The PG500 series: novel heparan sulfate mimetics as potent angiogenesis and heparanase inhibitors for cancer therapy

• Published in: Investigational new drugs Vol. 28; no. 3; pp. 276 - 283
• Main Authors: Dredge, K., Hammond, E., Davis, K., Li, C. P., Liu, L., Johnstone, K., Handley, P., Wimmer, N., Gonda, T. J., Gautam, A., Ferro, V., Bytheway, I.
• Format: Journal Article
• Language: English
• Published: Boston Springer US 01.06.2010; Springer Nature B.V
• Subjects: Angiogenesis; Anticoagulants; Anticoagulants - pharmacology; Anticoagulants - therapeutic use; Antineoplastic Agents - pharmacology; Antineoplastic Agents - therapeutic use; Binding sites; Cancer therapies; Cell culture; Cell growth; Cell Line; Cell Line, Tumor; Cell Proliferation - drug effects; Chemical compounds; Drug Discovery - methods; Drug Evaluation, Preclinical - methods; Extracellular matrix; Fibroblast Growth Factor 1 - metabolism; Fibroblast Growth Factor 2 - metabolism; Fibroblasts; Glucuronidase - antagonists & inhibitors; Heparan sulfate; Heparitin Sulfate - analogs & derivatives; Heparitin Sulfate - pharmacology; Heparitin Sulfate - therapeutic use; Humans; Inhibitor drugs; Laboratories; Liver cancer; Medical research; Medicine; Medicine & Public Health; Metastasis; Neoplasms - drug therapy; Neovascularization, Pathologic - drug therapy; Oncology; Penicillin; Pharmaceuticals; Pharmacology; Pharmacology/Toxicology; Preclinical Studies; Software; Structure-Activity Relationship; Tumors; Vascular endothelial growth factor; Vascular Endothelial Growth Factor A - metabolism; Heparan sulfate; Heparanase; Angiogenesis; Cancer therapy
• ISSN: 0167-6997; 1573-0646
• DOI: 10.1007/s10637-009-9245-5

Summary Heparan sulfate mimetics, which we have called the PG500 series, have been developed to target the inhibition of both angiogenesis and heparanase activity. This series extends the technology underpinning PI-88, a mixture of highly sulfated oligosaccharides which reached Phase III clinical development for hepatocellular carcinoma. Advances in the chemistry of the PG500 series provide numerous advantages over PI-88. These new compounds are fully sulfated, single entity oligosaccharides attached to a lipophilic moiety, which have been optimized for drug development. The rational design of these compounds has led to vast improvements in potency compared to PI-88, based on in vitro angiogenesis assays and in vivo tumor models. Based on these and other data, PG545 has been selected as the lead clinical candidate for oncology and is currently undergoing formal preclinical development as a novel treatment for advanced cancer.