COMPARATIVE ANTI-MITOTIC EFFECTS OF LITHIUM GAMMA-LINOLENATE, GAMMA-LINOLENIC ACID AND ARACHIDONIC-ACID, ON TRANSFORMED AND EMBRYONIC-CELLS

Citation
Jc. Seegers et al., COMPARATIVE ANTI-MITOTIC EFFECTS OF LITHIUM GAMMA-LINOLENATE, GAMMA-LINOLENIC ACID AND ARACHIDONIC-ACID, ON TRANSFORMED AND EMBRYONIC-CELLS, Prostaglandins, leukotrienes and essential fatty acids, 59(4), 1998, pp. 285-291
Citations number
12
Categorie Soggetti
Cell Biology",Biology,"Endocrynology & Metabolism
ISSN journal
09523278
Volume
59
Issue
4
Year of publication
1998
Pages
285 - 291
Database
ISI
SICI code
0952-3278(1998)59:4<285:CAEOLG>2.0.ZU;2-3
Abstract
The effects of gamma-linolenic acid (GLA), the lithium salt of gamma-l inolenic acid (LiGLA) and arachidonic acid (AA) were compared at doses of 50 mu g/ml for periods of 6 and 24 h on cell cycle progression and apoptosis induction in transformed and in normal cells. In WHCO3 (oes ophageal cancer) cells and on primary embryonic equine lung cells, we found LiGLA to be the most effective in apoptosis induction. After 24 h, 94% of the WHCO3 cancer cells and 44% of the primary embryonic equi ne lung cells exposed to LiGLA were apoptotic. The WHCO3 cancer cells were also very susceptible to the apoptosis-inducing effects of AA (56 %) and GLA (44%), whereas the embryonic equine lung cells were much le ss affected by these two fatty acids. After 6 h exposure to all three compounds, most of the cycling WHCO3 cancer cells were blocked in S-ph ase. After 24 h treatment, some of the S-phase cells exposed to AA and GLA were apparently able to move into the G2/M phase, the LiGLA expos ed cells were mostly apoptotic and no cycling cells were present. The primary embryonic equine lung cells were fairly resistant to the cytot oxic effects of GLA and AA, From our studies we conclude that, althoug h LiGLA was the most toxic to the cancer cells, it is apparently less selective, compared to AA and GLA, in the killing of cancer and normal cells. it would also appear that the lithium might have added to the cytotoxic effects of LiGLA. The mechanism needs to be clarified.