4-Hydroxyl-oxoisoaporphine, one small molecule as theranostic agent for simultaneous fluorescence imaging and photodynamic therapy as type II photosensitizer

被引:2
作者
Xu, Qi [1 ]
Ji, Yunfan [1 ]
Chen, Meijun [1 ]
Shao, Xusheng [1 ,2 ]
机构
[1] East China Univ Sci & Technol, Shanghai Key Lab Chem Biol, Sch Pharm, Shanghai 200237, Peoples R China
[2] East China Univ Sci & Technol, State Key Lab Bioreactor Engn, Shanghai 200237, Peoples R China
基金
中国国家自然科学基金;
关键词
Oxoisoaporphine; Photosensitizer; Cell imaging; Singlet oxygen; Cytotoxicity; BETA-AMYLOID AGGREGATION; TUMOR-CELL APOPTOSIS; G-QUADRUPLEX DNA; TELOMERASE ACTIVITY; SINGLET OXYGEN; OXOISOAPORPHINE; PHENALENONE; DERIVATIVES; COMPLEXES; ALKALOIDS;
D O I
10.1007/s43630-021-00030-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Oxoisoaporphine (OA) is a plant phototoxin isolated from Menispermaceae, however, its weak fluorescence and low water solubility impede it for theranostics. We developed here 4-hydroxyl-oxoisoaporphine (OHOA), which has good singlet oxygen-generating ability (0.06), strong fluorescence (0.72) and improved water solubility. OHOA displays excellent fluorescence for cell imaging and exhibits light-induced cytotoxicity against cancer cell. In vitro model of human cervical carcinoma (HeLa) cell proved that singlet oxygen generated by OHOA triggered photosensitized oxidation reactions and exert toxic effect on tumor cells. The MTT assay using HeLa cells verified the low cytotoxicity of OHOA in the dark and high phototoxicity. Confocal experiment indicates that OHOA mainly distributes in mitochondria and western blotting demonstrated that OHOA induces cell apoptosis via the mitochondrial pathway in the presence of light. Our molecule provides an alternative choice as a theranostic agent against cancer cells which usually are in conflict with each other for most traditional theranostic agents.
引用
收藏
页码:501 / 512
页数:12
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