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Published in: Cancer Immunology, Immunotherapy 3/2013

01-03-2013 | Original article

Up-regulation of Foxp3 participates in progression of cervical cancer

Authors: Chao Zeng, Yunhong Yao, Wei Jie, Miao Zhang, Xinrong Hu, Yi Zhao, Sen Wang, Jinbao Yin, Yulan Song

Published in: Cancer Immunology, Immunotherapy | Issue 3/2013

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Abstract

Foxp3 was identified as a key protein in mediating inhibitory functions of regulatory T cell (Treg). Foxp3 was thought to express only in the T cell lineage until recently when some researches reported that Foxp3 was also expressed by cancer cells. In this study, we describe for the first time the expression of Foxp3 in cervical cancer. Progression from cervical intraepithelial neoplasia (CIN) to cervical cancer is a multistep process initiated by persistent infection with high-risk human papillomavirus (HPV). P16INK4a is a crucial marker of HPV integration into host cells. In the present study, expressions of Foxp3 and P16INK4a in CIN and cervical cancer were detected by immunohistochemistry. Our results found expression level of Foxp3 was increased during the progression of cervical neoplasia. Moreover, up-regulation of Foxp3 appeared to be correlated with the expression of P16INK4a. Examination of the role of Foxp3 in differentiation by double immunostaining for cytokeratin 10 (CK10) showed significant association between Foxp3 expression and differentiation (Foxp3 vs CK10). Furthermore, positive expression of Foxp3 was correlated with tumor size. These data suggest that Foxp3 may play an important role in differentiation and growth of cervical cancer cells. Our findings provide new insights regarding the role of Foxp3 in differentiation and its association with HPV infection during the development of cervical cancer.
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Metadata
Title
Up-regulation of Foxp3 participates in progression of cervical cancer
Authors
Chao Zeng
Yunhong Yao
Wei Jie
Miao Zhang
Xinrong Hu
Yi Zhao
Sen Wang
Jinbao Yin
Yulan Song
Publication date
01-03-2013
Publisher
Springer-Verlag
Published in
Cancer Immunology, Immunotherapy / Issue 3/2013
Print ISSN: 0340-7004
Electronic ISSN: 1432-0851
DOI
https://doi.org/10.1007/s00262-012-1348-8

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