Cancer and Developmental Cell Biology Division, Institute of Molecular and Cell Biology, Singapore, Republic of Singapore.
J Cell Physiol. 2011 Apr;226(4):928-39. doi: 10.1002/jcp.22435.
The Hippo pathway is an evolutionally conserved protein kinase cascade involved in regulating organ size in vivo and cell contact inhibition in vitro by governing cell proliferation and apoptosis. Deregulation of the Hippo pathway is linked to cancer development. Its first core kinase Warts was identified in Drosophila more than 15 years ago, but it gained much attention when other core components of the pathway were identified 8 years later. Major discoveries of the pathway were made during past several years. The core kinase components Hippo, Salvador, Warts, and Mats in the fly and Mst1/2, WW45, Lats1/2, and Mob1 in mammals phosphorylate and inactivate downstream transcriptional co-activators Yorkie in the fly, Yes-associated protein (YAP) and transcriptional co-activator with PDZ-binding motif (TAZ) in mammals, respectively. Phosphorylated Yorkie, YAP, and TAZ are sequestered in the cytoplasm by interaction with 14-3-3 proteins. Here we review recent progresses of this pathway by focusing on how these proteins communicate with each other and how loss of regulation results in cancers.
Hippo 通路是一个进化上保守的蛋白激酶级联反应,通过调节细胞增殖和凋亡来参与调控体内器官大小和体外细胞接触抑制。Hippo 通路的失调与癌症的发生发展有关。其第一个核心激酶 Warts 早在 15 年前就在果蝇中被发现,但 8 年后其他通路的核心成分被鉴定出来后,它才引起了广泛关注。在过去的几年中,该通路的核心激酶成分 Hippo、Salvador、Warts 和 Mats 在果蝇中,以及 Mst1/2、WW45、Lats1/2 和 Mob1 在哺乳动物中,分别磷酸化并失活下游转录共激活因子 Yorkie、Yes 相关蛋白 (YAP) 和含有 PDZ 结合基序的转录共激活因子 (TAZ)。磷酸化的 Yorkie、YAP 和 TAZ 通过与 14-3-3 蛋白的相互作用被隔离在细胞质中。本文通过重点介绍这些蛋白如何相互作用以及调控缺失如何导致癌症,综述了该通路的最新进展。