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CCN2: a bona fide target for anti-fibrotic drug intervention

机译:CCN2:抗纤维化药物干预的真正靶标

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摘要

CCN2 (formerly known as connective tissue growth factor) was identified by several different laboratories approximately 20 years ago. Almost since its identification as a factor induced in normal fibroblasts by transforming growth factor β and overexpressed in fibrotic disease, CCN2 has been hypothesized to be not only a marker but also a central mediator of fibrosis in vivo. Finally, in vivo data are emerging to validate this key hypothesis. For example, a neutralizing anti-CCN2 antibody was found to attenuate fibrogenesis in three separate animal models (Wang et al. in Fibrogenesis Tissue Repair 4:1–4, ). This commentary addresses recent data indicating that CCN2 appears to represent a key central mediator of fibrosis and a good target for anti-fibrotic drug intervention.
机译:大约20年前,几个不同的实验室鉴定出CCN2(以前称为结缔组织生长因子)。自从将CCN2鉴定为通过转化生长因子β在正常成纤维细胞中诱导并在纤维化疾病中过度表达的因子以来,它就被认为不仅是体内纤维化的标志物,而且是纤维化的主要介质。最后,体内数据正在出现,以验证这一关键假设。例如,在三种不同的动物模型中,发现一种中和性抗CCN2抗体可减弱纤维发生(Wang等人,《纤维发生组织修复》 4:1-4)。这篇评论评论了最近的数据,这些数据表明CCN2似乎代表了纤维化的关键中心介质,并且是抗纤维化药物干预的良好靶标。

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