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

机译:乙酰肝素酶抑制剂的抗肿瘤活性和结构 - 活性关系:最近的进展

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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.
机译:乙酰肝素酶(HPSE) - 分配的肿瘤进展在介导肿瘤 - 宿主串扰和引发肿瘤微环境中起着至关重要的作用,导致肿瘤生长,转移和化学抗性。 HPSE介导的细胞外基质(ECM)和基底膜(BM)中结构硫酸乙酰肝素硫酸盐(HS)网络的分解直接促进肿瘤生长和转移。 溶酶体HPSE还通过增强的自噬诱导多药物耐药性。 因此,HPSE抑制剂发育已成为阻断肿瘤生长和转移或消除耐药性的有吸引力的话题。 在本综述中,我们总结了在实验和临床上根据与HPSE的结合位点的相互作用进行了实验和临床应用的HPSE抑制剂。 还强调了抗肿瘤活动和结构 - 活动关系(SAR)。 (c)2020 Elsevier Masson SAS。 版权所有。

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