Walia Amit, Yang Jessica F, Huang Yu-Hui, Rosenblatt Mark I, Chang Jin-Hong, Azar Dimitri T
Department of Ophthalmology and Visual Sciences, Illinois Eye and Ear Infirmary, University of Illinois at Chicago, Chicago, IL, USA.
Department of Ophthalmology and Visual Sciences, Illinois Eye and Ear Infirmary, University of Illinois at Chicago, Chicago, IL, USA.
Biochim Biophys Acta. 2015 Dec;1850(12):2422-38. doi: 10.1016/j.bbagen.2015.09.007. Epub 2015 Sep 12.
Angiogenesis is the process of neovascularization from pre-existing vasculature and is involved in various physiological and pathological processes. Inhibitors of angiogenesis, administered either as individual drugs or in combination with other chemotherapy, have been shown to benefit patients with various cancers. Endostatin, a 20-kDa C-terminal fragment of type XVIII collagen, is one of the most potent inhibitors of angiogenesis.
We discuss the biology behind endostatin in the context of its endogenous production, the various receptors to which it binds, and the mechanisms by which it acts. We focus on its inhibitory role in angiogenesis, lymphangiogenesis, and cancer metastasis. We also present emerging clinical applications for endostatin and its potential as a therapeutic agent in the form a short peptide.
The delicate balance between pro- and anti-angiogenic factors can be modulated to result in physiological wound healing or pathological tumor metastasis. Research in the last decade has emphasized an emerging clinical potential for endostatin as a biomarker and as a therapeutic short peptide. Moreover, elevated or depressed endostatin levels in diseased states may help explain the pathophysiological mechanisms of the particular disease.
Endostatin was once sought after as the 'be all and end all' for cancer treatment; however, research throughout the last decade has made it apparent that endostatin's effects are complex and involve multiple mechanisms. A better understanding of newly discovered mechanisms and clinical applications still has the potential to lead to future advances in the use of endostatin in the clinic.
血管生成是指从已有的脉管系统形成新血管的过程,参与多种生理和病理过程。血管生成抑制剂,无论是单独使用还是与其他化疗药物联合使用,已被证明对患有各种癌症的患者有益。内皮抑素是 XVIII 型胶原蛋白的一种 20 kDa C 末端片段,是最有效的血管生成抑制剂之一。
我们在其内源产生、与之结合的各种受体以及其作用机制的背景下讨论内皮抑素背后的生物学特性。我们重点关注其在血管生成、淋巴管生成和癌症转移中的抑制作用。我们还介绍了内皮抑素的新兴临床应用及其作为短肽形式的治疗剂的潜力。
促血管生成因子和抗血管生成因子之间的微妙平衡可以被调节,从而导致生理性伤口愈合或病理性肿瘤转移。过去十年的研究强调了内皮抑素作为生物标志物和治疗性短肽的新兴临床潜力。此外,疾病状态下内皮抑素水平的升高或降低可能有助于解释特定疾病的病理生理机制。
内皮抑素曾被视为癌症治疗的“终极解决方案”;然而,过去十年的研究表明,内皮抑素的作用是复杂的,涉及多种机制。更好地理解新发现的机制和临床应用仍有可能在临床上推动内皮抑素使用的未来进展。