherin Interaction |
title_full | Stromal Cells Positively and Negatively Modulate the Growth of Cancer Cells: Stimulation via the PGE2-TNFα-IL-6 Pathway and Inhibition via Secreted GAPDH-E-Cadherin Interaction |
title_fullStr | Stromal Cells Positively and Negatively Modulate the Growth of Cancer Cells: Stimulation via the PGE2-TNFα-IL-6 Pathway and Inhibition via Secreted GAPDH-E-Cadherin Interaction |
title_full_unstemmed | Stromal Cells Positively and Negatively Modulate the Growth of Cancer Cells: Stimulation via the PGE2-TNFα-IL-6 Pathway and Inhibition via Secreted GAPDH-E-Cadherin Interaction |
title_short | Stromal Cells Positively and Negatively Modulate the Growth of Cancer Cells: Stimulation via the PGE2-TNFα-IL-6 Pathway and Inhibition via Secreted GAPDH-E-Cadherin Interaction |
title_sort | stromal cells positively and negatively modulate the growth of cancer cells: stimulation via the pge2-tnfα-il-6 pathway and inhibition via secreted gapdh-e-cadherin interaction |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4364666/ https://www.ncbi.nlm.nih.gov/pubmed/25785838 http://dx.doi.org/10.1371/journal.pone.0119415 |
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