Hydrogen Peroxide Inducible DNA Cross-Linking Agents: Targeted Anticancer Prodrugs

被引:273
|
作者
Kuang, Yunyan [1 ,2 ]
Baakrishnan, Kumudha [3 ]
Gandhi, Varsha [3 ]
Peng, Xiaohua [1 ]
机构
[1] Univ Wisconsin, Dept Chem & Biochem, Milwaukee, WI 53211 USA
[2] Fudan Univ, Dept Chem, Shanghai 200433, Peoples R China
[3] Univ Texas MD Anderson Canc Ctr, Dept Expt Therapeut, Houston, TX 77030 USA
关键词
QUINONE METHIDES; LIVING CELLS; CANCER; DUPLEX; SUBSTITUENTS; NUCLEOTIDE; STRESS; REPAIR; PROBES; OXYGEN;
D O I
10.1021/ja2073824
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The major concern for anticancer chemotherapeutic agents is the host toxicity. The development of anticancer prodrugs targeting the unique biochemical alterations in cancer cells is an attractive approach to achieve therapeutic activity and selectivity. We designed and synthesized a new type of nitrogen mustard prodrug that can be activated by high level of reactive oxygen species (ROS) found in cancer cells to release the active chemotherapy agent. The activation mechanism was determined by NMR analysis. The activity and selectivity of these prodrugs toward ROS was determined by measuring DNA interstrand cross-links and/or DNA alkylations. These compounds showed 60-90% inhibition toward various cancer cells, while normal lymphocytes were not affected. To the best of our knowledge, this is the first example of H2O2-activated anticancer prodrugs.
引用
收藏
页码:19278 / 19281
页数:4
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