Disciplina de Biologia Molecular, Departamento de Bioquímica, Universidade Federal de São Paulo , São Paulo, SP, Brazil.
Instituto de Ciências Ambientais, Químicas e Farmacêuticas, Universidade Federal de São Paulo , Diadema, SP, Brazil.
Cancer Biol Ther. 2020 Dec 1;21(12):1087-1094. doi: 10.1080/15384047.2020.1838034. Epub 2020 Nov 12.
Heparan sulfate proteoglycans (HSPGs) play important roles in cancer initiation and progression, by interacting with the signaling pathways that affect proliferation, adhesion, invasion and angiogenesis. These roles suggest the possibility of various strategies of regulation of these molecules. In this review, we demonstrated that the anticancer drugs can regulate the heparan sulfate proteoglycans activity in different ways: some act directly in core protein, and can bind to a specific type of HSPG. Others drugs interact with glycosaminoglycans chains, and others can act directly in enzymes that regulate HSPGs levels. We also demonstrated that the HSPGs drug targets can be divided into four groups: monoclonal antibodies, antitumor antibiotic, natural products, and mimetics peptide. Interestingly, many drugs demonstrated in this review are approved by FDA and is used in cancer therapy (Food and Drug Administration) like trastuzumab, panitumumab, bleomycin and bisphosphonate zoledronic acid (ASCO) or are in clinical trials like codrituzumab and genistein. This review should help researchers to understand the mechanism of action of anticancer drugs existing and also may inspire the discovery of new drugs that regulate the heparan sulfate proteoglycans activity.
硫酸乙酰肝素蛋白聚糖(HSPGs)通过与影响增殖、黏附、侵袭和血管生成的信号通路相互作用,在癌症的发生和发展中发挥重要作用。这些作用表明了调节这些分子的各种策略的可能性。在这篇综述中,我们证明了抗癌药物可以通过不同的方式调节硫酸乙酰肝素蛋白聚糖的活性:一些药物直接作用于核心蛋白,并能与特定类型的 HSPG 结合。其他药物与糖胺聚糖链相互作用,还有一些可以直接作用于调节 HSPGs 水平的酶。我们还证明,HSPGs 的药物靶点可以分为四类:单克隆抗体、抗肿瘤抗生素、天然产物和模拟肽。有趣的是,许多在这篇综述中证明有效的药物已被 FDA 批准用于癌症治疗(美国食品和药物管理局),如曲妥珠单抗、帕尼单抗、博来霉素和双膦酸盐唑来膦酸(ASCO),或正在临床试验中,如 codrituzumab 和染料木黄酮。这篇综述应该有助于研究人员了解现有的抗癌药物的作用机制,也可能启发人们发现新的调节硫酸乙酰肝素蛋白聚糖活性的药物。