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肝癌中的河马样激酶-Yes 关联蛋白通路。

The hippo-yes association protein pathway in liver cancer.

机构信息

Department of Gastroenterology, Shanghai 10th People's Hospital, Tongji University, School of Medicine, No. 301, Yanchang Road, Shanghai 200072, China.

出版信息

Gastroenterol Res Pract. 2013;2013:187070. doi: 10.1155/2013/187070. Epub 2013 Aug 6.

Abstract

Hepatocellular carcinoma (HCC) is one of the most common malignancies worldwide and the third leading cause of cancer mortality. Despite continuing development of new therapies, prognosis for patients with HCC remains extremely poor. In recent years, control of organ size becomes a hot topic in HCC development. The Hippo signaling pathway has been delineated and shown to be critical in controlling organ size in both Drosophila and mammals. The Hippo kinase cascade, a singling pathway that antagonizes the transcriptional coactivator Yes-associated protein (YAP), plays an important role in animal organ size control by regulating cell proliferation and apoptosis rates. During HCC development, this pathway is likely inactivated in tumor initiated cells that escape suppressive constrain exerted by the surrounding normal tissue, thus allowing clonal expansion and tumor development. We have reviewed evolutionary changes in YAP as well as other components of the Hippo pathway and described the relationships between YAP genes and HCC. We also discuss regulation of transcription factors that are up- and downstream of YAP in liver cancer development.

摘要

肝细胞癌(HCC)是全球最常见的恶性肿瘤之一,也是癌症死亡的第三大主要原因。尽管新疗法不断发展,但 HCC 患者的预后仍然非常差。近年来,控制器官大小成为 HCC 发展的热门话题。Hippo 信号通路已经被阐明,并被证明在控制果蝇和哺乳动物的器官大小方面具有关键作用。Hippo 激酶级联反应是一条拮抗转录共激活因子 Yes 相关蛋白(YAP)的信号通路,通过调节细胞增殖和细胞凋亡率,在动物器官大小控制中发挥重要作用。在 HCC 发展过程中,该途径在肿瘤起始细胞中可能失活,这些肿瘤起始细胞逃避了周围正常组织施加的抑制性约束,从而允许克隆扩增和肿瘤发展。我们综述了 YAP 以及 Hippo 途径其他成分的进化变化,并描述了 YAP 基因与 HCC 之间的关系。我们还讨论了转录因子在肝癌发展中上下游的调节。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e3e/3748736/8e5a875bda63/GRP2013-187070.001.jpg

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