Matrix metalloproteinase-activated doxorubicin prodrugs inhibit HT1080 xenograft growth better than doxorubicin with less toxicity.
第一作者:
Charles F,Albright
第一单位:
Bristol-Myers Squibb Pharmaceutical Research Institute, 5 Research Parkway, Wallingford, CT 06492, USA. Charlie.Albright@BMS.com
作者:
主题词
动物(Animals);多柔比星(Doxorubicin);药物筛选试验, 抗肿瘤(Drug Screening Assays, Antitumor);纤维肉瘤(Fibrosarcoma);人类(Humans);基质金属蛋白酶2(Matrix Metalloproteinase 2);基质金属蛋白酶9(Matrix Metalloproteinase 9);基质金属蛋白酶类, 膜相关(Matrix Metalloproteinases, Membrane-Associated);金属内肽酶类(Metalloendopeptidases);小鼠(Mice);脑啡肽酶(Neprilysin);肽碎片(Peptide Fragments);药物前体(Prodrugs);网状细胞(Reticulocytes);移植, 异种(Transplantation, Heterologous);肿瘤细胞, 培养的(Tumor Cells, Cultured)
DOI
10.1158/1535-7163.MCT-05-0006
PMID
15897239
发布时间
2020-09-30
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