Department of General Surgery, The Third Xiangya Hospital, Central South University, Changsha, Hunan, China.
Drug Deliv. 2021 Dec;28(1):2051-2061. doi: 10.1080/10717544.2021.1983071.
Fibrotic diseases pose significant clinical challenges due to their broadness and complexity. Thus, a better understanding of fibrogenesis and the development of more effective treatments is imperative. Recent evidence suggests a significant antifibrotic potential of an endogenous glycoprotein, endostatin. While endostatin has been widely studied for its role as an anticancer adjuvant by inhibiting tumor angiogenesis, its possible implication in fibrosis remains largely unclear. Here, we review the role of endostatin in various cellular processes and highlight its antifibrotic activity. We hypothesize that endostatin conveys a homeostatic function in the process of fibrosis by regulating (a) TGF-β1 and its downstream signaling; (b) RhoA/ROCK pathway; (c) NF-κB signaling pathway; (d) expression of EGR-1; (e) PDGF/PDGFR pathway; (f) autophagy-related pathways; (g) pathways associated with cell proliferation and apoptosis. Finally, we propose a schematic model of the antifibrotic roles and mechanisms of endostatin; also, we outline future research directions of endostatin and aim to present a potential therapeutic approach for fibrosis.
纤维化疾病由于其广泛性和复杂性,给临床带来了巨大的挑战。因此,更好地了解纤维化的发生机制和开发更有效的治疗方法是至关重要的。最近的证据表明,一种内源性糖蛋白——内皮抑素具有显著的抗纤维化潜力。虽然内皮抑素已被广泛研究作为一种抗癌辅助剂,通过抑制肿瘤血管生成来发挥作用,但它在纤维化中的潜在作用在很大程度上仍不清楚。在这里,我们回顾了内皮抑素在各种细胞过程中的作用,并强调了它的抗纤维化活性。我们假设内皮抑素通过调节(a)TGF-β1 及其下游信号通路;(b)RhoA/ROCK 通路;(c)NF-κB 信号通路;(d)EGR-1 的表达;(e)PDGF/PDGFR 通路;(f)自噬相关通路;(g)与细胞增殖和凋亡相关的通路,在纤维化过程中发挥着一种稳态功能。最后,我们提出了内皮抑素抗纤维化作用和机制的示意图模型;并概述了内皮抑素的未来研究方向,旨在为纤维化提供一种潜在的治疗方法。