Multiplication and death-type of leukemia cell lines exposed to very long-chain polyunsaturated fatty acids

被引:83
作者
Finstad, HS
Myhrstad, MCW
Heimli, H
Lomo, J
Blomhoff, HK
Kolset, SO
Drevon, CA
机构
[1] Univ Oslo, Inst Nutr Res, N-0316 Oslo, Norway
[2] Norwegian Radium Hosp, Inst Canc Res, Dept Immunol, Oslo, Norway
关键词
leukemia cells; arachidonic acid; eicosapentaenoic acid; docosahexaenoic acid; apoptosis; necrosis;
D O I
10.1038/sj.leu.2401030
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Polyunsaturated fatty acids (PUFA) may reduce cell multiplication in cultures of normal, as well as transformed, white blood cells. We assessed the sensitivity of 14 different leukemia cell lines to PUFA by measuring cell number after 3 days of incubation. Ten of the examined cell lines were sensitive to 30, 60 and/or 120 mu M of arachidonic, eicosapentaenoic and docosahexaenoic acid, whereas four cell lines were resistant. The sensitivity to PUFA was not associated with any particular cell lineage, clinical origin or specific mRNA pattern of bcl-2 and c-myc. Effects on cell viability were assessed by studying cell membrane integrity, DNA fragmentation and cell morphology. The sensitive cell lines Raji and Ramos died by necrosis and apoptosis, respectively, during incubation with eicosapentaenoic acid, whereas the viability of the resistant U-698 cell line was unaffected. The effects of EPA on Raji cells, was counteracted by vitamin E, indicating that lipid peroxidation was involved. However, apoptosis induced by eicosapentaenoic acid in Ramos cells, was unaffected by vitamin E, as well as eicosanoid synthesis inhibitors. In conclusion, our results indicate that a majority of leukemia cell lines are sensitive to PUFA. This sensitivity may be caused by induction of apoptosis or necrosis by very long-chain polyunsaturated fatty acids.
引用
收藏
页码:921 / 929
页数:9
相关论文
共 51 条
[1]  
ANEL A, 1992, LEUKEMIA, V6, P680
[2]   EFFECTS OF DIFFERENT DOSES OF FISH-OIL ON RECTAL CELL-PROLIFERATION IN PATIENTS WITH SPORADIC COLONIC ADENOMAS [J].
ANTI, M ;
ARMELAO, F ;
MARRA, G ;
PERCESEPE, A ;
BARTOLI, GM ;
PALOZZA, P ;
PARRELLA, P ;
CANETTA, C ;
GENTILONI, N ;
DEVITIS, I ;
GASBARRINI, G .
GASTROENTEROLOGY, 1994, 107 (06) :1709-1718
[3]  
CALDER PC, 1992, IMMUNOLOGY, V75, P108
[4]   FISH, N-3 FATTY-ACIDS AND HUMAN COLORECTAL AND BREAST-CANCER MORTALITY [J].
CAYGILL, CPJ ;
HILL, MJ .
EUROPEAN JOURNAL OF CANCER PREVENTION, 1995, 4 (04) :329-332
[5]   INFLUENCE OF N-3 FATTY-ACIDS ON THE GROWTH OF HUMAN BREAST-CANCER CELLS IN-VITRO - RELATIONSHIP TO PEROXIDES AND VITAMIN-E [J].
CHAJES, V ;
SATTLER, W ;
STRANZL, A ;
KOSTNER, GM .
BREAST CANCER RESEARCH AND TREATMENT, 1995, 34 (03) :199-212
[6]   Activation of the STAT signaling pathway can cause expression of caspase 1 and apoptosis [J].
Chin, YE ;
Kitagawa, M ;
Kuida, K ;
Flavell, RA ;
Fu, XY .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (09) :5328-5337
[7]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[8]   SUPPRESSION OF GROWTH IN A LEUKEMIC T-CELL LINE BY N-3 AND N-6 POLY-UNSATURATED FATTY-ACIDS [J].
CHOW, SC ;
SISFONTES, L ;
BJORKHEM, I ;
JONDAL, M .
LIPIDS, 1989, 24 (08) :700-704
[9]   Suppression of tumor necrosis factor-induced cell death by inhibitor of apoptosis c-IAP2 is under NF-kappa B control [J].
Chu, ZL ;
McKinsey, TA ;
Liu, L ;
Gentry, JJ ;
Malim, MH ;
Ballard, DW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (19) :10057-10062
[10]   INTERNUCLEOSOMAL DNA CLEAVAGE SHOULD NOT BE THE SOLE CRITERION FOR IDENTIFYING APOPTOSIS [J].
COLLINS, RJ ;
HARMON, BV ;
GOBE, GC ;
KERR, JFR .
INTERNATIONAL JOURNAL OF RADIATION BIOLOGY, 1992, 61 (04) :451-453