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Expression of Forkhead box P3 in tumour cells causes immunoregulatory function of signet ring cell carcinoma of the stomach
BACKGROUND: It was recently reported that the transcription factor Forkhead box P3 (FoxP3) is expressed not only in regulatory T cells (Tregs) but also in cancer cells. The aim of this study was to clarify the clinical significance of FoxP3 expression in gastric carcinoma. METHODS: We performed immu...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3349176/ https://www.ncbi.nlm.nih.gov/pubmed/22569001 http://dx.doi.org/10.1038/bjc.2012.141 |
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author | Yoshii, M Tanaka, H Ohira, M Muguruma, K Iwauchi, T Lee, T Sakurai, K Kubo, N Yashiro, M Sawada, T Hirakawa, K |
author_facet | Yoshii, M Tanaka, H Ohira, M Muguruma, K Iwauchi, T Lee, T Sakurai, K Kubo, N Yashiro, M Sawada, T Hirakawa, K |
author_sort | Yoshii, M |
collection | PubMed |
description | BACKGROUND: It was recently reported that the transcription factor Forkhead box P3 (FoxP3) is expressed not only in regulatory T cells (Tregs) but also in cancer cells. The aim of this study was to clarify the clinical significance of FoxP3 expression in gastric carcinoma. METHODS: We performed immunohistochemical staining of FoxP3 to examine the association of FoxP3 expression with clinicopathological features of 194 patients with gastric cancer who underwent surgical resection from 2000 to 2010. We also investigated the immunosuppressive function of FoxP3 using gastric cancer cell lines. RESULTS: Immunohistochemical staining indicated FoxP3-positive cells within tumour tissue including both Tregs and tumour cells. Forkhead box P3-positive tumour cells were observed in 79.3% of signet ring cell carcinoma patients, and the expression of FoxP3 showed a significant correlation with lymph node metastasis. We showed that transforming growth factor-β augmented FoxP3 mRNA expression in cell lines derived from signet ring cell carcinoma. Indoleamine-2,3-dioxygenase and galectin-1, key effectors of Treg-mediated immunosuppression, were downregulated by FoxP3 knockdown. CONCLUSION: Our findings suggested that FoxP3 expression by tumour cells might have important roles in immune escape of gastric carcinoma, and be associated with the malignant potential of scirrhous gastric carcinoma. |
format | Online Article Text |
id | pubmed-3349176 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-33491762013-05-08 Expression of Forkhead box P3 in tumour cells causes immunoregulatory function of signet ring cell carcinoma of the stomach Yoshii, M Tanaka, H Ohira, M Muguruma, K Iwauchi, T Lee, T Sakurai, K Kubo, N Yashiro, M Sawada, T Hirakawa, K Br J Cancer Molecular Diagnostics BACKGROUND: It was recently reported that the transcription factor Forkhead box P3 (FoxP3) is expressed not only in regulatory T cells (Tregs) but also in cancer cells. The aim of this study was to clarify the clinical significance of FoxP3 expression in gastric carcinoma. METHODS: We performed immunohistochemical staining of FoxP3 to examine the association of FoxP3 expression with clinicopathological features of 194 patients with gastric cancer who underwent surgical resection from 2000 to 2010. We also investigated the immunosuppressive function of FoxP3 using gastric cancer cell lines. RESULTS: Immunohistochemical staining indicated FoxP3-positive cells within tumour tissue including both Tregs and tumour cells. Forkhead box P3-positive tumour cells were observed in 79.3% of signet ring cell carcinoma patients, and the expression of FoxP3 showed a significant correlation with lymph node metastasis. We showed that transforming growth factor-β augmented FoxP3 mRNA expression in cell lines derived from signet ring cell carcinoma. Indoleamine-2,3-dioxygenase and galectin-1, key effectors of Treg-mediated immunosuppression, were downregulated by FoxP3 knockdown. CONCLUSION: Our findings suggested that FoxP3 expression by tumour cells might have important roles in immune escape of gastric carcinoma, and be associated with the malignant potential of scirrhous gastric carcinoma. Nature Publishing Group 2012-05-08 2012-04-19 /pmc/articles/PMC3349176/ /pubmed/22569001 http://dx.doi.org/10.1038/bjc.2012.141 Text en Copyright © 2012 Cancer Research UK https://creativecommons.org/licenses/by-nc-sa/3.0/From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/ |
spellingShingle | Molecular Diagnostics Yoshii, M Tanaka, H Ohira, M Muguruma, K Iwauchi, T Lee, T Sakurai, K Kubo, N Yashiro, M Sawada, T Hirakawa, K Expression of Forkhead box P3 in tumour cells causes immunoregulatory function of signet ring cell carcinoma of the stomach |
title | Expression of Forkhead box P3 in tumour cells causes immunoregulatory function
of signet ring cell carcinoma of the stomach |
title_full | Expression of Forkhead box P3 in tumour cells causes immunoregulatory function
of signet ring cell carcinoma of the stomach |
title_fullStr | Expression of Forkhead box P3 in tumour cells causes immunoregulatory function
of signet ring cell carcinoma of the stomach |
title_full_unstemmed | Expression of Forkhead box P3 in tumour cells causes immunoregulatory function
of signet ring cell carcinoma of the stomach |
title_short | Expression of Forkhead box P3 in tumour cells causes immunoregulatory function
of signet ring cell carcinoma of the stomach |
title_sort | expression of forkhead box p3 in tumour cells causes immunoregulatory function
of signet ring cell carcinoma of the stomach |
topic | Molecular Diagnostics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3349176/ https://www.ncbi.nlm.nih.gov/pubmed/22569001 http://dx.doi.org/10.1038/bjc.2012.141 |
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