Letterio John J
Laboratary of Cell Regulation and Carcinogenesis, The Center for Cancer Research, NCI, NIH, Bethesda, MD 20892-5055, USA.
Mutat Res. 2005 Aug 25;576(1-2):120-31. doi: 10.1016/j.mrfmmm.2005.03.004.
There is considerable complexity underlying the mechanisms through which the TGF-beta signaling pathway regulates the initiation and progression of cancer. Analysis of this pathway and the role that it plays in human malignancy continues to elucidate novel mechanisms through which various genetic and epigenetic events subvert the controls that TGF-beta exerts over cell growth, differentiation, and malignant transformation. Modeling these events in the mouse represents an important goal, as the relevant preclinical models are essential not only for improving our understanding of the role of the TGF-beta pathway in the molecular pathogenesis of cancer, but also as tools for evaluating the impact of novel therapeutics on TGF-beta signaling and the role they may play in the prevention and treatment of malignancies. Here, we consider highlights from a number of in vivo murine model systems and relate a few of the significant observations to what we know about TGF-beta signaling in human cancer.
转化生长因子-β(TGF-β)信号通路调控癌症发生和发展的机制存在相当大的复杂性。对该信号通路及其在人类恶性肿瘤中所起作用的分析,不断揭示各种遗传和表观遗传事件颠覆TGF-β对细胞生长、分化和恶性转化控制的新机制。在小鼠中模拟这些事件是一个重要目标,因为相关的临床前模型不仅对于增进我们对TGF-β信号通路在癌症分子发病机制中作用的理解至关重要,而且作为评估新型疗法对TGF-β信号传导的影响以及它们在恶性肿瘤预防和治疗中可能发挥作用的工具也必不可少。在此,我们探讨了一些体内小鼠模型系统的要点,并将一些重要观察结果与我们对人类癌症中TGF-β信号传导的了解联系起来。