Human β-galactoside α-2,3-sialyltransferase (ST3Gal III) attenuated Taxol-induced apoptosis in ovarian cancer cells by downregulating caspase-8 activity

被引:20
|
作者
Huang, Su [1 ]
Day, Travis W. [1 ]
Choi, Mi-Ran [1 ]
Safa, Ahmad R. [1 ]
机构
[1] Indiana Univ, Dept Pharmacol & Toxicol, Simon Canc Ctr, Sch Med, Indianapolis, IN 46202 USA
关键词
Taxol; ST3Gal III; Sialyltransferases; Apoptosis; Caspase-8; Sialylation; Ovarian cancer; SIALYLTRANSFERASE FAMILY MEMBERS; PACLITAXEL-INDUCED APOPTOSIS; HUMAN SKOV3 OVARIAN; BREAST-CANCER; CARCINOMA CELLS; LUNG-CANCER; GLYCOSYLATION; EXPRESSION; PROTEINS; TRANSCRIPTION;
D O I
10.1007/s11010-009-0147-9
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Taxol triggers apoptosis in a variety of cancer cells, but it also upregulates cytoprotective proteins and/or pathways that compromise its therapeutic efficacy. In this report, we found that Taxol treatment resulted in caspase-8-dependent apoptosis in SKOV3 human ovarian cancer cells. Moreover, Taxol-induced apoptosis was associated with caspase-3 activation. Interestingly, Taxol treatment upregulated alpha-2,3-sialyltransferase (ST3Gal III) expression and forced expression of ST3Gal III attenuated Taxol-induced apoptosis. Furthermore, ST3Gal III overexpression inhibited Taxol-triggered caspase-8 activation, indicating that ST3Gal III upregulation produces cellular resistance to Taxol and hence reduces the efficacy of Taxol therapy.
引用
收藏
页码:81 / 88
页数:8
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