Riser Bruce L, Barnes Jeffrey L, Varani James
BLR Bio LLC, Kenosha, WI, USA.
The Department of Physiology and Biophysics, and Department of Medicine, Rosalind Franklin University of Medicine and Science, 3333 Green Bay Road, North Chicago, IL, USA.
J Cell Commun Signal. 2015 Dec;9(4):327-39. doi: 10.1007/s12079-015-0309-3. Epub 2015 Dec 23.
The CCN family of matricellular signaling proteins is emerging as a unique common link across multiple diseases and organs related to injury and repair. They are now being shown to play a central role in regulating the pathways to the initiation and resolution of normal wound healing and fibrosis in response to multiple forms of injury. Similarly, it is also emerging that they play a key role in regulating the establishment, growth, metastases and tissue regeneration in many forms of cancer via the interaction of cancer cells with the tumor stroma. Evidence has been recently provided that these proteins do not act independently but are co-regulated working in a yin/yang manner to alter the outcome of both normal physiological processes as well as pathology. The purpose of this review is to twofold. First, it will summarize work to date supporting CCN2 as a therapeutic target in the formation and progression of renal, skin, and other organ fibrosis, as well as cancer stroma formation. Second, it will highlight recent evidence for CCN3 as a counter-regulator and a potential therapeutic agent in these diseases with an exciting, novel potential to both treat and then restore tissue homeostasis in those afflicted by these devastating disorders.
CCN 家族的基质细胞信号蛋白正逐渐成为多种与损伤和修复相关的疾病及器官之间独特的共同纽带。现已表明,它们在调节多种形式损伤后正常伤口愈合和纤维化的起始与消退途径中发挥核心作用。同样,也逐渐发现它们通过癌细胞与肿瘤基质的相互作用,在多种癌症的发生、发展、转移及组织再生过程中起关键作用。最近有证据表明,这些蛋白质并非独立发挥作用,而是以阴阳协同的方式共同调节,从而改变正常生理过程及病理过程的结果。本综述旨在实现两个目标。其一,总结迄今支持 CCN2 作为肾、皮肤及其他器官纤维化形成与进展以及癌症基质形成的治疗靶点的研究工作。其二,强调 CCN3 作为这些疾病的反向调节因子和潜在治疗剂的最新证据,其具有令人兴奋的新潜力,既能治疗又能恢复受这些毁灭性疾病折磨者的组织内稳态。