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PMID: 1917140 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Increased ether lipid cytotoxicity by reducing membrane cholesterol content.

International journal of cancer ·Vol. 49 ·No. 3 ·1991-09-30 ·Pages 409-13

Diomede L, Piovani B, Modest EJ, Noseda A, Salmona M

Abstract

Ether-linked glycerophospholipids (ether lipids, EL) are selectively toxic and anti-proliferative agents against cancer cells in vitro. The reason for such selectivity is not completely clear. Their mechanism of action is mediated through an interaction with the plasma membrane and the membrane lipid composition may modulate it. As a continuation of previous reports, we now present data showing that cholesterol concentration modulates EL toxicity in the K562, U937 and MOLT4 leukemic cell lines in vitro. Cells become sensitive to otherwise ineffective doses of EL when their cholesterol content is lowered. Cell cholesterol levels were reduced by exposure to an egg lipid mixture (neutral glycerides, phosphatidylcholine and phosphatidylethanolamine, AL721). The data contribute to an understanding of the EL mechanism of action on membranes and suggest that the cellular cholesterol concentration must be considered a major factor in modulating the cytotoxic effects of EL.

MeSH Terms
Cholesterol/analysis,metabolism Humans Leukemia/drug therapy,metabolism Membrane Fluidity/drug effects Membrane Lipids/analysis,metabolism Phospholipid Ethers/metabolism,pharmacology Phospholipids/analysis,metabolism Tumor Cells, Cultured/chemistry,drug effects
Chemicals
Membrane Lipids Phospholipid Ethers Phospholipids Cholesterol
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Diomede L
Istituto di Ricerche Farmacologiche, Mario Negri, Milan, Italy.
Piovani B
Modest E J
Noseda A
Salmona M
Article Info
Journal
International journal of cancer
Abbr.
Int J Cancer
ISSN
0020-7136
Published
1991-09-30
Pages
409-13
Language
English
Region
United States
NLM ID
0042124
Subset
IM
Grants
NCI NIH HHS · CA41314 · United States
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