Nuclear transport of galectin-3 and its therapeutic implications

被引:63
作者
Funasaka, Tatsuyoshi [1 ]
Raz, Avraham [2 ]
Nangia-Makker, Pratima [3 ,4 ]
机构
[1] Nanzando Pharmacies Co, Minato Ku, Tokyo 1080074, Japan
[2] Wayne State Univ, Dept Oncol, Sch Med, Detroit, MI 48202 USA
[3] Wayne State Univ, Sch Med, Dept Internal Med, Detroit, MI 48202 USA
[4] John D Dingell VA Med Ctr, Detroit, MI 48201 USA
基金
美国国家卫生研究院;
关键词
Galectin-3; Nuclear cytoplasmic transport; Beta catenin; GLYCOGEN-SYNTHASE KINASE-3-BETA; CARBOHYDRATE-BINDING PROTEIN-35; BETA-CATENIN TRANSACTIVATION; SQUAMOUS-CELL CARCINOMA; PORE COMPLEX STRUCTURE; WNT SIGNALING PATHWAY; BREAST-CANCER; PROSTATE-CANCER; DRUG-RESISTANCE; CITRUS PECTIN;
D O I
10.1016/j.semcancer.2014.03.004
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Galectin-3, a member of beta-galactoside-binding gene family is a multi-functional protein, which regulates pleiotropic biological functions such as cell growth, cell adhesion, cell-cell interactions, apoptosis, angiogenesis and mRNA processing. Its unique structure enables it to interact with a plethora of ligands in a carbohydrate dependent or independent manner. Galectin-3 is mainly a cytosolic protein, but can easily traverse the intracellular and plasma membranes to translocate into the nucleus, mitochondria or get externalized. Depending on the cell type, specific experimental conditions in vitro, cancer type and stage, galectin-3 has been reported to be exclusively cytoplasmic, predominantly nuclear or distributed between the two compartments. In this review we have summarized the dynamics of galectin-3 shuttling between the nucleus and the cytoplasm, the nuclear transport mechanisms of galectin-3, how its specific interactions with the members of beta-catenin signaling pathways affect tumor progression, and its implications as a therapeutic target. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:30 / 38
页数:9
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