High Mobility Group Box 1 in Human Cancer

被引:50
作者
Rapoport, Bernardo L. [1 ,2 ]
Steel, Helen C. [1 ]
Theron, Annette J. [1 ]
Heyman, Liezl [2 ]
Smit, Teresa [2 ]
Ramdas, Yastira [3 ]
Anderson, Ronald [1 ]
机构
[1] Univ Pretoria, Fac Hlth Sci, Dept Immunol, ZA-0001 Pretoria, South Africa
[2] Med Oncol Ctr Rosebank, ZA-2196 Johannesburg, South Africa
[3] Netcare Milpk, Breast Care Ctr, 9 Guild Rd, ZA-2193 Johannesburg, South Africa
关键词
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; CHROMATIN PROTEIN HMGB1; REGULATORY B-CELLS; END-PRODUCTS RAGE; HEPATOCELLULAR-CARCINOMA; SUPPRESSOR-CELLS; TUMOR MICROENVIRONMENT; SIGNALING PATHWAY; CYTOKINE ACTIVITY; DENDRITIC CELLS; COLON-CANCER;
D O I
10.3390/cells9071664
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
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页数:30
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