Sphingolipid targets in cancer therapy

被引:122
作者
Modrak, DE [1 ]
Gold, DV [1 ]
Goldenberg, DM [1 ]
机构
[1] Garden State Canc Ctr, Ctr Mol Med & Immunol, Belleville, NJ 07109 USA
关键词
D O I
10.1158/1535-7163.MCT-05-0420
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Considerable progress has been made recently in our understanding of the role of ceramide in the induction of apoptotic cell death. Ceramide is produced by cancer cells in response to exposure to radiation and most chemotherapeutics and is an intracellular second messenger that activates enzymes, leading to apoptosis. Because of its central role in apoptosis, pharmacologic manipulation of intracellular ceramide levels should result in attenuation or enhancement of drug resistance. This may be achieved through direct application of sphingolipids or by the inhibition/activation of the enzymes that either produce or use ceramide. In addition attention should be given to the subcellular location of ceramide generation, because this has been shown to affect the biological activity of sphingolipids. This review summarizes the sphingolipid biosynthetic pathway, as it relates to the identification of important targets for drug discovery, and the development of novel agents capable of enhancing chemotherapy.
引用
收藏
页码:200 / 208
页数:9
相关论文
共 73 条
[1]   Phospholipids and nuclear RNA [J].
Albi, E ;
Micheli, M ;
Magni, MPV .
CELL BIOLOGY INTERNATIONAL, 1996, 20 (06) :407-412
[2]   RESYNTHESIS OF SPHINGOMYELIN FROM PLASMA-MEMBRANE PHOSPHATIDYLCHOLINE IN BHK CELLS TREATED WITH STAPHYLOCOCCUS-AUREUS SPHINGOMYELINASE [J].
ALLAN, D ;
QUINN, P .
BIOCHEMICAL JOURNAL, 1988, 254 (03) :765-771
[3]   Ceramide in apoptosis signaling:: Relationship with oxidative stress [J].
Andrieu-Abadie, N ;
Gouazé, V ;
Salvayre, R ;
Levade, T .
FREE RADICAL BIOLOGY AND MEDICINE, 2001, 31 (06) :717-728
[4]   (1S,2R)-D-erythro-2-(N-myristoylamino)-1-phenyl-1-propanol as an inhibitor of ceramidase [J].
Bielawska, A ;
Greenberg, MS ;
Perry, D ;
Jayadev, S ;
Shayman, JA ;
McKay, C ;
Hannun, YA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (21) :12646-12654
[5]   Mitochondria and ceramide: intertwined roles in regulation of apoptosis [J].
Birbes, H ;
El Bawab, S ;
Obeid, LM ;
Hannun, YA .
ADVANCES IN ENZYME REGULATION, VOL 42, PROCEEDINGS, 2002, 42 :113-129
[6]   Selective hydrolysis of a mitochondrial pool of sphingomyelin induces apoptosis [J].
Birbes, H ;
El Bawab, S ;
Hannun, YA ;
Obeid, LM .
FASEB JOURNAL, 2001, 15 (14) :2669-2679
[7]   Glucosylceramide synthase and apoptosis [J].
Bleicher, RJ ;
Cabot, MC .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 2002, 1585 (2-3) :172-178
[8]   CERAMIDE SYNTHASE MEDIATES DAUNORUBICIN-INDUCED APOPTOSIS - AN ALTERNATIVE MECHANISM FOR GENERATING DEATH SIGNALS [J].
BOSE, R ;
VERHEIJ, M ;
HAIMOVITZFRIEDMAN, A ;
SCOTTO, K ;
FUKS, Z ;
KOLESNICK, R .
CELL, 1995, 82 (03) :405-414
[9]  
BOUDKER O, 1993, J BIOL CHEM, V268, P22150
[10]   FTY720, a new class of immunomodulator, inhibits lymphocyte egress from secondary lymphoid tissues and thymus by agonistic activity at sphingosine 1-phosphate receptors [J].
Chiba, K .
PHARMACOLOGY & THERAPEUTICS, 2005, 108 (03) :308-319