Abstract |
Cleavage of heparan sulfate proteoglycans (HSPGs) by the enzyme heparanase modulates tumour-related events including angiogenesis, cell invasion, and metastasis. Metalloshielding of heparan sulfate (HS) by positively charged polynuclear platinum complexes (PPCs) effectively inhibits physiologically critical HS functions. Studies using bacterial P. heparinus heparinase II showed that a library of Pt complexes varying in charge and nuclearity and the presence or absence of a dangling amine inhibits the cleavage activity of the enzyme on the synthetic pentasaccharide, Fondaparinux (FPX). Charge-dependent affinity of PPC for FPX was seen in competition assays with methylene blue and ethidium bromide. The dissociation constant (Kd ) of TriplatinNC for FPX was directly measured by isothermal titration calorimetry (ITC). The trend in DFT calculated interaction energies with heparin fragments is consistent with the spectroscopic studies. Competitive inhibition of TAMRA-R9 internalization in human carcinoma (HCT116) cells along with studies in HCT116, wildtype CHO and mutant CHO-pgsA745 (lacking HS/CS) cells confirm that HSPG-mediated interactions play an important role in the cellular accumulation of PPCs.
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Authors | Anil Kumar Gorle, Samantha J Katner, Wyatt E Johnson, Daniel E Lee, A Gerard Daniel, Eric P Ginsburg, Mark von Itzstein, Susan J Berners-Price, Nicholas P Farrell |
Journal | Chemistry (Weinheim an der Bergstrasse, Germany)
(Chemistry)
Vol. 24
Issue 25
Pg. 6606-6616
(May 02 2018)
ISSN: 1521-3765 [Electronic] Germany |
PMID | 29655185
(Publication Type: Journal Article)
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Copyright | © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim. |
Chemical References |
- Heparan Sulfate Proteoglycans
- Oligosaccharides
- Organoplatinum Compounds
- Polysaccharides
- triplatinNC
- Heparin
- Heparitin Sulfate
- heparanase
- Glucuronidase
- Fondaparinux
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Topics |
- Animals
- Fondaparinux
- Glucuronidase
(metabolism)
- HCT116 Cells
- Heparan Sulfate Proteoglycans
(pharmacology)
- Heparin
(metabolism)
- Heparitin Sulfate
(pharmacology)
- Humans
- Nuclear Magnetic Resonance, Biomolecular
- Oligosaccharides
- Organoplatinum Compounds
(chemistry, pharmacology)
- Polysaccharides
(pharmacology)
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