Comparison of hexadecylphosphocholine with fish oil as an antitumor agent

Daniel T. Colombo, Lisa K. Tran, Jamie J. Speck, Ronald C. Reitz
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引用次数: 4

Abstract

Hexadecylphosphocholine (HePC) reduced the growth of the human mammary tumor, MX-1, in the athymic nude mouse similar to the fish oil, MaxEPA. When used together, HePC and MaxEPA were additive towards reducing tumor growth. An unsaturated alkylphosphocholine mixture, ShisoPC, was not as effective as HePC in reducing tumor growth. MaxEPA reduced tumor PGE2 levels greater than 90%, while HePC and the ShisoPC only reduced tumor PGE2 40–60% with HePC being slightly better than ShisoPC. MaxEPA markedly increased the cellular ω3 fatty acids and decreased 20:4ω6, the substrate for PGE2. HePC did not alter the tumor fatty acid composition, but it significantly lowered the total fatty acid concentration of the tumor by about 47%. In addition, phosphatidylcholine and sphingomyelin decreased in tumors from animals treated with HePC, and alterations in other phospholipids also were noted. These data suggest that different mechanisms exist for HePC and fish oil in reducing tumor growth.

十六烷基磷脂胆碱与鱼油抗肿瘤作用的比较
Hexadecylphosphocholine (HePC)与鱼油MaxEPA类似,在胸腺裸鼠中抑制人乳腺肿瘤MX-1的生长。当HePC和MaxEPA一起使用时,它们具有抑制肿瘤生长的作用。不饱和烷基磷胆碱混合物(ShisoPC)在抑制肿瘤生长方面不如HePC有效。MaxEPA对肿瘤PGE2的抑制作用大于90%,而HePC和ShisoPC对肿瘤PGE2的抑制作用仅为40 ~ 60%,HePC略优于ShisoPC。MaxEPA显著增加细胞中ω3脂肪酸,降低PGE2底物20:4ω6脂肪酸。HePC不改变肿瘤脂肪酸组成,但显著降低肿瘤总脂肪酸浓度约47%。此外,用HePC治疗动物的肿瘤中磷脂酰胆碱和鞘磷脂减少,其他磷脂也发生了变化。这些数据表明HePC和鱼油在抑制肿瘤生长方面存在不同的机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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