Chemical toolbox to interrogate Heparanase-1 activity

乙酰肝素酶 硫酸乙酰肝素 血管生成 细胞外基质 化学生物学 辛迪康1 细胞生物学 糖胺聚糖 生物 化学 生物化学 计算生物学 癌症研究 细胞
作者
Zachary M. Rabinowitz,Johnathan Somers,Zhishen Wang,Lina Cui
出处
期刊:Current Opinion in Chemical Biology [Elsevier]
卷期号:80: 102452-102452
标识
DOI:10.1016/j.cbpa.2024.102452
摘要

The development of a robust chemical toolbox to interrogate the activity of heparanase-1 (HPSE-1), an endo-β-d-glucuronidase and the only known enzyme that cleaves heparan sulfate (HS), has become critically important. The primary function of HPSE-1, cleaving HS side chains from heparan sulfate proteoglycans (HSPGs), regulates the integrity of the extracellular matrix (ECM) and the bioavailability of active, heparan sulfate-binding partners such as enzymes, growth factors, chemokines, and cytokines. HPSE-1 enzymatic activity is strictly regulated and has been found to play fundamental roles in pathophysiological processes. HPSE-1 is significantly overexpressed under various conditions including cancer, metastasis, angiogenesis, and inflammation, making HPSE-1 a promising therapeutic and diagnostic target. Chemical tools that can detect and image HPSE-1 activity in vitro and/or in vivo can help drive the discovery of novel and efficacious anti-HPSE-1 drugs, investigate the basic biology of HPSE-1, and help serve as a diagnostic tool in clinical applications. Here, we will give an overview of the common chemical tools to detect HPSE-1 activity and highlight the novel heparanase probes recently developed in our lab.
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