Biochemistry Department, Universidade Federal de São Paulo (UNIFESP), São Paulo, SP, Brazil.
Adv Exp Med Biol. 2020;1221:821-845. doi: 10.1007/978-3-030-34521-1_36.
In this chapter, we will emphasize the importance of heparan sulfate proteoglycans (HSPG) in controlling various physiological and pathological molecular mechanisms and discuss how the heparanase enzyme can modulate the effects triggered by HSPG. Additionally, we will also navigate about the existing knowledge of the possible role of heparanase-2 in biological events. Heparan sulfate is widely distributed and evolutionarily conserved, evidencing its vital importance in cell development and functions such as cell proliferation, migration, adhesion, differentiation, and angiogenesis. During remodeling of the extracellular matrix, the breakdown of heparan sulfate by heparanase results in the release of molecules containing anchored glycosaminoglycan chains of great interest in heparanase-mediated cell signaling pathways in various physiological states, tumor development, inflammation, and other diseases. Taken together, it appears that heparanase plays a key role in the maintenance of the pathology of cancer and inflammatory diseases and is a potential target for anti-cancer therapies. Therefore, heparanase inhibitors are currently being examined in clinical trials as novel cancer therapeutics. Heparanase-2 has no enzymatic activity, displays higher affinity for heparan sulfate and the coding region alignment shows 40% identity with the heparanase gene. Heparanase-2 plays an important role in embryogenic development however its mode of action and biological function remain to be elucidated. Heparanase-2 functions as an inhibitor of the heparanase-1 enzyme and also inhibits neovascularization mediated by VEGF. The HPSE2 gene is repressed by the Polycomb complex, together suggesting a role as a tumor suppressor.
在这一章中,我们将强调硫酸乙酰肝素蛋白聚糖(HSPG)在控制各种生理和病理分子机制方面的重要性,并讨论肝素酶酶如何调节 HSPG 引发的作用。此外,我们还将探讨肝素酶-2 在生物事件中可能发挥的作用的现有知识。硫酸乙酰肝素广泛分布且在进化上保守,这表明它在细胞发育和功能中至关重要,例如细胞增殖、迁移、黏附、分化和血管生成。在细胞外基质重塑过程中,肝素酶对硫酸乙酰肝素的分解导致释放含有锚定糖胺聚糖链的分子,这些分子在各种生理状态、肿瘤发展、炎症和其他疾病的肝素酶介导的细胞信号通路中具有重要意义。综上所述,肝素酶似乎在癌症和炎症性疾病的病理维持中发挥关键作用,是癌症治疗的潜在靶点。因此,肝素酶抑制剂目前正在临床试验中作为新型癌症治疗药物进行研究。肝素酶-2 没有酶活性,对硫酸乙酰肝素具有更高的亲和力,并且编码区比对显示与肝素酶基因有 40%的同源性。肝素酶-2 在胚胎发生发育中发挥重要作用,但其作用方式和生物学功能仍有待阐明。肝素酶-2 作为肝素酶-1 酶的抑制剂发挥作用,还可以抑制 VEGF 介导的新血管生成。HPSE2 基因受 Polycomb 复合物抑制,共同提示其作为肿瘤抑制因子的作用。