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WSX1 Expression in Tumors Induces Immune Tolerance via Suppression of Effector Immune Cells
Crosstalk between tumor cells and the cognate microenvironment plays a crucial role in tumor initiation and progression. However, only a few genes are known to affect such a crosstalk. This study reveals that WSX1 plays such a role when highly expressed in tumor cells. The expression of WSX1 in Lewi...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3084744/ https://www.ncbi.nlm.nih.gov/pubmed/21559505 http://dx.doi.org/10.1371/journal.pone.0019072 |
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author | Dibra, Denada Cutrera, Jeffry Xia, Xueqing Li, Shulin |
author_facet | Dibra, Denada Cutrera, Jeffry Xia, Xueqing Li, Shulin |
author_sort | Dibra, Denada |
collection | PubMed |
description | Crosstalk between tumor cells and the cognate microenvironment plays a crucial role in tumor initiation and progression. However, only a few genes are known to affect such a crosstalk. This study reveals that WSX1 plays such a role when highly expressed in tumor cells. The expression of WSX1 in Lewis Lung Carcinoma (LLC) and the melanoma cell line AGS induces the death of T cells and inhibits the production of the effector cytokine IFNγ from NK and T cells, resulting in the promotion of tumor growth. These pro-tumorigenic properties of WSX1 are independent of IL27. This key observation reveals a new pathway of tumor-host interaction, which will ultimately lead to better strategies in immune therapy to reverse tumor tolerance. |
format | Text |
id | pubmed-3084744 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-30847442011-05-10 WSX1 Expression in Tumors Induces Immune Tolerance via Suppression of Effector Immune Cells Dibra, Denada Cutrera, Jeffry Xia, Xueqing Li, Shulin PLoS One Research Article Crosstalk between tumor cells and the cognate microenvironment plays a crucial role in tumor initiation and progression. However, only a few genes are known to affect such a crosstalk. This study reveals that WSX1 plays such a role when highly expressed in tumor cells. The expression of WSX1 in Lewis Lung Carcinoma (LLC) and the melanoma cell line AGS induces the death of T cells and inhibits the production of the effector cytokine IFNγ from NK and T cells, resulting in the promotion of tumor growth. These pro-tumorigenic properties of WSX1 are independent of IL27. This key observation reveals a new pathway of tumor-host interaction, which will ultimately lead to better strategies in immune therapy to reverse tumor tolerance. Public Library of Science 2011-04-29 /pmc/articles/PMC3084744/ /pubmed/21559505 http://dx.doi.org/10.1371/journal.pone.0019072 Text en Dibra 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 Dibra, Denada Cutrera, Jeffry Xia, Xueqing Li, Shulin WSX1 Expression in Tumors Induces Immune Tolerance via Suppression of Effector Immune Cells |
title | WSX1 Expression in Tumors Induces Immune Tolerance via Suppression of Effector Immune Cells |
title_full | WSX1 Expression in Tumors Induces Immune Tolerance via Suppression of Effector Immune Cells |
title_fullStr | WSX1 Expression in Tumors Induces Immune Tolerance via Suppression of Effector Immune Cells |
title_full_unstemmed | WSX1 Expression in Tumors Induces Immune Tolerance via Suppression of Effector Immune Cells |
title_short | WSX1 Expression in Tumors Induces Immune Tolerance via Suppression of Effector Immune Cells |
title_sort | wsx1 expression in tumors induces immune tolerance via suppression of effector immune cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3084744/ https://www.ncbi.nlm.nih.gov/pubmed/21559505 http://dx.doi.org/10.1371/journal.pone.0019072 |
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