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Published in: Cancer Immunology, Immunotherapy 1/2013

01-01-2013 | Original article

Increased prevalence of tumor-infiltrating regulatory T cells is closely related to their lower sensitivity to H2O2-induced apoptosis in gastric and esophageal cancer

Authors: Shinichirou Izawa, Kousaku Mimura, Mitsuaki Watanabe, Takanori Maruyama, Yoshihiko Kawaguchi, Hideki Fujii, Koji Kono

Published in: Cancer Immunology, Immunotherapy | Issue 1/2013

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Abstract

Purpose and experimental design

Although an increase in regulatory T cells (Tregs) is observed in tumor microenvironments, the underlying mechanism is not fully clarified. Since it was suggested that Tregs showed a lower sensitivity toward oxidative stress in comparison with conventional T cells, in the present study, we investigated the H2O2 production and apoptosis of Tregs in gastric and esophageal cancer tissues, employing flow cytometric analysis using fresh samples (n = 93) and immunohistochemical analysis (n = 203).

Results

The increased tumor-infiltrating Tregs coexisted with elevated H2O2 production according to disease progression. The grade of apoptosis in Tregs was less pronounced than that in conventional T cells, and there was a positive correlation between H2O2 production and the grade of apoptosis in conventional T cells, while there was no correlation between H2O2 production and the grade of apoptosis in Tregs. Moreover, Tregs were less sensitive to H2O2-induced apoptosis compared with conventional T cells in vitro.

Conclusions

We have demonstrated that the increased prevalence of tumor-infiltrating Tregs closely related to their lower sensitivity to H2O2-induced apoptosis.
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Metadata
Title
Increased prevalence of tumor-infiltrating regulatory T cells is closely related to their lower sensitivity to H2O2-induced apoptosis in gastric and esophageal cancer
Authors
Shinichirou Izawa
Kousaku Mimura
Mitsuaki Watanabe
Takanori Maruyama
Yoshihiko Kawaguchi
Hideki Fujii
Koji Kono
Publication date
01-01-2013
Publisher
Springer-Verlag
Published in
Cancer Immunology, Immunotherapy / Issue 1/2013
Print ISSN: 0340-7004
Electronic ISSN: 1432-0851
DOI
https://doi.org/10.1007/s00262-012-1327-0

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