Hypoxia-Targeting Organometallic Ru(II)-Arene Complexes with Enhanced Anticancer Activity in Hypoxic Cancer Cells

被引:39
作者
Zhao, Jian [1 ,2 ,3 ]
Li, Wanchun [1 ,2 ]
Gou, Shaohua [1 ,2 ,3 ]
Li, Shuang [1 ,2 ]
Lin, Shengqiu [1 ,2 ]
Wei, Qianhui [1 ,2 ]
Xu, Gang [1 ,2 ,3 ]
机构
[1] Southeast Univ, Pharmaceut Res Ctr, Nanjing 211189, Jiangsu, Peoples R China
[2] Southeast Univ, Sch Chem & Chem Engn, Nanjing 211189, Jiangsu, Peoples R China
[3] Southeast Univ, Jiangsu Prov Hitech Key Lab Biomed Res, Nanjing 211189, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
RUTHENIUM(II) ARENE COMPLEXES; ANTITUMOR-ACTIVITY; IN-VITRO; HEPATOCELLULAR-CARCINOMA; CLINICAL DEVELOPMENT; PT(IV) PRODRUGS; PLATINUM DRUGS; AGENT; INHIBITION; THERAPY;
D O I
10.1021/acs.inorgchem.8b01070
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
As hypoxia is an important factor to limit chemotherapeutic efficacy in tumors, we herein report three ruthenium(II) arene complexes containing a hypoxia inducible factor-la inhibitor (YC-1), which endow the organometallic complexes with potential for hypoxia targeting. In vitro tests showed the resulting complexes had higher anticancer activities in hypoxia than in normoxia against the tested cancer cell lines. Western blot analysis revealed that complexes 1-3 blocked HIF-1 alpha protein accumulation under hypoxic conditions. Moreover, these complexes displayed much less cytotoxicity toward the normal human umbilical vein endothelial cell line (HUVEC), indicating that complexes 1-3 may be selectively cytotoxic for human cancer cell lines. These findings proved that ligation with YC-1 endowed these organometallic ruthenium(II) complexes with potential for hypoxia targeting in addition to enhancing their anticancer activities.
引用
收藏
页码:8396 / 8403
页数:8
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