Abstract |
To improve the biological profile of 20(S)-camptothecin, a novel class of 20-O-linked camptothecin glycoconjugates has been designed for preferential cellular uptake into tumor cells by an active transport mechanism. Such conjugates have been optimized for enhanced solubility, stabilization of the camptothecin lactone ring, sufficient hydrolytic and proteolytic stability, and for an overall improvement in tumor selectivity. The constitution of the peptide spacer has a major impact on stability and biological activity of the conjugates both in vitro and in vivo. Glycoconjugates 17-22 with valine residues at the linkage position to camptothecin are sufficiently stable and show good antitumor activity in vitro against HT29 and other tumor cell lines. Fluorescence microscopy and flow cytometry experiments indicate that glycoconjugates such as 19 are taken up into lysosomal compartments of the tumor cell line HT29 by an active transport mechanism. The steric configuration of the particular amino acid residues linked to the camptothecin moiety has a major impact on the in vivo activity of the corresponding glycoconjugates in the breast cancer xenograft MX-1 model. Inhibiting tumor growth by >96%, the glycoconjugates 19 and 21 show the best activity in this particular model and have been investigated more extensively. The glycoconjugate 19 compares favorably to topotecan 4 and glycoconjugate 21 with respect to toxicity against hematopoietic stem cells and hepatocytes. Based on its profile, 19 has been selected for clinical trials.
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Authors | H G Lerchen, J Baumgarten, K von dem Bruch, T E Lehmann, M Sperzel, G Kempka, H H Fiebig |
Journal | Journal of medicinal chemistry
(J Med Chem)
Vol. 44
Issue 24
Pg. 4186-95
(Nov 22 2001)
ISSN: 0022-2623 [Print] United States |
PMID | 11708920
(Publication Type: Journal Article)
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Chemical References |
- 20-O-(Nalpha-(4-(3-O-methylfucopyranosyloxy)phenylaminothiocarbonyl)histidylvalyl)camptothecin
- Antineoplastic Agents
- Dipeptides
- Glycoconjugates
- Camptothecin
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Topics |
- Animals
- Antineoplastic Agents
(chemical synthesis, chemistry, pharmacology)
- Breast Neoplasms
(drug therapy)
- Camptothecin
(analogs & derivatives, chemical synthesis, chemistry, pharmacology)
- Cells, Cultured
- Dipeptides
(chemical synthesis, chemistry, pharmacology)
- Dogs
- Drug Design
- Drug Screening Assays, Antitumor
- Female
- Flow Cytometry
- Glycoconjugates
(chemical synthesis, chemistry, pharmacology)
- Hematopoiesis
(drug effects)
- Hepatocytes
(drug effects, enzymology)
- Humans
- Mice
- Mice, Inbred C57BL
- Microscopy, Confocal
- Microscopy, Fluorescence
- Rats
- Solubility
- Structure-Activity Relationship
- Transplantation, Heterologous
- Tumor Cells, Cultured
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