陈传贵, 于振涛. 抗肿瘤治疗的新靶点—HMGB1[J]. 中国肿瘤临床, 2009, 36(2): 114-117. DOI: 10.3969/j.issn.1000-8179.2009.02.014
引用本文: 陈传贵, 于振涛. 抗肿瘤治疗的新靶点—HMGB1[J]. 中国肿瘤临床, 2009, 36(2): 114-117. DOI: 10.3969/j.issn.1000-8179.2009.02.014
CHEN Chuangui, YU Zhentao. HMGB1: A Potential Target for Tumor Therapy[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2009, 36(2): 114-117. DOI: 10.3969/j.issn.1000-8179.2009.02.014
Citation: CHEN Chuangui, YU Zhentao. HMGB1: A Potential Target for Tumor Therapy[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2009, 36(2): 114-117. DOI: 10.3969/j.issn.1000-8179.2009.02.014

抗肿瘤治疗的新靶点—HMGB1

HMGB1: A Potential Target for Tumor Therapy

  • 摘要: 高迁移率蛋白B1(High-mobility group box-1,HMGB 1)是细胞内的非组蛋白染色体结合蛋白,在维持核小体稳定和DNA重组、复制、修复及基因转录中发挥着重要作用。而细胞外的HMGB 1 可作为一种“晚期炎症介质”,在炎症的晚期阶段启动着炎症反应。最近研究发现,HMGB 1 也高表达于多种肿瘤组织,与其受体结合后,对
    肿瘤新生血管形成和肿瘤细胞的浸润、转移、增殖及凋亡等有着重要的影响。然而,HMGB 1 的表达和功能在某些肿瘤细胞中的表现可能并不一样。由于HMGB 1 与肿瘤细胞的多种生物学特性都密切相关,因此,以HMGB 1 为靶点有望成为抗肿瘤治疗的有效方法之一。尽管,当前人们通过抑制HMGB 1 的表达、分泌、释放、合成及信号传导等措施来进行抗炎症反应已取得了一定的成功,但是,很多措施还没有在抗肿瘤实验中得到应用,尚有待于体内外实验的进一步证实,然而,这些措施将有可能成为抗肿瘤治疗的有效手段。

     

    Abstract: As a nonhistone chromatin-associated protein, high-mobility group box-1 (HMGB1) protein is an intracellular protein that stabilizes nucleosomes and plays a key role in regulating DNA recombination, du-plication, repair and transcription of many genes. Extracellular HMGB 1 acts as a kind of advanced stage medi-ator of inflammation. Recent evidence has revealed that overexpression of HMGB1 in many kinds of tumor, particularly in conjunction with its receptor, has been associated with tumor neoangiogenesis as well as infiltra-tion, metastasis, proliferation and apoptosis of tumor cells. However, the expression and function of HMGB 1 in different tumor cells may be different. Because the biological characteristics of tumor cells are closely relat -ed to the overexpression of HMGB 1, HMGB 1 can be a target for genetic and pharmacological therapy. Re-cently, it was reported that inhibiting the expression, secretion, release, synthesis and signaling pathway of HMGB1 resulted in the arrest of inflammation. These findings warrant application and verification in cancer re -search and may be helpful for developing new treatment strategies for cancer.

     

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