Department of Molecular Biology, Massachusetts General Hospital, Simches Research Building, 6408, 185 Cambridge Street, Boston, MA 02115, USA.
Br J Cancer. 2011 Jan 4;104(1):24-32. doi: 10.1038/sj.bjc.6606011. Epub 2010 Nov 23.
The mechanisms controlling mammalian organ size have long been a source of fascination for biologists. These controls are needed to both ensure the integrity of the body plan and to restrict inappropriate proliferation that could lead to cancer. Regulation of liver size is of particular interest inasmuch as this organ maintains the capacity for regeneration throughout life, and is able to regain precisely its original mass after partial surgical resection. Recent studies using genetically engineered mouse strains have shed new light on this problem; the Hippo signalling pathway, first elucidated as a regulator of organ size in Drosophila, has been identified as dominant determinant of liver growth. Defects in this pathway in mouse liver lead to sustained liver overgrowth and the eventual development of both major types of liver cancer, hepatocellular carcinoma and cholangiocarcinoma. In this review, we discuss the role of Hippo signalling in liver biology and the contribution of this pathway to liver cancer in humans.
长期以来,控制哺乳动物器官大小的机制一直是生物学家关注的焦点。这些控制机制不仅需要确保身体计划的完整性,还需要限制可能导致癌症的不当增殖。肝脏大小的调节特别令人感兴趣,因为肝脏在整个生命周期中都保持着再生能力,并且能够在部分外科切除后准确地恢复其原始质量。最近使用基因工程小鼠品系的研究为此问题提供了新的线索;Hippo 信号通路最初被阐明为果蝇中器官大小的调节剂,已被确定为肝脏生长的主要决定因素。该通路在小鼠肝脏中的缺陷导致持续的肝脏过度生长,并最终导致两种主要类型的肝癌,肝细胞癌和胆管细胞癌的发展。在这篇综述中,我们讨论了 Hippo 信号在肝脏生物学中的作用以及该途径对人类肝癌的贡献。