Growth inhibitory effects of liposome-associated 1-O-octadecyl-2-O-methyl-sn-glycero-3-phosphocholine
Autor: | Imran Ahmad, Andrew C. Peters, Andrew S. Janoff, Marina Y. Pushkareva, Eric Mayhew |
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Rok vydání: | 1997 |
Předmět: |
Cell division
DNA Fragmentation Biology Hemolysis Biochemistry Mice chemistry.chemical_compound Neoplasms Tumor Cells Cultured Animals Humans Phosphocholine Liposome Organic Chemistry Phospholipid Ethers Cell Biology Molecular biology chemistry Drug Resistance Neoplasm Cell culture Apoptosis Liposomes DNA fragmentation Calcium Growth inhibition Cell Division Intracellular |
Zdroj: | Lipids. 32:1045-1054 |
ISSN: | 1558-9307 0024-4201 |
DOI: | 10.1007/s11745-997-0135-8 |
Popis: | The growth inhibitory effects of 1-O-octadecyl-2-O-methyl-sn-glycero-3-phosphocholine (ET-18-OCH3) and various liposome compositions of ET-18-OCH3 were compared in a standardized growth inhibition assay utilizing a diverse tumor cell line panel including cell lines expressing multidrug resistance. ET-18-OCH3 and ELL-12 (4:3:1:2, dioleoylphosphatidylcholine/ cholesterol/dioleoylphosphatidylethanolamine-glutaric acid/ET-18-OCH3), an optimal liposomal ET-18-OCH3 formulation, inhibited growth in the micromolar range in drug-sensitive and -resistant cells. In general, ET-18-OCH3-liposomes were about twofold less growth inhibitory than ET-18-OCH3. However, the known hemolytic effects of ET-18-OCH3 were greatly reduced, up to 20 or more times, by liposome association. The effects of ET-18-OCH3 and ELL-12 were compared in intracellular [Ca2+] modulation and DNA fragmentation assays. ET-18-OCH3 elicited both concentration- and serum-dependent transient and permanent increases in intracellular [Ca2+]. In contrast, ELL-12 did not modulate intracellular [Ca2+]. ET-18-OCH3 and ELL-12 similarly affected DNA fragmentation, which may be indicative of apoptosis. The results suggest that, although the specific growth inhibitory effects of ET-18-OCH3 and ELL-12 are similar, associating ET-18-OCH3 with stable well-characterized liposomes eliminates nonspecific cell membrane-associated lytic effects. |
Databáze: | OpenAIRE |
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