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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...

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Autores principales: Karanikas, Vaios, Speletas, Matthaios, Zamanakou, Maria, Kalala, Fani, Loules, Gedeon, Kerenidi, Theodora, Barda, Angeliki K, Gourgoulianis, Konstantinos I, Germenis, Anastasios E
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
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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.
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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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