Non-histone nuclear factor HMGB1 as a therapeutic target in colorectal cancer

被引:133
作者
Ohmori, Hitoshi [1 ]
Luo, Yi [1 ]
Kuniyasu, Hiroki [1 ]
机构
[1] Nara Med Univ, Dept Mol Pathol, Nara 6348521, Japan
基金
日本学术振兴会;
关键词
AGE; colorectal cancer; HMGB1; macrophage; metastasis; RAGE; GLYCATION END-PRODUCTS; SQUAMOUS-CELL CARCINOMA; GROUP BOX 1; MELANOMA INHIBITORY-ACTIVITY; DOWN-REGULATES HMGB1; COLON-CANCER; NEURITE OUTGROWTH; BINDING-PROTEINS; PROSTATE-CANCER; DENDRITIC CELLS;
D O I
10.1517/14728222.2011.546785
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Introduction: High-motility group box (HMGB)-1 is the focus of recent cancer research. HMGB1 plays a critical role in cancer development, progression, and metastasis by activation of cancer cells, enhancement of tumor angiogenesis, and suppression of host anti-cancer immunity. HMGB1 is a relevant target for cancer treatment. Areas covered: This review aims to overview the biological feature and diverses role in cancer of HMGB1. HMGB1 is a non-histone chromosomal protein, a secretory protein binding to the receptor for advanced glycation end products in cancer cells andmonocyte-lineage immune cells, and a DNA presenting chaperon for toll-like receptors. HMGB1 enhances proliferation, motility, invasion and survival of cancer cells. In contrast, HMGB1 induces apoptosis in monocyte-lineage immune cells and inhibits tumor-infiltrating macrophages and dendritic cells, lymph node sinus macrophages and liver Kupffer cells to attenuate anti-cancer immune responses and anti-metastatic organ defense. Then the novel techniques for inhibiting HMGB1 are reviewed. Expert opinion: Various techniques targeting HMGB1 are subjected to trial. HMGB1 targeting is a potential therapeutic techniqueagainst cancer development, progression, and especially metastasis. Technical breakthroughs in application of HMGB1 targeting to human diseases are now urgently required.
引用
收藏
页码:183 / 193
页数:11
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