Superior therapeutic efficacy of N-l-leucyl-doxorubicin versus doxorubicin in human melanoma xenografts correlates with higher tumour concentrations of free drug
- 1 July 1999
- journal article
- Published by Elsevier in European Journal Of Cancer
- Vol. 35 (7) , 1143-1149
- https://doi.org/10.1016/s0959-8049(99)00074-x
Abstract
No abstract availableKeywords
This publication has 25 references indexed in Scilit:
- The antitumour activity of the prodrug N-l-leucyl-doxorubicin and its parent compound doxorubicin in human tumour xenograftsEuropean Journal Of Cancer, 1998
- Different Roles for Plasminogen Activators and Metalloproteinases in Melanoma MetastasisPublished by Springer Nature ,1996
- Clinical relevance of cathepsin B-like enzyme activity and cysteine proteinase inhibitor in melanocytic tumoursArchives of Dermatological Research, 1995
- The anti-tumour effects of the prodrugs N-l-leucyl-doxorubicin and vinblastine-isoleucinate in human ovarian cancer xenograftsBritish Journal of Cancer, 1992
- A possible role for cysteine proteinase and its inhibitors in motility of malignant melanoma and other tumour cellsMelanoma Research, 1992
- Cathepsin B: association with plasma membrane in metastatic tumors.Proceedings of the National Academy of Sciences, 1986
- Accumulation and metabolism of new anthracycline derivatives in the heart after IV injection into miceCancer Chemotherapy and Pharmacology, 1982
- A covalent linkage between daunorubicin and proteins that is stable in serum and reversible by lysosomal hydrolases, as required for a lysosomotropic drug-carrier conjugate: in vitro and in vivo studies.Proceedings of the National Academy of Sciences, 1982
- Amino acid and dipeptide derivatives of daunorubicin. 1. Synthesis, physicochemical properties, and lysosomal digestionJournal of Medicinal Chemistry, 1980
- Amino acid and dipeptide derivatives of daunorubicin. 2. Cellular pharmacology and antitumor activity of L1210 leukemic cells in vitro and in vivoJournal of Medicinal Chemistry, 1980