Antitumor activity and structure-activity relationship of heparanase inhibitors: Recent advances

被引:5
|
作者
Fu, Kaishuo [1 ]
Bai, Zhifeng [1 ]
Chen, Lanlan [1 ]
Ye, Wenchong [1 ]
Wang, Meizhu [1 ]
Hu, Jiliang [1 ]
Liu, Chunhui [2 ]
Zhou, Wen [1 ]
机构
[1] Guangzhou Univ Chinese Med, Univ Town, Sch Pharmaceut Sci, E 232,Waihuan Rd, Guangzhou 510006, Peoples R China
[2] Shandong Univ, Sch Pharmaceut Sci, Inst Biochem & Biotechnol Drugs, Key Lab Chem Biol,Minist Educ, Jinan 250012, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
Heparanase (HPSE); HPSE inhibitors; Antitumor activity; Structure-activity relationship (SAR); FIBROBLAST-GROWTH-FACTOR; TUMOR-GROWTH; TARGETING HEPARANASE; RADIATION-RESISTANCE; RONEPARSTAT SST0001; PANCREATIC-CANCER; ACID-DERIVATIVES; OVARIAN-CANCER; DNA-BINDING; IN-VITRO;
D O I
10.1016/j.ejmech.2020.112221
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Heparanase (HPSE)-directed tumor progression plays a crucial role in mediating tumor-host crosstalk and priming the tumor microenvironment, leading to tumor growth, metastasis and chemo-resistance. HPSE-mediated breakdown of structural heparan sulfate (HS) networks in the extracellular matrix (ECM) and basement membranes (BM) directly facilitates tumor growth and metastasis. Lysosome HPSE also induces multi-drug resistance via enhanced autophagy. Therefore, HPSE inhibitors development has become an attractive topic to block tumor growth and metastasis or eliminate drug resistance. In this review, we summarize HPSE inhibitors applied experimentally and clinically according to interaction with the binding sites of HPSE and participation of growth factors. The antitumor activity and structure-activity relationship (SAR) are also emphasized. (c) 2020 Elsevier Masson SAS. All rights reserved.
引用
收藏
页数:18
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