Sudhakar Akulapalli, Boosani Chandra S
Cell Signaling and Tumor Angiogenesis Laboratory, Department of Genetics, Boys Town National Research Hospital, Omaha, NE 68132, USA.
Gene Regul Syst Bio. 2007 Oct 14;1:217-26. doi: 10.4137/grsb.s345.
Vascular basement membrane (VBM) derived molecules are regulators of certain biological activities such as cell growth, differentiation and angiogenesis. Angiogenesis is regulated by a systematic controlled balance between VBM derived antiangiogenic factors and proangiogenic growth factors. In the normal physiological state, equilibrium is maintained between the antiangiogenic and proangiogenic factors. The antiangiogenic factors (molecules), which are generated by the proteolytic cleavage of the VBM, include; alpha1 chain non-collagenous (NC1) domain of type XVIII collagen (endostatin) and the NC1 domains from the alpha chains of Type IV collagen considered as endogenous angiogenesis inhibitors. These collagen derived NC1 domains have a pivotal role in the regulation of tumor angiogenesis, thus making them attractive alternate candidates for cancer therapies. In this review we illustrate a comprehensive overview of the knowledge gained from the signaling mechanisms of Type IV collagen derived endogenous inhibitors in angiogenesis.
血管基底膜(VBM)衍生分子是某些生物活性的调节因子,如细胞生长、分化和血管生成。血管生成受VBM衍生的抗血管生成因子和促血管生成生长因子之间系统控制的平衡调节。在正常生理状态下,抗血管生成和促血管生成因子之间保持平衡。由VBM蛋白水解裂解产生的抗血管生成因子(分子)包括: XVIII型胶原的α1链非胶原(NC1)结构域(内皮抑素)和IV型胶原α链的NC1结构域,它们被视为内源性血管生成抑制剂。这些胶原衍生的NC1结构域在肿瘤血管生成的调节中起关键作用,因此使其成为癌症治疗有吸引力的替代候选物。在这篇综述中,我们全面概述了从IV型胶原衍生的内源性抑制剂在血管生成中的信号传导机制中获得的知识。