Yee Karen Kar Lye, Soo Khee Chee, Bay Boon Huat, Olivo Malini
Department of Medical Sciences, National Cancer Centre Singapore, Singapore.
Photochem Photobiol. 2002 Dec;76(6):678-82. doi: 10.1562/0031-8655(2002)076<0678:acopia>2.0.co;2.
Protoporphyrin IX dimethyl ester (PME), a dimethyl esterification of protoporphyrin IX (PpIX), exhibits higher intracellular uptake into NPC/CNE2 cells, a poorly differentiated human nasopharyngeal carcinoma, than does PpIX. Phototoxicity studies reveal PME to be a more potent photosensitizer than is PpIX, at the early and late incubation time points. Correlating phototoxicity with subcellular localization indicates that PME is a more potent photosensitizer when its primary target of photodamage is mitochondria. Also, additional targeting of lysosome enhances phototoxicity.
原卟啉IX二甲酯(PME)是原卟啉IX(PpIX)的二甲酯化产物,与PpIX相比,它在人低分化鼻咽癌NPC/CNE2细胞中的细胞内摄取率更高。光毒性研究表明,在早期和晚期孵育时间点,PME都是比PpIX更强效的光敏剂。将光毒性与亚细胞定位相关联表明,当PME的主要光损伤靶点是线粒体时,它是一种更强效的光敏剂。此外,对溶酶体的额外靶向作用会增强光毒性。