scholarly journals Interaction of S100A1 with LATS1 promotes cell growth through regulation of the Hippo pathway in hepatocellular carcinoma

Author(s):  
Qingping Guo ◽  
Jiale Wang ◽  
Zeyu Cao ◽  
Yongchang Tang ◽  
Chao Feng ◽  
...  
2018 ◽  
Vol 10 (3) ◽  
pp. 267-269
Author(s):  
Xueyan Ma ◽  
Peixue Li ◽  
Peihao Chen ◽  
Jinhui Li ◽  
Hongling Huang ◽  
...  

2017 ◽  
Vol 400 ◽  
pp. 175-182 ◽  
Author(s):  
Xuan Shi ◽  
Hai-Rong Zhu ◽  
Tao-Tao Liu ◽  
Xi-Zhong Shen ◽  
Ji-Min Zhu

2020 ◽  
Vol 26 (4) ◽  
pp. 742-750
Author(s):  
Yuchen Liu ◽  
Xiaohui Wang ◽  
Yingzi Yang

Primary liver cancer is one of the most common cancer worldwide. Hepatocellular carcinoma (HCC) in particular, is the second leading cause of cancer deaths in the world. The Hippo signaling pathway has emerged as a major oncosuppressive pathway that plays critical roles inhibiting hepatocyte proliferation, survival, and HCC formation. A key component of the Hippo pathway is the inhibition of yes-associated protein (YAP)/transcriptional co-activator with PDZ-binding motif (TAZ) transcription factors by the Hippo kinase cascade. Aberrant activation of YAP or TAZ has been found in several human cancers including HCC. It is also well established that YAP/TAZ activation in hepatocytes causes HCC in mouse models, indicating that YAP/TAZ are potential therapeutic targets for human liver cancer. In this review, we summarize the recent findings regarding the multifarious roles of Hippo/YAP/TAZ in HCC development, and focus on their cell autonomous roles in controlling hepatocyte proliferation, differentiation, survival and metabolism as well as their non-cell autonomous in shaping the tumor microenvironment.


2013 ◽  
Vol 11 (7) ◽  
pp. 748-758 ◽  
Author(s):  
Ei Yong Ahn ◽  
Ji Su Kim ◽  
Gi Jeong Kim ◽  
Young Nyun Park

2021 ◽  
Author(s):  
Debatrayee Sinha ◽  
Denisa Ivan ◽  
Ellie Gibbs ◽  
Madhurya Chetluru ◽  
John W Goss ◽  
...  

Polycystins are evolutionally conserved cation channels. Mutations of human polycystins lead to one of the most common genetic disorders, Autosomal Dominant Polycystic Kidney Disorder. Interestingly, the fission yeast homologue Pkd2p is required for cytokinesis the last stage of cell division, but the mechanism remains unclear. Motivated by our discovery of the epistatic genetic interactions between pkd2 and the Hippo pathway Septation Initiation Network (SIN), we investigated their interplay during cytokinesis. We found that pkd2 modulated the localization as well as the activities of SIN. Most notably, pkd2 promotes a transition to cell size growth during cytokinesis, opposed by SIN. The role of Pkd2p in cell growth is not limited to cytokinesis. A newly isolated pkd2 temperature-sensitive mutant largely blocked the tip expansion of cells during interphase. Such growth defect was accompanied by frequent shrinking, reduced cell volume, and decreased cell stiffness. We conclude that Pkd2p promotes transition to the post-mitosis cell growth in coordination with the Hippo pathway


2016 ◽  
Vol 80 (7) ◽  
pp. 1511-1519 ◽  
Author(s):  
Shohei Ikeda ◽  
Junichi Sadoshima

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