Yeger Herman, Perbal Bernard
Program in Developmental and Stem Cell Biology Research Institute, SickKids, Toronto, Canada.
International CCN Society, Marseille, France.
J Cell Commun Signal. 2021 Dec;15(4):491-517. doi: 10.1007/s12079-021-00618-2. Epub 2021 Apr 20.
Since the authors first reviewed this subject in 2016 significant progress has been documented in the CCN field with advances made in the understanding of how members of the CCN family of proteins, CCN1-6, contribute to the pathogenesis and progression, positive and negative, of a larger variety of cancers. As termed matricellular proteins, and more recently the connective communication network, it has become clearer that members of the CCN family interact complexly with other proteins in the extracellular microenvironment, membrane signaling proteins, and can also operate intracellularly at the transcriptional level. In this review we expand on this earlier information providing new detailed information and insights that appropriate a much greater involvement and importance of their role in multiple aspects of cancer. Despite all the new information many more questions have been raised and intriguing results generated that warrant greater investigation. In order to permit the reader to smoothly integrate the new information we discuss all relevant CCN members in the context of cancer subtypes. We have harmonized the nomenclature with CCN numbering for easier comparisons. Finally, we summarize what new has been learned and provide a perspective on how our knowledge about CCN1-6 is being used to drive new initiatives on cancer therapeutics.
自作者于2016年首次回顾该主题以来,CCN领域已取得显著进展,在理解CCN蛋白家族成员(CCN1 - 6)如何促进多种癌症的发病机制和进展(包括正向和负向)方面取得了进展。作为基质细胞蛋白,以及最近的结缔组织通讯网络,越来越清楚的是,CCN家族成员与细胞外微环境中的其他蛋白、膜信号蛋白复杂地相互作用,并且还可以在转录水平上在细胞内发挥作用。在本综述中,我们扩展了这一早期信息,提供了新的详细信息和见解,表明它们在癌症的多个方面发挥着更大的作用,具有更高的参与度和重要性。尽管有所有这些新信息,但更多问题被提出,并且产生了引人入胜的结果,值得进一步研究。为了使读者能够顺利整合新信息,我们在癌症亚型的背景下讨论所有相关的CCN成员。我们统一了命名法与CCN编号,以便于比较。最后,我们总结了所学到的新内容,并就我们对CCN1 - 6的了解如何用于推动癌症治疗的新举措提供了一个观点。