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

机译:CTGF是组织重塑和纤维化的主要介质其抑制作用可以逆转纤维化过程

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摘要

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.
机译:CTGF是一种分泌的基质细胞蛋白,具有非常复杂的生物学特性。已经显示出它可以调节许多信号传导途径,从而导致细胞粘附和迁移,血管生成,成肌纤维细胞活化以及细胞外基质沉积和重塑,这些共同导致组织重塑和纤维化。已有文献报道,当观察到大量胶原蛋白沉积后,siRNA抑制CTGF表达可防止CCl4诱导的肝纤维化,并可逆转纤维化。目前正在临床开发中的针对CTGF的单克隆抗体(FG-3019)已显示出在糖尿病合并症大鼠模型中逆转血管僵硬和改善心脏功能的能力。 FG-3019在鼠辐射诱发的肺纤维化模型中也表现出活性。当通过CT成像观察到FG-3019对小鼠给药后,放射线诱导的肺密度显着增加后,观察到肺密度在抗体施用期间降低,并在治疗后保持稳定停止了。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。

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