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Foxp3 expression in human cancer cells
OBJECTIVE: Transcription factor forkhead box protein 3 (Foxp3) specifically characterizes the thymically derived naturally occurring regulatory T cells (Tregs). Limited evidence indicates that it is also expressed, albeit to a lesser extent, in tissues other than thymus and spleen, while, very recen...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2386447/ https://www.ncbi.nlm.nih.gov/pubmed/18430198 http://dx.doi.org/10.1186/1479-5876-6-19 |
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author | Karanikas, Vaios Speletas, Matthaios Zamanakou, Maria Kalala, Fani Loules, Gedeon Kerenidi, Theodora Barda, Angeliki K Gourgoulianis, Konstantinos I Germenis, Anastasios E |
author_facet | Karanikas, Vaios Speletas, Matthaios Zamanakou, Maria Kalala, Fani Loules, Gedeon Kerenidi, Theodora Barda, Angeliki K Gourgoulianis, Konstantinos I Germenis, Anastasios E |
author_sort | Karanikas, Vaios |
collection | PubMed |
description | OBJECTIVE: Transcription factor forkhead box protein 3 (Foxp3) specifically characterizes the thymically derived naturally occurring regulatory T cells (Tregs). Limited evidence indicates that it is also expressed, albeit to a lesser extent, in tissues other than thymus and spleen, while, very recently, it was shown that Foxp3 is expressed by pancreatic carcinoma. This study was scheduled to investigate whether expression of Foxp3 transcripts and mature protein occurs constitutively in various tumor types. MATERIALS AND METHODS: Twenty five tumor cell lines of different tissue origins (lung cancer, colon cancer, breast cancer, melanoma, erythroid leukemia, acute T-cell leukemia) were studied. Detection of Foxp3 mRNA was performed using both conventional RT-PCR and quantitative real-time PCR while protein expression was assessed by immunocytochemistry and flow cytometry, using different antibody clones. RESULTS: Foxp3 mRNA as well as Foxp3 protein was detected in all tumor cell lines, albeit in variable levels, not related to the tissue of origin. This expression correlated with the expression levels of IL-10 and TGFb1. CONCLUSION: We offer evidence that Foxp3 expression, characterizes tumor cells of various tissue origins. The biological significance of these findings warrants further investigation in the context of tumor immune escape, and especially under the light of current anti-cancer efforts interfering with Foxp3 expression. |
format | Text |
id | pubmed-2386447 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-23864472008-05-16 Foxp3 expression in human cancer cells Karanikas, Vaios Speletas, Matthaios Zamanakou, Maria Kalala, Fani Loules, Gedeon Kerenidi, Theodora Barda, Angeliki K Gourgoulianis, Konstantinos I Germenis, Anastasios E J Transl Med Research OBJECTIVE: Transcription factor forkhead box protein 3 (Foxp3) specifically characterizes the thymically derived naturally occurring regulatory T cells (Tregs). Limited evidence indicates that it is also expressed, albeit to a lesser extent, in tissues other than thymus and spleen, while, very recently, it was shown that Foxp3 is expressed by pancreatic carcinoma. This study was scheduled to investigate whether expression of Foxp3 transcripts and mature protein occurs constitutively in various tumor types. MATERIALS AND METHODS: Twenty five tumor cell lines of different tissue origins (lung cancer, colon cancer, breast cancer, melanoma, erythroid leukemia, acute T-cell leukemia) were studied. Detection of Foxp3 mRNA was performed using both conventional RT-PCR and quantitative real-time PCR while protein expression was assessed by immunocytochemistry and flow cytometry, using different antibody clones. RESULTS: Foxp3 mRNA as well as Foxp3 protein was detected in all tumor cell lines, albeit in variable levels, not related to the tissue of origin. This expression correlated with the expression levels of IL-10 and TGFb1. CONCLUSION: We offer evidence that Foxp3 expression, characterizes tumor cells of various tissue origins. The biological significance of these findings warrants further investigation in the context of tumor immune escape, and especially under the light of current anti-cancer efforts interfering with Foxp3 expression. BioMed Central 2008-04-22 /pmc/articles/PMC2386447/ /pubmed/18430198 http://dx.doi.org/10.1186/1479-5876-6-19 Text en Copyright © 2008 Karanikas et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Karanikas, Vaios Speletas, Matthaios Zamanakou, Maria Kalala, Fani Loules, Gedeon Kerenidi, Theodora Barda, Angeliki K Gourgoulianis, Konstantinos I Germenis, Anastasios E Foxp3 expression in human cancer cells |
title | Foxp3 expression in human cancer cells |
title_full | Foxp3 expression in human cancer cells |
title_fullStr | Foxp3 expression in human cancer cells |
title_full_unstemmed | Foxp3 expression in human cancer cells |
title_short | Foxp3 expression in human cancer cells |
title_sort | foxp3 expression in human cancer cells |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2386447/ https://www.ncbi.nlm.nih.gov/pubmed/18430198 http://dx.doi.org/10.1186/1479-5876-6-19 |
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