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The Exceptional Oncogenicity of HTLV-1
Human T-cell leukemia virus-1 (HTLV-1) is the first pathogenic human retrovirus identified in 1979 by the Gallo group. HTLV-1 causes fatal T-cell leukemia (adult T cell leukemia) and a progressive myelopahy (HTLV-1-associated myelopathy/ tropical spastic paraparesis, HAM/TSP) and other disorders. Si...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5539117/ https://www.ncbi.nlm.nih.gov/pubmed/28824561 http://dx.doi.org/10.3389/fmicb.2017.01425 |
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author | Tagaya, Yutaka Gallo, Robert C. |
author_facet | Tagaya, Yutaka Gallo, Robert C. |
author_sort | Tagaya, Yutaka |
collection | PubMed |
description | Human T-cell leukemia virus-1 (HTLV-1) is the first pathogenic human retrovirus identified in 1979 by the Gallo group. HTLV-1 causes fatal T-cell leukemia (adult T cell leukemia) and a progressive myelopahy (HTLV-1-associated myelopathy/ tropical spastic paraparesis, HAM/TSP) and other disorders. Since the discovery of HTLV-1, several other microorganisms are demonstrated to cause cancer in humans. In this article, we investigated the oncogenic capacity of HTLV-1, in comparison with those of other oncoviruses and one oncobacterium (Helicobacter pylori, H. Pylori) based on published literature. We conclude here that HTLV-1 is one of the most and may be the most carcinogenic among them and arguably one of the most potent of the known human carcinogens. This fact has not been noted before and is particularly important to justify why we need to study HTLV-1 as an important model of human viral oncogenesis. |
format | Online Article Text |
id | pubmed-5539117 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-55391172017-08-18 The Exceptional Oncogenicity of HTLV-1 Tagaya, Yutaka Gallo, Robert C. Front Microbiol Microbiology Human T-cell leukemia virus-1 (HTLV-1) is the first pathogenic human retrovirus identified in 1979 by the Gallo group. HTLV-1 causes fatal T-cell leukemia (adult T cell leukemia) and a progressive myelopahy (HTLV-1-associated myelopathy/ tropical spastic paraparesis, HAM/TSP) and other disorders. Since the discovery of HTLV-1, several other microorganisms are demonstrated to cause cancer in humans. In this article, we investigated the oncogenic capacity of HTLV-1, in comparison with those of other oncoviruses and one oncobacterium (Helicobacter pylori, H. Pylori) based on published literature. We conclude here that HTLV-1 is one of the most and may be the most carcinogenic among them and arguably one of the most potent of the known human carcinogens. This fact has not been noted before and is particularly important to justify why we need to study HTLV-1 as an important model of human viral oncogenesis. Frontiers Media S.A. 2017-08-02 /pmc/articles/PMC5539117/ /pubmed/28824561 http://dx.doi.org/10.3389/fmicb.2017.01425 Text en Copyright © 2017 Tagaya and Gallo. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Tagaya, Yutaka Gallo, Robert C. The Exceptional Oncogenicity of HTLV-1 |
title | The Exceptional Oncogenicity of HTLV-1 |
title_full | The Exceptional Oncogenicity of HTLV-1 |
title_fullStr | The Exceptional Oncogenicity of HTLV-1 |
title_full_unstemmed | The Exceptional Oncogenicity of HTLV-1 |
title_short | The Exceptional Oncogenicity of HTLV-1 |
title_sort | exceptional oncogenicity of htlv-1 |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5539117/ https://www.ncbi.nlm.nih.gov/pubmed/28824561 http://dx.doi.org/10.3389/fmicb.2017.01425 |
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