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肿瘤转移中的6-O-硫酸酯酶:硫酸乙酰肝素蛋白聚糖修饰及潜在治疗靶点

6-O-endosulfatases in tumor metastasis: heparan sulfate proteoglycans modification and potential therapeutic targets.

作者信息

Han Mengzhen, Zhu He, Chen Xiaoping, Luo Xin

机构信息

Hepatic Surgery Center, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology Wuhan 430030, Hubei, China.

Hubei Key Laboratory of Hepato-Pancreato-Biliary Diseases Wuhan 430030, Hubei, China.

出版信息

Am J Cancer Res. 2024 Feb 25;14(2):897-916. doi: 10.62347/RXVE7097. eCollection 2024.

Abstract

Metastasis is the leading cause of cancer-associated mortality. Although advances in the targeted treatment and immunotherapy have improved the management of some cancers, the prognosis of metastatic cancers remains unsatisfied. Therefore, the specific mechanisms in tumor metastasis need further investigation. 6-O-endosulfatases (SULFs), comprising sulfatase1 (SULF1) and sulfatase 2 (SULF2), play pivotal roles in the post-synthetic modifications of heparan sulfate proteoglycans (HSPGs). Consequently, these extracellular enzymes can regulate a variety of downstream pathways by modulating HSPGs function. During the past decades, researchers have detected the expression of SULF1 and SULF2 in most cancers and revealed their roles in tumor progression and metastasis. Herein we reviewed the metastasis steps which SULFs participated in, elucidated the specific roles and mechanisms of SULFs in metastasis process, and discussed the effects of SULFs in different types of cancers. Moreover, we summarized the role of targeting SULFs in combination therapy to treat metastatic cancers, which provided some novel strategies for cancer therapy.

摘要

转移是癌症相关死亡的主要原因。尽管靶向治疗和免疫疗法的进展改善了某些癌症的治疗,但转移性癌症的预后仍不尽人意。因此,肿瘤转移的具体机制需要进一步研究。6-O-硫酸酯酶(SULFs),包括硫酸酯酶1(SULF1)和硫酸酯酶2(SULF2),在硫酸乙酰肝素蛋白聚糖(HSPGs)的合成后修饰中起关键作用。因此,这些细胞外酶可以通过调节HSPGs功能来调节多种下游途径。在过去几十年中,研究人员在大多数癌症中检测到SULF1和SULF2的表达,并揭示了它们在肿瘤进展和转移中的作用。在此,我们回顾了SULFs参与的转移步骤,阐明了SULFs在转移过程中的具体作用和机制,并讨论了SULFs在不同类型癌症中的作用。此外,我们总结了靶向SULFs在联合治疗转移性癌症中的作用,为癌症治疗提供了一些新策略。

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