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Inhibition of dendritic cell differentiation and accumulation of myeloid-derived suppressor cells in cancer is regulated by S100A9 protein
Accumulation of myeloid-derived suppressor cells (MDSCs) associated with inhibition of dendritic cell (DC) differentiation is one of the major immunological abnormalities in cancer and leads to suppression of antitumor immune responses. The molecular mechanism of this phenomenon remains unclear. We...
Autores principales: | , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2556797/ https://www.ncbi.nlm.nih.gov/pubmed/18809714 http://dx.doi.org/10.1084/jem.20080132 |
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author | Cheng, Pingyan Corzo, Cesar A. Luetteke, Noreen Yu, Bin Nagaraj, Srinivas Bui, Marylin M. Ortiz, Myrna Nacken, Wolfgang Sorg, Clemens Vogl, Thomas Roth, Johannes Gabrilovich, Dmitry I. |
author_facet | Cheng, Pingyan Corzo, Cesar A. Luetteke, Noreen Yu, Bin Nagaraj, Srinivas Bui, Marylin M. Ortiz, Myrna Nacken, Wolfgang Sorg, Clemens Vogl, Thomas Roth, Johannes Gabrilovich, Dmitry I. |
author_sort | Cheng, Pingyan |
collection | PubMed |
description | Accumulation of myeloid-derived suppressor cells (MDSCs) associated with inhibition of dendritic cell (DC) differentiation is one of the major immunological abnormalities in cancer and leads to suppression of antitumor immune responses. The molecular mechanism of this phenomenon remains unclear. We report here that STAT3-inducible up-regulation of the myeloid-related protein S100A9 enhances MDSC production in cancer. Mice lacking this protein mounted potent antitumor immune responses and rejected implanted tumors. This effect was reversed by administration of wild-type MDSCs from tumor-bearing mice to S100A9-null mice. Overexpression of S100A9 in cultured embryonic stem cells or transgenic mice inhibited the differentiation of DCs and macrophages and induced accumulation of MDSCs. This study demonstrates that tumor-induced up-regulation of S100A9 protein is critically important for accumulation of MDSCs and reveals a novel molecular mechanism of immunological abnormalities in cancer. |
format | Text |
id | pubmed-2556797 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-25567972009-03-29 Inhibition of dendritic cell differentiation and accumulation of myeloid-derived suppressor cells in cancer is regulated by S100A9 protein Cheng, Pingyan Corzo, Cesar A. Luetteke, Noreen Yu, Bin Nagaraj, Srinivas Bui, Marylin M. Ortiz, Myrna Nacken, Wolfgang Sorg, Clemens Vogl, Thomas Roth, Johannes Gabrilovich, Dmitry I. J Exp Med Articles Accumulation of myeloid-derived suppressor cells (MDSCs) associated with inhibition of dendritic cell (DC) differentiation is one of the major immunological abnormalities in cancer and leads to suppression of antitumor immune responses. The molecular mechanism of this phenomenon remains unclear. We report here that STAT3-inducible up-regulation of the myeloid-related protein S100A9 enhances MDSC production in cancer. Mice lacking this protein mounted potent antitumor immune responses and rejected implanted tumors. This effect was reversed by administration of wild-type MDSCs from tumor-bearing mice to S100A9-null mice. Overexpression of S100A9 in cultured embryonic stem cells or transgenic mice inhibited the differentiation of DCs and macrophages and induced accumulation of MDSCs. This study demonstrates that tumor-induced up-regulation of S100A9 protein is critically important for accumulation of MDSCs and reveals a novel molecular mechanism of immunological abnormalities in cancer. The Rockefeller University Press 2008-09-29 /pmc/articles/PMC2556797/ /pubmed/18809714 http://dx.doi.org/10.1084/jem.20080132 Text en © 2008 Cheng et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.jem.org/misc/terms.shtml). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Articles Cheng, Pingyan Corzo, Cesar A. Luetteke, Noreen Yu, Bin Nagaraj, Srinivas Bui, Marylin M. Ortiz, Myrna Nacken, Wolfgang Sorg, Clemens Vogl, Thomas Roth, Johannes Gabrilovich, Dmitry I. Inhibition of dendritic cell differentiation and accumulation of myeloid-derived suppressor cells in cancer is regulated by S100A9 protein |
title | Inhibition of dendritic cell differentiation and accumulation of myeloid-derived suppressor cells in cancer is regulated by S100A9 protein |
title_full | Inhibition of dendritic cell differentiation and accumulation of myeloid-derived suppressor cells in cancer is regulated by S100A9 protein |
title_fullStr | Inhibition of dendritic cell differentiation and accumulation of myeloid-derived suppressor cells in cancer is regulated by S100A9 protein |
title_full_unstemmed | Inhibition of dendritic cell differentiation and accumulation of myeloid-derived suppressor cells in cancer is regulated by S100A9 protein |
title_short | Inhibition of dendritic cell differentiation and accumulation of myeloid-derived suppressor cells in cancer is regulated by S100A9 protein |
title_sort | inhibition of dendritic cell differentiation and accumulation of myeloid-derived suppressor cells in cancer is regulated by s100a9 protein |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2556797/ https://www.ncbi.nlm.nih.gov/pubmed/18809714 http://dx.doi.org/10.1084/jem.20080132 |
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