Targeting heparanase in cancer: inhibition by synthetic, chemically modified, and natural compounds

CD Mohan, S Hari, HD Preetham, S Rangappa… - Iscience, 2019 - cell.com
Heparanase is an endoglycosidase involved in remodeling the extracellular matrix and
thereby in regulating multiple cellular processes and biological activities. It cleaves heparan …

PI-88 and novel heparan sulfate mimetics inhibit angiogenesis

V Ferro, K Dredge, L Liu, E Hammond… - … in thrombosis and …, 2007 - thieme-connect.com
The heparan sulfate (HS) mimetic PI-88 is a promising inhibitor of tumor growth and
metastasis expected to commence phase III clinical evaluation in 2007 as an adjuvant …

Heparan sulfate mimetics in cancer therapy: the challenge to define structural determinants and the relevance of targets for optimal activity

C Lanzi, G Cassinelli - Molecules, 2018 - mdpi.com
Beyond anticoagulation, the therapeutic potential of heparin derivatives and heparan sulfate
(HS) mimetics (functionally defined HS mimetics) in oncology is related to their ability to bind …

Engineered sulfated polysaccharides for biomedical applications

Ø Arlov, D Rütsche, M Asadi Korayem… - Advanced Functional …, 2021 - Wiley Online Library
Sulfated polysaccharides are ubiquitous in living systems and have central roles in
biological functions such as organism development, cell proliferation and differentiation …

PI-88 and Related Heparan Sulfate Mimetic s

M Chhabra, V Ferro - Heparanase: From basic research to clinical …, 2020 - Springer
The heparan sulfate mimetic PI-88 (muparfostat) is a complex mixture of sulfated
oligosaccharides that was identified in the late 1990s as a potent inhibitor of heparanase. In …

A phase I biological and pharmacologic study of the heparanase inhibitor PI-88 in patients with advanced solid tumors

M Basche, DL Gustafson, SN Holden, CL O'Bryant… - Clinical Cancer …, 2006 - AACR
Purpose: PI-88 is a mixture of highly sulfated oligosaccharides that inhibits heparanase, an
extracellular matrix endoglycosidase, and the binding of angiogenic growth factors to …

Probing the interactions of phosphosulfomannans with angiogenic growth factors by surface plasmon resonance

S Cochran, C Li, JK Fairweather, WC Kett… - Journal of medicinal …, 2003 - ACS Publications
The binding interactions of the phosphosulfomannan anticancer agent PI-88 (1) with the
angiogenic growth factors FGF-1, FGF-2, and VEGF were studied by surface plasmon …

A synthetic heparanase inhibitor reduces proteinuria in passive Heymann nephritis

V Levidiotis, C Freeman, M Punler… - Journal of the …, 2004 - journals.lww.com
The β-D-endoglycosidase heparanase has been proposed to be important in the
pathogenesis of proteinuria by acting to selectively degrade the negatively charged side …

Targeting heparan sulfate proteoglycans and their modifying enzymes to enhance anticancer chemotherapy efficacy and overcome drug resistance

C Lanzi, N Zaffaroni, G Cassinelli - Current medicinal chemistry, 2017 - ingentaconnect.com
Targeting heparan sulfate proteoglycans (HSPGs) and enzymes involved in heparan sulfate
(HS) chain editing is emerging as a new anticancer strategy. The involvement of HSPGs in …

Synthesis, biological activity, and preliminary pharmacokinetic evaluation of analogues of a phosphosulfomannan angiogenesis inhibitor (PI-88)

T Karoli, L Liu, JK Fairweather… - Journal of medicinal …, 2005 - ACS Publications
The phosphosulfomannan 1 (PI-88) is a mixture of highly sulfated oligosaccharides that is
currently undergoing clinical evaluation in cancer patients. As well as its anticancer …