Photosensitization of pancreatic tumour cells by delta-aminolaevulinic acid esters.

Anti-cancer drug design Pub Date : 2000-06-01
C J Whitaker, S H Battah, M J Forsyth, C Edwards, R W Boyle, E K Matthews
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Abstract

A series of straight chain, branched and cyclo-delta-aminolaevulinic acid (ALA) esters have been synthesized and their photosensitizing properties analysed using an in vitro system of rat pancreatoma cells. Structurally favourable ALA esters not only induced the formation of more of the endogenous photosensitizer, protoporphyrin IX (PpIX), but they did so at a faster rate than ALA itself. This action was reflected in a substantial increase in photocytotoxicity of some 270 times, using the more potent ALA esters. An important structural feature was identified in two of the ALA esters which greatly limited PpIX production, i.e. a branch point located next to the site of ester cleavage. Experiments on the transport of ALA and of ALA esters across the cell membrane showed that ALA, but not ALA esters, gain access to the cell via the di- and tripeptide transporter, PEPTI. Finally, these results show that the esterification of ALA can greatly increase its cellular uptake, so generating more intracellular PpIX, improved tumour cell photosensitization and enhanced photocytotoxicity.

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氨基乙酰丙酸酯对胰腺肿瘤细胞的光敏作用。
本文合成了一系列直链、支链和环-三角洲氨基乙酰丙酸酯,并在体外大鼠胰脏瘤细胞系统中分析了它们的光敏特性。结构有利的ALA酯不仅诱导更多内源性光敏剂原卟啉IX (PpIX)的形成,而且其形成速度比ALA本身更快。这种作用反映在使用更有效的ALA酯后,光细胞毒性增加了约270倍。在两种ALA酯中发现了一个重要的结构特征,即位于酯裂解位点附近的分支点,这极大地限制了PpIX的产生。ALA和ALA酯在细胞膜上的转运实验表明,ALA,而不是ALA酯,通过二肽和三肽转运体PEPTI进入细胞。最后,这些结果表明ALA的酯化可以大大增加其细胞摄取,从而在细胞内产生更多的PpIX,改善肿瘤细胞的光敏性,增强光细胞毒性。
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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