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TOX Acts an Oncological Role in Mycosis Fungoides

Mycosis fungoides (MF) is a low-grade lymphoma characterized by clonal expansion of atypical CD4+ skin-homing T lymphocytes. Herein, we examined the role of thymocytes selection associated HMG-box (TOX), a gene previously found to be unregulated in MF skin biopsies, in MF pathogenesis. TOX encodes a...

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Detalles Bibliográficos
Autores principales: Yu, Xin, Luo, Yixin, Liu, Jie, Liu, Yuehua, Sun, Qiuning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4374776/
https://www.ncbi.nlm.nih.gov/pubmed/25811617
http://dx.doi.org/10.1371/journal.pone.0117479
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author Yu, Xin
Luo, Yixin
Liu, Jie
Liu, Yuehua
Sun, Qiuning
author_facet Yu, Xin
Luo, Yixin
Liu, Jie
Liu, Yuehua
Sun, Qiuning
author_sort Yu, Xin
collection PubMed
description Mycosis fungoides (MF) is a low-grade lymphoma characterized by clonal expansion of atypical CD4+ skin-homing T lymphocytes. Herein, we examined the role of thymocytes selection associated HMG-box (TOX), a gene previously found to be unregulated in MF skin biopsies, in MF pathogenesis. TOX encodes a high-mobility group family (HMG) domain DNA binding nuclear protein, which regulates the differentiation of developing T-cells. First, we confirmed that TOX expression levels in MF were increased compared with those in benign inflammatory dermatitis (BID) and normal skin. In addition, TOX level increased with the progression MF from patch stage to tumor stage. Overexpression of TOX accelerated the proliferation and migration of MF cell lines in vitro, which were blocked by AKT inhibitors. In conclusion, our study confirmed that TOX was highly expressed in MF lesions and accelerates the proliferation and migration of MF. TOX is a diagnostic marker for MF and may play a pathogenic role in disease progression.
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spelling pubmed-43747762015-04-04 TOX Acts an Oncological Role in Mycosis Fungoides Yu, Xin Luo, Yixin Liu, Jie Liu, Yuehua Sun, Qiuning PLoS One Research Article Mycosis fungoides (MF) is a low-grade lymphoma characterized by clonal expansion of atypical CD4+ skin-homing T lymphocytes. Herein, we examined the role of thymocytes selection associated HMG-box (TOX), a gene previously found to be unregulated in MF skin biopsies, in MF pathogenesis. TOX encodes a high-mobility group family (HMG) domain DNA binding nuclear protein, which regulates the differentiation of developing T-cells. First, we confirmed that TOX expression levels in MF were increased compared with those in benign inflammatory dermatitis (BID) and normal skin. In addition, TOX level increased with the progression MF from patch stage to tumor stage. Overexpression of TOX accelerated the proliferation and migration of MF cell lines in vitro, which were blocked by AKT inhibitors. In conclusion, our study confirmed that TOX was highly expressed in MF lesions and accelerates the proliferation and migration of MF. TOX is a diagnostic marker for MF and may play a pathogenic role in disease progression. Public Library of Science 2015-03-26 /pmc/articles/PMC4374776/ /pubmed/25811617 http://dx.doi.org/10.1371/journal.pone.0117479 Text en © 2015 Yu et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
spellingShingle Research Article
Yu, Xin
Luo, Yixin
Liu, Jie
Liu, Yuehua
Sun, Qiuning
TOX Acts an Oncological Role in Mycosis Fungoides
title TOX Acts an Oncological Role in Mycosis Fungoides
title_full TOX Acts an Oncological Role in Mycosis Fungoides
title_fullStr TOX Acts an Oncological Role in Mycosis Fungoides
title_full_unstemmed TOX Acts an Oncological Role in Mycosis Fungoides
title_short TOX Acts an Oncological Role in Mycosis Fungoides
title_sort tox acts an oncological role in mycosis fungoides
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4374776/
https://www.ncbi.nlm.nih.gov/pubmed/25811617
http://dx.doi.org/10.1371/journal.pone.0117479
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