Takigawa Yutaka, Brown Anthony M C
Department of Cell & Developmental Biology, Weill Cornell Medical College, New York, NY10065, USA.
Curr Drug Targets. 2008 Nov;9(11):1013-24. doi: 10.2174/138945008786786127.
Hepatocellular carcinoma (HCC) is a major cause of cancer death worldwide. As in many other types of cancer, aberrant activation of the canonical Wnt/beta-catenin signaling pathway is an important contributor to tumorigenesis. In HCC this frequently occurs through mutations in the N-terminal region of beta-catenin that stabilize the protein and permit an elevated level of constitutive transcriptional activation by beta-catenin/TCF complexes. In this article we review the abundant evidence that Wnt/beta-catenin signaling contributes to liver carcinogenesis. We also discuss what is known about the roles of Wnt signaling in liver development, regeneration, and stem cell behavior, in an effort to understand the mechanisms by which activation of the canonical Wnt pathway promotes tumor formation in this organ. The Wnt/beta-catenin pathway presents itself as an attractive target for developing novel rational therapies for HCC, a disease for which few successful treatment strategies are currently available.
肝细胞癌(HCC)是全球癌症死亡的主要原因。与许多其他类型的癌症一样,经典Wnt/β-连环蛋白信号通路的异常激活是肿瘤发生的重要因素。在HCC中,这种情况经常通过β-连环蛋白N端区域的突变发生,这些突变使该蛋白稳定,并使β-连环蛋白/TCF复合物的组成型转录激活水平升高。在本文中,我们综述了大量证据表明Wnt/β-连环蛋白信号通路有助于肝癌发生。我们还讨论了关于Wnt信号在肝脏发育、再生和干细胞行为中的作用的已知情况,以努力理解经典Wnt通路激活促进该器官肿瘤形成的机制。Wnt/β-连环蛋白通路是开发针对HCC的新型合理疗法的有吸引力的靶点,目前针对这种疾病几乎没有成功的治疗策略。