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Review

High Mobility Group Box 1 in Human Cancer

1
Department of Immunology, Faculty of Health Sciences, University of Pretoria, Pretoria 0001, South Africa
2
The Medical Oncology Centre of Rosebank, Johannesburg 2196, South Africa
3
The Breast Care Centre, Netcare Milpark, 9 Guild Road, Parktown, Johannesburg 2193, South Africa
*
Author to whom correspondence should be addressed.
Cells 2020, 9(7), 1664; https://doi.org/10.3390/cells9071664
Submission received: 28 May 2020 / Revised: 3 July 2020 / Accepted: 6 July 2020 / Published: 10 July 2020
(This article belongs to the Special Issue HMGB1 in Health and Disease)

Abstract

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.
Keywords: cytokines; immunosuppression; myeloid-derived suppressor cells; prognostic factor; receptor for advanced glycation end-products; redox isoforms; Toll-like receptors; tumor microenvironment; T regulatory cells; tumorigenesis cytokines; immunosuppression; myeloid-derived suppressor cells; prognostic factor; receptor for advanced glycation end-products; redox isoforms; Toll-like receptors; tumor microenvironment; T regulatory cells; tumorigenesis

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MDPI and ACS Style

Rapoport, B.L.; Steel, H.C.; Theron, A.J.; Heyman, L.; Smit, T.; Ramdas, Y.; Anderson, R. High Mobility Group Box 1 in Human Cancer. Cells 2020, 9, 1664. https://doi.org/10.3390/cells9071664

AMA Style

Rapoport BL, Steel HC, Theron AJ, Heyman L, Smit T, Ramdas Y, Anderson R. High Mobility Group Box 1 in Human Cancer. Cells. 2020; 9(7):1664. https://doi.org/10.3390/cells9071664

Chicago/Turabian Style

Rapoport, Bernardo L., Helen C. Steel, Annette J. Theron, Liezl Heyman, Teresa Smit, Yastira Ramdas, and Ronald Anderson. 2020. "High Mobility Group Box 1 in Human Cancer" Cells 9, no. 7: 1664. https://doi.org/10.3390/cells9071664

APA Style

Rapoport, B. L., Steel, H. C., Theron, A. J., Heyman, L., Smit, T., Ramdas, Y., & Anderson, R. (2020). High Mobility Group Box 1 in Human Cancer. Cells, 9(7), 1664. https://doi.org/10.3390/cells9071664

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