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6-O-endosulfatases in tumor metastasis: heparan sulfate proteoglycans modification and potential therapeutic targets.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
Am J Cancer Res. 2024 Feb 25;14(2):897-916. doi: 10.62347/RXVE7097. eCollection 2024.
2
SULFs in human neoplasia: implication as progression and prognosis factors.人类肿瘤中的 SULFs:作为进展和预后因素的意义。
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3
Organ-specific sulfation patterns of heparan sulfate generated by extracellular sulfatases Sulf1 and Sulf2 in mice.细胞外硫酸酯酶 Sulf1 和 Sulf2 在小鼠中产生的肝素硫酸的器官特异性硫酸化模式。
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The SULFs, extracellular sulfatases for heparan sulfate, promote the migration of corneal epithelial cells during wound repair.SULFs(硫酸乙酰肝素的细胞外硫酸酯酶)可促进角膜上皮细胞在创伤修复过程中的迁移。
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Front Neuroanat. 2021 Aug 20;15:726718. doi: 10.3389/fnana.2021.726718. eCollection 2021.
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Heparan sulfate 6-O-endosulfatases, Sulf1 and Sulf2, regulate glomerular integrity by modulating growth factor signaling.硫酸乙酰肝素6-O-内硫酸酯酶Sulf1和Sulf2通过调节生长因子信号传导来调节肾小球完整性。
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The Role of Heparanase and Sulfatases in the Modification of Heparan Sulfate Proteoglycans within the Tumor Microenvironment and Opportunities for Novel Cancer Therapeutics.肝素酶和硫酸酯酶在肿瘤微环境中修饰硫酸乙酰肝素蛋白聚糖中的作用及新型癌症治疗的机会。
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Sulfatase 2 Modulates Fate Change from Motor Neurons to Oligodendrocyte Precursor Cells through Coordinated Regulation of Shh Signaling with Sulfatase 1.硫酸酯酶2通过与硫酸酯酶1协同调节Shh信号通路来调控运动神经元向少突胶质前体细胞的命运转变。
Dev Neurosci. 2017;39(5):361-374. doi: 10.1159/000464284. Epub 2017 May 11.

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Biomedicines. 2025 Jun 14;13(6):1471. doi: 10.3390/biomedicines13061471.
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Decoding glycosylation in cardiovascular diseases: mechanisms, biomarkers, and therapeutic opportunities.解析心血管疾病中的糖基化:机制、生物标志物及治疗机遇
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3
Heparan-6-O-endosulfatase 2, a cancer-related proteoglycan enzyme, is effectively inhibited by a specific sea cucumber fucosylated glycosaminoglycan.硫酸乙酰肝素-6-O-内切硫酸酯酶2,一种与癌症相关的蛋白聚糖酶,被一种特定的海参岩藻糖基化糖胺聚糖有效抑制。
Glycobiology. 2025 Apr 23;35(6). doi: 10.1093/glycob/cwaf025.

本文引用的文献

1
Involvement of the kynurenine pathway in breast cancer: updates on clinical research and trials.犬尿氨酸途径在乳腺癌中的作用:临床研究和试验的最新进展。
Br J Cancer. 2023 Aug;129(2):185-203. doi: 10.1038/s41416-023-02245-7. Epub 2023 Apr 11.
2
Cancer-Associated Fibroblast: Role in Prostate Cancer Progression to Metastatic Disease and Therapeutic Resistance.癌相关成纤维细胞:在前列腺癌向转移性疾病和治疗抵抗进展中的作用。
Cells. 2023 Mar 4;12(5):802. doi: 10.3390/cells12050802.
3
Tumor microenvironment-mediated immune evasion in hepatocellular carcinoma.肿瘤微环境介导的肝细胞癌免疫逃逸。
Front Immunol. 2023 Feb 10;14:1133308. doi: 10.3389/fimmu.2023.1133308. eCollection 2023.
4
Metastatic colorectal cancer: mechanisms and emerging therapeutics.转移性结直肠癌:机制与新兴治疗策略。
Trends Pharmacol Sci. 2023 Apr;44(4):222-236. doi: 10.1016/j.tips.2023.01.003. Epub 2023 Feb 23.
5
Spatially resolved transcriptomics revealed local invasion-related genes in colorectal cancer.空间分辨转录组学揭示了结直肠癌中与局部侵袭相关的基因。
Front Oncol. 2023 Feb 1;13:1089090. doi: 10.3389/fonc.2023.1089090. eCollection 2023.
6
RNA epigenetic modifications in ovarian cancer: The changes, chances, and challenges.卵巢癌中的RNA表观遗传修饰:变化、机遇与挑战。
Wiley Interdiscip Rev RNA. 2023 Sep-Oct;14(5):e1784. doi: 10.1002/wrna.1784. Epub 2023 Feb 21.
7
Lung cancer immunotherapy: progress, pitfalls, and promises.肺癌免疫疗法:进展、陷阱和前景。
Mol Cancer. 2023 Feb 21;22(1):40. doi: 10.1186/s12943-023-01740-y.
8
Glioblastoma and Other Primary Brain Malignancies in Adults: A Review.成人脑胶质瘤和其他原发性脑恶性肿瘤:综述。
JAMA. 2023 Feb 21;329(7):574-587. doi: 10.1001/jama.2023.0023.
9
Heterogeneity and plasticity of epithelial-mesenchymal transition (EMT) in cancer metastasis: Focusing on partial EMT and regulatory mechanisms.肿瘤转移中上皮-间质转化(EMT)的异质性和可塑性:关注部分 EMT 和调控机制。
Cell Prolif. 2023 Jun;56(6):e13423. doi: 10.1111/cpr.13423. Epub 2023 Feb 19.
10
Unraveling the function of epithelial-mesenchymal transition (EMT) in colorectal cancer: Metastasis, therapy response, and revisiting molecular pathways.解析上皮-间质转化(EMT)在结直肠癌中的作用:转移、治疗反应及重新审视分子途径
Biomed Pharmacother. 2023 Apr;160:114395. doi: 10.1016/j.biopha.2023.114395. Epub 2023 Feb 15.

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.

DOI:10.62347/RXVE7097
PMID:38455409
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10915330/
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。