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High Mobility Group Box 1 in Human Cancer
High mobility group box 1 (HMGB1) is an extremely versatile protein that is located predominantly in the nucleus of quiescent eukaryotic cells, where it is critically involved in maintaining genomic structure and function. During cellular stress, however, this multifaceted, cytokine-like protein und...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7407638/ https://www.ncbi.nlm.nih.gov/pubmed/32664328 http://dx.doi.org/10.3390/cells9071664 |
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author | Rapoport, Bernardo L. Steel, Helen C. Theron, Annette J. Heyman, Liezl Smit, Teresa Ramdas, Yastira Anderson, Ronald |
author_facet | Rapoport, Bernardo L. Steel, Helen C. Theron, Annette J. Heyman, Liezl Smit, Teresa Ramdas, Yastira Anderson, Ronald |
author_sort | Rapoport, Bernardo L. |
collection | PubMed |
description | High mobility group box 1 (HMGB1) is an extremely versatile protein that is located predominantly in the nucleus of quiescent eukaryotic cells, where it is critically involved in maintaining genomic structure and function. During cellular stress, however, this multifaceted, cytokine-like protein undergoes posttranslational modifications that promote its translocation to the cytosol, from where it is released extracellularly, either actively or passively, according to cell type and stressor. In the extracellular milieu, HMGB1 triggers innate inflammatory responses that may be beneficial or harmful, depending on the magnitude and duration of release of this pro-inflammatory protein at sites of tissue injury. Heightened awareness of the potentially harmful activities of HMGB1, together with a considerable body of innovative, recent research, have revealed that excessive production of HMGB1, resulting from misdirected, chronic inflammatory responses, appears to contribute to all the stages of tumorigenesis. In the setting of established cancers, the production of HMGB1 by tumor cells per se may also exacerbate inflammation-related immunosuppression. These pro-inflammatory mechanisms of HMGB1-orchestrated tumorigenesis, as well as the prognostic potential of detection of elevated expression of this protein in the tumor microenvironment, represent the major thrusts of this review. |
format | Online Article Text |
id | pubmed-7407638 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-74076382020-08-12 High Mobility Group Box 1 in Human Cancer Rapoport, Bernardo L. Steel, Helen C. Theron, Annette J. Heyman, Liezl Smit, Teresa Ramdas, Yastira Anderson, Ronald Cells Review High mobility group box 1 (HMGB1) is an extremely versatile protein that is located predominantly in the nucleus of quiescent eukaryotic cells, where it is critically involved in maintaining genomic structure and function. During cellular stress, however, this multifaceted, cytokine-like protein undergoes posttranslational modifications that promote its translocation to the cytosol, from where it is released extracellularly, either actively or passively, according to cell type and stressor. In the extracellular milieu, HMGB1 triggers innate inflammatory responses that may be beneficial or harmful, depending on the magnitude and duration of release of this pro-inflammatory protein at sites of tissue injury. Heightened awareness of the potentially harmful activities of HMGB1, together with a considerable body of innovative, recent research, have revealed that excessive production of HMGB1, resulting from misdirected, chronic inflammatory responses, appears to contribute to all the stages of tumorigenesis. In the setting of established cancers, the production of HMGB1 by tumor cells per se may also exacerbate inflammation-related immunosuppression. These pro-inflammatory mechanisms of HMGB1-orchestrated tumorigenesis, as well as the prognostic potential of detection of elevated expression of this protein in the tumor microenvironment, represent the major thrusts of this review. MDPI 2020-07-10 /pmc/articles/PMC7407638/ /pubmed/32664328 http://dx.doi.org/10.3390/cells9071664 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Rapoport, Bernardo L. Steel, Helen C. Theron, Annette J. Heyman, Liezl Smit, Teresa Ramdas, Yastira Anderson, Ronald High Mobility Group Box 1 in Human Cancer |
title | High Mobility Group Box 1 in Human Cancer |
title_full | High Mobility Group Box 1 in Human Cancer |
title_fullStr | High Mobility Group Box 1 in Human Cancer |
title_full_unstemmed | High Mobility Group Box 1 in Human Cancer |
title_short | High Mobility Group Box 1 in Human Cancer |
title_sort | high mobility group box 1 in human cancer |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7407638/ https://www.ncbi.nlm.nih.gov/pubmed/32664328 http://dx.doi.org/10.3390/cells9071664 |
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