Glycosylation of ceramide potentiates cellular resistance to tumor necrosis factor-α-induced apoptosis

被引:71
作者
Liu, YY
Han, TY
Giuliano, AE
Ichikawa, S
Hirabayashi, Y
Cabot, MC
机构
[1] St Johns Hlth Ctr, John Wayne Canc Inst, Santa Monica, CA 90404 USA
[2] RIKEN, Inst Phys & Chem Res, Lab Cellular Glycobiol, Wako, Saitama, Japan
关键词
tumor necrosis factor-alpha; ceramide; glycosylation; drug resistance; breast cancer;
D O I
10.1006/excr.1999.4649
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Ceramide, as a second messenger, initiates one of the major signal transduction pathways in tumor necrosis factor-alpha (TNF-alpha)-induced apoptosis. Glucosylceramide synthase (GCS) catalyzes glycosylation of ceramide and produces glucosylceramide. By introduction of the GCS gene, cytotoxic resistance to TNF-alpha has been conferred in human breast cancer cells. MCF-7/GCS-transfected cells expressed 4.1-fold higher levels of GCS activity and exhibited a 15-fold (P < 0.0005) greater EC50 for TNF-alpha compared with the parental MCF-7 cell line. DNA fragmentation and DNA synthesis studies showed that TNF-alpha had little influence on the induction of apoptosis or on growth arrest in MCF-7/GCS cells, compared to MCF-7 cells. These studies reveal that TNF-alpha resistance in MCF-7/GCS cells is closely related to ceramide hyperglycosylation, a hallmark of this transfected cell line, and resistance was not aligned with changes in TNF receptor 1 expression. This work demonstrates that GCS, which catalyzes ceramide glycosylation, potentiates cytotoxic resistance to TNF-alpha. (C) 1998 Academic Press.
引用
收藏
页码:464 / 470
页数:7
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