Cytotoxic effects of ether lipids and derivatives in human nonneoplastic bone marrow cells and leukemic cells in vitro

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Abstract
The effects of 2‐lysophosphatidylcholine (2‐LPC), the alkyl lysophospholipid derivatives (ALP) 1‐O‐octadecyl‐2‐O‐methyl‐rac‐glycero‐3‐phosphocholine (ET‐18‐OCH3) and 1‐O‐hexadecyl‐sn‐glycero‐3‐phospho‐trimethyl‐ammonio‐hexanol, the 2‐acetamide analog of platelet‐activating factor (PAF) 1‐O‐octadecyl‐2‐acetamide‐sn‐glycero‐3‐phosphocholine, the thioether lysophospholipid derivative (TLP) BM 41.440 and the ether‐linked lipoidal amine CP‐46,665 on tritiated thymidine uptake and trypan blue dye exclusion were tested in vitro in various freshly explanted cell samples from human nonneoplastic bone marrow and human leukemias. In both assay systems, a dose range of 1–20 μg/ml of the compounds was tested after 24, 48 and 72 hr of coincubation with the cells.The trypan blue dye exclusion revealed statistically significant preferential cytotoxicity in leukemic cells for three compounds with the order of quantitative selectiveness: ET‐18‐OCH3>BM41.440>2‐acetamide analog of PAF. CP‐46,665 was the most toxic compound, but did not reveal significant differences between nonneoplastic bone marrow and leukemic cells when added in concentrations greater than 1 μg/ml. The trimethyl‐ammoniohexanol compound showed only minor activity in the majority of tests, when added at concentrations 50% of the controls). Based on these results, ET‐18‐OCH3 and BM 41.440 are recommended for experimental bone marrow purging.