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
相关论文
共 34 条
[21]   Caspase 7-induced cleavage of kinectin in apoptotic cells [J].
Machleidt, T ;
Geller, P ;
Schwandner, R ;
Scherer, G ;
Krönke, M .
FEBS LETTERS, 1998, 436 (01) :51-54
[22]   GLUCOSYLCERAMIDES STIMULATE MURINE EPIDERMAL HYPERPROLIFERATION [J].
MARSH, NL ;
ELIAS, PM ;
HOLLERAN, WM .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 95 (06) :2903-2909
[23]   Role of an acidic compartment in tumor-necrosis-factor-α-induced production of ceramide, activation of caspase-3 and apoptosis [J].
Monney, L ;
Olivier, R ;
Otter, I ;
Jansen, B ;
Poirier, GG ;
Borner, C .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1998, 251 (1-2) :295-303
[24]   Apoptosis by death factor [J].
Nagata, S .
CELL, 1997, 88 (03) :355-365
[25]   Caspases: killer proteases [J].
Nicholson, DW ;
Thornberry, NA .
TRENDS IN BIOCHEMICAL SCIENCES, 1997, 22 (08) :299-306
[26]   Stress-induced apoptosis and the sphingomyelin pathway [J].
Pena, LA ;
Fuks, Z ;
Kolesnick, R .
BIOCHEMICAL PHARMACOLOGY, 1997, 53 (05) :615-621
[27]   CELL-CYCLE ARREST INDUCED BY ALL INHIBITOR OF GLUCOSYLCERAMIDE SYNTHASE - CORRELATION WITH CYCLIN-DEPENDENT KINASES [J].
RANI, CSS ;
ABE, A ;
CHANG, Y ;
ROSENZWEIG, N ;
SALTIEL, AR ;
RADIN, NS ;
SHAYMAN, JA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (06) :2859-2867
[28]   2 TUMOR-NECROSIS-FACTOR RECEPTORS - STRUCTURE AND FUNCTION [J].
VANDENABEELE, P ;
DECLERCQ, W ;
BEYAERT, R ;
FIERS, W .
TRENDS IN CELL BIOLOGY, 1995, 5 (10) :392-399
[29]  
Vieira KBL, 1996, CANCER RES, V56, P2452
[30]   Up-regulation of glucosylceramide synthase expression and activity during human keratinocyte differentiation [J].
Watanabe, R ;
Wu, K ;
Paul, P ;
Marks, DL ;
Kobayashi, T ;
Pittelkow, MR ;
Pagano, RE .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (16) :9651-9655