The role of galectin-3 in cancer drug resistance

被引:141
作者
Fukumori, Tomoharu
Kanayama, Hiro-omi
Raz, Avraham
机构
[1] Wayne State Univ, Karmanos Canc Inst, Tumor Progress & Metastasis Program, Detroit, MI 48201 USA
[2] Univ Tokushima, Grad Sch, Dept Urol, Inst Hlth Biosci, Tokushima 7708503, Japan
关键词
galectin-3; apoptosis; cancer chemotherapy; drug resistance;
D O I
10.1016/j.drup.2007.04.001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The galectins comprise a family of 14 members of beta-galactoside-binding proteins, characterized by their affinity for beta-galactosides and by a conserved sequence in the carbohydrate recognition domain that bind to the carbohydrate portion of cell surface glycoproteins or glycolipids. Galectin-3, a 31 kDa gene product, is a multifunctional oncogenic protein which regulates cell growth, cell adhesion, cell proliferation, angiogenesis, and apoptosis. Recent studies have revealed that galectin-3 demonstrates anti-apoptotic effects which contribute to cell survival in several types of cancer cells. Intracellular galectin-3 in particular, which contains the NWGR anti-death motif of the Bcl-2 family, inhibits cell apoptosis induced by chemotherapeutic agent such as cisplatin and etoposide in some types of cancer cells. We have also reported that nuclear export of phosphorylated galectin-3 regulates its anti-apoptotic activity in response to chemotherapeutic drugs. Here, we will describe the role of galectin-3 as an anti-apoptotic factor in response to chemotherapeutic drugs and will discuss recent data on its molecular mechanism that contribute to drug resistance. We suggest that targeting galectin-3 could improve the efficacy of anticancer drug chemotherapy in several types of cancer. (c) 2007 Published by Elsevier Ltd.
引用
收藏
页码:101 / 108
页数:8
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