CTGF is a central mediator of tissue remodeling and fibrosis and its inhibition can reverse the process of fibrosis.

Fibrogenesis & Tissue Repair Pub Date : 2012-06-06 eCollection Date: 2012-01-01 DOI:10.1186/1755-1536-5-S1-S24
Kenneth E Lipson, Carol Wong, Yuchin Teng, Suzanne Spong
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引用次数: 442

Abstract

CTGF is a secreted matricellular protein with very complex biology. It has been shown to modulate many signaling pathways leading to cell adhesion and migration, angiogenesis, myofibroblast activation, and extracellular matrix deposition and remodeling, which together lead to tissue remodeling and fibrosis. It has been reported in the literature that inhibition of CTGF expression by siRNA prevents CCl4-induced liver fibrosis and can reverse fibrosis when administered after significant collagen deposition is observed. A monoclonal antibody to CTGF that is currently in clinical development (FG-3019) has demonstrated the ability to reverse vascular stiffening and improve cardiac function in a rat model of diabetic complications. FG-3019 has also exhibited activity in a murine radiation-induced pulmonary fibrosis model. When FG-3019 was administered to mice after a significant radiation-induced increase in lung density could be observed by CT imaging, the density of the lungs was observed to decrease over the period during which the antibody was administered and to remain stable after therapy had ceased. When considered together, these data indicate that inhibition of CTGF can prevent and reverse the process of fibrosis.

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CTGF是组织重塑和纤维化的中心介质,其抑制可以逆转纤维化过程。
CTGF是一种分泌性基质细胞蛋白,具有非常复杂的生物学特性。它已被证明可以调节许多信号通路,导致细胞粘附和迁移、血管生成、肌成纤维细胞活化和细胞外基质沉积和重塑,这些共同导致组织重塑和纤维化。文献报道,通过siRNA抑制CTGF表达可预防ccl4诱导的肝纤维化,并在观察到明显的胶原沉积后给药可逆转纤维化。一种目前处于临床开发阶段的CTGF单克隆抗体(FG-3019)在糖尿病并发症大鼠模型中显示出逆转血管硬化和改善心功能的能力。FG-3019在小鼠辐射诱导的肺纤维化模型中也显示出活性。通过CT成像可以观察到放射引起的肺密度显著增加后,将FG-3019给予小鼠,观察到肺密度在给予抗体期间下降,并在治疗停止后保持稳定。综合考虑,这些数据表明抑制CTGF可以预防和逆转纤维化过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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