Effects of photoactivated 5-aminolevulinic acid hexyl ester on MDR1 over-expressing human uterine sarcoma cells

被引:24
作者
Chu, Ellie S. M. [1 ]
Yow, Christine M. N. [1 ]
Shi, Mark [2 ]
Ho, Rodney J. Y. [2 ]
机构
[1] Hong Kong Polytech Univ, Med Lab Sci Sect, Dept Hlth Technol & Informat, Hong Kong, Hong Kong, Peoples R China
[2] Univ Washington, Dept Pharmaceut, Seattle, WA 98195 USA
关键词
5-Aminolevulinic acid hexyl ester; Photodynamic therapy; Multi-drug resistance; MDR1; P-glycoprotein;
D O I
10.1016/j.toxlet.2008.06.860
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 [卫生毒理学];
摘要
The role of multi-drug resistance (MDR1) and its product, P-glycoprotein (P-gp) on 5-aminolevulinic acid hexyl ester (Hexyl-ALA) mediated phototoxicity was determined with human uterine sarcoma cells, MES-SA control and MDR1 expressing MES-SA-Dx5. MDR1 expression reduced intracellular levels of the Hexyl-ALA metabolite, protoporphyrin IX (PpIX) to a limited degree and could be reversed with a P-gp inhibitor, verapamil. P-gp expression also reduced Hexyl-ALA photosensitivity. More importantly, photoactivated Hexyl-ALA reduced at the mRNA and protein levels without altering housekeeping GAPDH mRNA. These findings suggest that Hexyl-ALA could be used to selectively reduce P-gp expression in overcoming resistance to chemotherapy agents such as doxorubicin and paclitaxel. (C) 2008 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:7 / 12
页数:6
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