SGI-110 DNA Methyltransferase Inhibitor Oncolytic

被引:57
作者
Griffiths, E. A. [1 ]
Choy, G.
Redkar, S.
Taverna, P.
Azab, M.
Karpf, A. R.
机构
[1] Roswell Pk Canc Inst, Elm & Carlton Sts, Buffalo, NY 14263 USA
关键词
Hypomethylating prodrug; Myelodysplastic syndrome; Acute myeloid leukemia; Ovarian cancer; Hepatocellular carcinoma; SGI-110; MYELODYSPLASTIC SYNDROME; CYTOSINE-ARABINOSIDE; METHYLATION; 5-AZA-2'-DEOXYCYTIDINE; 5-AZACYTIDINE; DECITABINE; 5-AZA-2-DEOXYCYTIDINE; CANCER; GENE; PHARMACOKINETICS;
D O I
10.1358/dof.2013.38.8.1980499
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
SGI-110 is a second-generation hypomethylating prodrug whose active metabolite is the well-characterized drug decitabine. This novel compound is an oligonucleotide consisting of decitabine linked through a phosphodiester bond to the endogenous nucleoside deoxyguanosine. The dinucleotide configuration provides protection from drug clearance by deamination, while maintaining at least equivalent effects on gene-specific and global hypomethylation both in vitro and in animal model systems. This agent is currently being tested in phase I and II clinical trials in humans and has been demonstrated to be safe and well tolerated as a single agent, with evidence of promising activity in heavily pretreated (including currently FDA approved hypomethylating drugs) myelodysplastic syndrome and acute myeloid leukemia patients. Ongoing trials are also open in platinum-resistant ovarian cancer and hepatocellular carcinoma.
引用
收藏
页码:535 / 543
页数:9
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