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Multifaceted functions and roles of HBZ in HTLV-1 pathogenesis

Human T cell leukemia virus type 1 (HTLV-1) is an oncogenic retrovirus responsible for the development of adult T-cell leukemia (ATL). Although HTLV-1 harbors an oncogene, tax, that transforms T cells in vitro and induces leukemia in transgenic mice, tax expression is frequently disrupted in ATL, ma...

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Autores principales: Ma, Guangyong, Yasunaga, Jun-ichirou, Matsuoka, Masao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4793531/
https://www.ncbi.nlm.nih.gov/pubmed/26979059
http://dx.doi.org/10.1186/s12977-016-0249-x
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author Ma, Guangyong
Yasunaga, Jun-ichirou
Matsuoka, Masao
author_facet Ma, Guangyong
Yasunaga, Jun-ichirou
Matsuoka, Masao
author_sort Ma, Guangyong
collection PubMed
description Human T cell leukemia virus type 1 (HTLV-1) is an oncogenic retrovirus responsible for the development of adult T-cell leukemia (ATL). Although HTLV-1 harbors an oncogene, tax, that transforms T cells in vitro and induces leukemia in transgenic mice, tax expression is frequently disrupted in ATL, making the oncogenesis of ATL a bit mysterious. The HTLV-1 bZIP factor (HBZ) gene was discovered in 2002 and has been found to promote T-cell proliferation and cause lymphoma in transgenic mice. Thus HBZ has become a novel hotspot of HTLV-1 research. This review summarizes the current findings on HBZ with a special focus on its potential links to the oncogenesis of ATL. We propose viewing HBZ as a critical contributing factor in ATL development.
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spelling pubmed-47935312016-03-16 Multifaceted functions and roles of HBZ in HTLV-1 pathogenesis Ma, Guangyong Yasunaga, Jun-ichirou Matsuoka, Masao Retrovirology Review Human T cell leukemia virus type 1 (HTLV-1) is an oncogenic retrovirus responsible for the development of adult T-cell leukemia (ATL). Although HTLV-1 harbors an oncogene, tax, that transforms T cells in vitro and induces leukemia in transgenic mice, tax expression is frequently disrupted in ATL, making the oncogenesis of ATL a bit mysterious. The HTLV-1 bZIP factor (HBZ) gene was discovered in 2002 and has been found to promote T-cell proliferation and cause lymphoma in transgenic mice. Thus HBZ has become a novel hotspot of HTLV-1 research. This review summarizes the current findings on HBZ with a special focus on its potential links to the oncogenesis of ATL. We propose viewing HBZ as a critical contributing factor in ATL development. BioMed Central 2016-03-15 /pmc/articles/PMC4793531/ /pubmed/26979059 http://dx.doi.org/10.1186/s12977-016-0249-x Text en © Ma et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Ma, Guangyong
Yasunaga, Jun-ichirou
Matsuoka, Masao
Multifaceted functions and roles of HBZ in HTLV-1 pathogenesis
title Multifaceted functions and roles of HBZ in HTLV-1 pathogenesis
title_full Multifaceted functions and roles of HBZ in HTLV-1 pathogenesis
title_fullStr Multifaceted functions and roles of HBZ in HTLV-1 pathogenesis
title_full_unstemmed Multifaceted functions and roles of HBZ in HTLV-1 pathogenesis
title_short Multifaceted functions and roles of HBZ in HTLV-1 pathogenesis
title_sort multifaceted functions and roles of hbz in htlv-1 pathogenesis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4793531/
https://www.ncbi.nlm.nih.gov/pubmed/26979059
http://dx.doi.org/10.1186/s12977-016-0249-x
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