Department of Surgery, University of Pittsburgh Cancer Institute, Hillman Cancer Center, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Clin Cancer Res. 2013 Aug 1;19(15):4046-57. doi: 10.1158/1078-0432.CCR-13-0495. Epub 2013 May 30.
Forty years ago, high mobility group box 1 (HMGB1) was discovered in calf thymus and named according to its electrophoretic mobility in polyacrylamide gels. Now, we know that HMGB1 performs dual functions. Inside the cell, HMGB1 is a highly conserved chromosomal protein acting as a DNA chaperone. Outside of the cell, HMGB1 is a prototypical damage-associated molecular pattern, acting with cytokines, chemokines, and growth factors. During tumor development and in cancer therapy, HMGB1 has been reported to play paradoxical roles in promoting both cell survival and death by regulating multiple signaling pathways, including inflammation, immunity, genome stability, proliferation, metastasis, metabolism, apoptosis, and autophagy. Here, we review the current knowledge of both HMGB1's oncogenic and tumor-suppressive roles and the potential strategies that target HMGB1 for the prevention and treatment of cancer.
四十年前,高迁移率族蛋白 B1(HMGB1)在小牛胸腺中被发现,并因其在聚丙烯酰胺凝胶中的电泳迁移率而得名。现在,我们知道 HMGB1 具有双重功能。在细胞内,HMGB1 是一种高度保守的染色体蛋白,作为 DNA 伴侣发挥作用。在细胞外,HMGB1 是一种典型的损伤相关分子模式,与细胞因子、趋化因子和生长因子一起发挥作用。在肿瘤发展和癌症治疗过程中,HMGB1 被报道通过调节包括炎症、免疫、基因组稳定性、增殖、转移、代谢、细胞凋亡和自噬在内的多种信号通路,在促进细胞存活和死亡方面发挥着矛盾的作用。在这里,我们综述了 HMGB1 的致癌和抑癌作用的最新知识,以及针对 HMGB1 预防和治疗癌症的潜在策略。