Biologically active sphingolipids in cancer pathogenesis and treatment

被引:1036
作者
Ogretmen, B
Hannun, YA
机构
[1] Med Univ S Carolina, Dept Biochem & Mol Biol, Charleston, SC 29425 USA
[2] Hollings Canc Ctr, Charleston, SC 29425 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1038/nrc1411
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Biologically active sphingolipids have key roles in the regulation of several fundamental biological processes that are integral to cancer pathogenesis. Recent significant progress in understanding biologically active sphingolipid synthesis, specifically within ceramide and sphingosine-1-phosphate (S1P)-mediated pathways, has identified crucial roles for these molecules both in cancer development and progression. Ceramide - a central molecule in sphingolipid metabolism - in effect functions as a tumour-suppressor lipid, inducing antiproliferative and apoptotic responses in various cancer cells. Conversely, S1P induces responses that, on aggregate, render S1P a tumour-promoting lipid. These discoveries are paving the way for the advancement of anticancer therapies.
引用
收藏
页码:604 / 616
页数:13
相关论文
共 131 条
  • [1] Modulating sphingolipid biosynthetic pathway rescues photoreceptor degeneration
    Acharya, U
    Patel, S
    Koundakjian, E
    Nagashima, K
    Han, X
    Acharya, JK
    [J]. SCIENCE, 2003, 299 (5613) : 1740 - 1743
  • [2] Overcoming resistance to γ-rays in squamous carcinoma cells by poly-drug elevation of ceramide levels
    Alphonse, G
    Bionda, C
    Aloy, MT
    Ardail, D
    Rousson, R
    Rodriguez-Lafrasse, C
    [J]. ONCOGENE, 2004, 23 (15) : 2703 - 2715
  • [3] Ceramide in apoptosis signaling:: Relationship with oxidative stress
    Andrieu-Abadie, N
    Gouazé, V
    Salvayre, R
    Levade, T
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 2001, 31 (06) : 717 - 728
  • [4] Induction of apoptosis in human bladder cancer cells in vitro and in vivo caused by FTY720 treatment
    Azuma, H
    Takahara, S
    Horie, S
    Muto, S
    Otsuki, Y
    Katsuoka, Y
    [J]. JOURNAL OF UROLOGY, 2003, 169 (06) : 2372 - 2377
  • [5] AZUMA H, CANC RES, V62, P1410
  • [6] Oxidative stress-induced activation of Lyn recruits sphingomyelinase and is requisite for its stimulation by Ara-C
    Bezombes, C
    Plo, I
    Mas, WMD
    Quillet-Mary, A
    Nègre-Salvayre, A
    Laurent, G
    Jaffrézou, JP
    [J]. FASEB JOURNAL, 2001, 15 (07) : 1583 - +
  • [7] N-acylated serinol is a novel ceramide mimic inducing apoptosis in neuroblastoma cells
    Bieberich, E
    Kawaguchi, T
    Yu, RK
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (01) : 177 - 181
  • [8] Synthesis and characterization of novel ceramide analogs for induction of apoptosis in human cancer cells
    Bieberich, E
    Hu, B
    Silva, J
    MacKinnon, S
    Yu, RK
    Fillmore, H
    Broaddus, WC
    Ottenbrite, RM
    [J]. CANCER LETTERS, 2002, 181 (01) : 55 - 64
  • [9] Phosphorylation of the immunomodulatory drug FTY720 by sphingosine kinases
    Billich, A
    Bornancin, F
    Dévay, P
    Mechtcheriakova, D
    Urtz, N
    Baumruker, T
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (48) : 47408 - 47415
  • [10] Changes in ceramide and sphingomyelin following fludarabine treatment of human chronic B-cell leukemia cells
    Biswal, SS
    Datta, K
    Acquaah-Mensah, GK
    Kehrer, JP
    [J]. TOXICOLOGY, 2000, 154 (1-3) : 45 - 53