Toxicity of fatty acids on murine and human melanoma cell lines

被引:75
作者
Andrade, LND
de Lima, TM
Curi, R
Castrucci, AMD
机构
[1] Univ Sao Paulo, Inst Ciencias Biomed, Dept Fisiol & Biofis, Sao Paulo, Brazil
[2] Univ Sao Paulo, Inst Biociencias, Dept Fisiol, Sao Paulo, Brazil
[3] Uniformed Serv Univ Hlth Sci, Dept Anat Physiol & Genet, Bethesda, MD 20814 USA
基金
巴西圣保罗研究基金会;
关键词
palmitic acid; arachidonic acid; linoleic acid; toxicity; melanoma cells; cell death;
D O I
10.1016/j.tiv.2005.02.002
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
High concentrations of certain fatty acids can cause cell death via apoptosis or necrosis. The aim of this study was to investigate the toxicity of saturated and unsaturated fatty acids on melanoma cell lines, which was evaluated by either loss of membrane integrity and/or DNA fragmentation using flow cytometric analysis. Evidence is presented that saturated and unsaturated fatty acids exert toxic effects on melanoma cells through loss of membrane integrity and/or DNA fragmentation. Arachidonic and linoleic acids were the most effective in decreasing the number of viable S91 murine melanoma cells, causing loss of membrane integrity and DNA fragmentation at 100 mu M concentration already after 24 h in culture. In B16F 10 murine melanoma cells, palmitic acid was the most toxic, inducing cell death by both apoptosis and necrosis. The human melanoma cell lines were more resistant to the toxic effect of fatty acids. In SK-Mel 23 cells, indications of cytotoxicity were detected only after 48 h treatment with arachidonic, linoleic, palmitic and palmitoleic acids at 200 mu M concentration. Linoleic acid was the most toxic for this cell line. In SK-Mel 28 human cells, only palmitic acid caused a significant decrease of the number of viable cells, inducing DNA fragmentation after 24 and 48 h treatments at 200 mu M concentration. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:553 / 560
页数:8
相关论文
共 49 条
  • [21] Herbst U, 1999, J CELL PHYSIOL, V181, P295, DOI 10.1002/(SICI)1097-4652(199911)181:2<295::AID-JCP11>3.3.CO
  • [22] 2-9
  • [23] HERLYN M, 2001, CANC PRINCIPLES PRAC
  • [24] Ranking the toxicity of fatty acids on Jurkat and Raji cells by flow cytometric analysis
    Lima, TM
    Kanunfre, CC
    Pompéia, C
    Verlengia, R
    Curi, R
    [J]. TOXICOLOGY IN VITRO, 2002, 16 (06) : 741 - 747
  • [25] Palmitate-induced apoptosis can occur through a ceramide-independent pathway
    Listenberger, LL
    Ory, DS
    Schaffer, JE
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (18) : 14890 - 14895
  • [26] EFFECTS OF EICOSAPENTAENOIC ACID, GAMMA-LINOLENIC ACID AND PROSTAGLANDIN-E1 ON 3 HUMAN COLON-CARCINOMA CELL-LINES
    MENGEAUD, V
    NANO, JL
    FOURNEL, S
    RAMPAL, P
    [J]. PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS, 1992, 47 (04): : 313 - 319
  • [27] Analysis of the cytotoxic properties of linoleic acid metabolites produced by renal and hepatic P450s
    Moran, JH
    Mitchell, LA
    Bradbury, JA
    Qu, W
    Zeldin, DC
    Schnellmann, RG
    Grant, DF
    [J]. TOXICOLOGY AND APPLIED PHARMACOLOGY, 2000, 168 (03) : 268 - 279
  • [28] Saturated FFAs, palmitic acid and stearic acid, induce apoptosis in human granulosa cells
    Mu, YM
    Yanase, T
    Nishi, Y
    Tanaka, A
    Saito, M
    Jin, CH
    Mukasa, C
    Okabe, T
    Nomura, M
    Goto, K
    Nawata, H
    [J]. ENDOCRINOLOGY, 2001, 142 (08) : 3590 - 3597
  • [29] A RAPID AND SIMPLE METHOD FOR MEASURING THYMOCYTE APOPTOSIS BY PROPIDIUM IODIDE STAINING AND FLOW-CYTOMETRY
    NICOLETTI, I
    MIGLIORATI, G
    PAGLIACCI, MC
    GRIGNANI, F
    RICCARDI, C
    [J]. JOURNAL OF IMMUNOLOGICAL METHODS, 1991, 139 (02) : 271 - 279
  • [30] NOGUCHI M, 1995, ONCOLOGY, V52, P458