نتایج جستجو برای: mst1

تعداد نتایج: 453  

Journal: :Cancer research 2016
Xiaoying Zhang Cai Guo Xiwei Wu Arthur X Li Limin Liu Walter Tsark Reinhard Dammann Hui Shen Steven L Vonderfecht Gerd P Pfeifer

The tumor suppressor gene RASSF1A is epigenetically silenced in most human cancers. As a binding partner of the kinases MST1 and MST2, the mammalian orthologs of the Drosophila Hippo kinase, RASSF1A is a potential regulator of the Hippo tumor suppressor pathway. RASSF1A shares these properties with the scaffold protein SAV1. The role of this pathway in human cancer has remained enigmatic inasmu...

2011
Pei Wang Yujie Bai Bangrong Song Yadong Wang Dong Liu Yongqiang Lai Xiaolin Bi Zengqiang Yuan

BACKGROUND The Hippo/MST1 signaling pathway plays an important role in the regulation of cell proliferation and apoptosis. As a major downstream target of the Hippo/MST1 pathway, YAP2 (Yes-associated protein 2) functions as a transcriptional cofactor that has been implicated in many biological processes, including organ size control and cancer development. MST1/Lats kinase inhibits YAP2's nucle...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2007
Eunha Hwang Kyoung-Seok Ryu Kimmo Pääkkönen Peter Güntert Hae-Kap Cheong Dae-Sik Lim Jie-Oh Lee Young Ho Jeon Chaejoon Cheong

In eukaryotic cells, apoptosis and cell cycle arrest by the Ras --> RASSF --> MST pathway are controlled by the interaction of SARAH (for Salvador/Rassf/Hippo) domains in the C-terminal part of tumor suppressor proteins. The Mst1 SARAH domain interacts with its homologous domain of Rassf1 and Rassf5 (also known as Nore1) by forming a heterodimer that mediates the apoptosis process. Here, we des...

2012
Claudia Dittfeld Antje M. Richter Katrin Steinmann Antje Klagge-Ulonska Reinhard H. Dammann

The Ras association domain family 1A (RASSF1A) tumor suppressor encodes a Sav-RASSF-Hpo domain (SARAH), which is an interaction domain characterized by hWW45 (dSAV) and MST1/2 (dHpo). In our study, the interaction between RASSF1A and RASSF1C with MST1 and MST2 was demonstrated and it was shown that this interaction depends on the SARAH domain. SARAH domain-deleted RASSF1A had a similar growth-r...

2014
Amin Ardestani Federico Paroni Zahra Azizi Supreet Kaur Vrushali Khobragade Ting Yuan Thomas Frogne Wufan Tao Jose Oberholzer Francois Pattou Julie Kerr Conte Kathrin Maedler

nature medicine VOLUME 20 | NUMBER 4 | APRIL 2014 385 Pancreatic beta cell death is the fundamental cause of type 1 diabetes (T1D) and a contributing factor to the reduced beta cell mass in type 2 diabetes (T2D)1–4. In both cases, the mechanisms of beta cell death are complex and as yet not fully defined. Thus, multiple triggering factors have been identified; these factors initiate a variety o...

Journal: :Oncology reports 2014
Xu-Hui Zhou Chao-Qun Yang Cheng-Lin Zhang Yang Gao Hong-Bin Yuan Ce Wang

Ras association (RalGDS/AF-6) domain family member RASSF5 has been implicated in a variety of key biological processes, including cell proliferation, cell cycle regulation and apoptosis. It is believed to play an important role in tumorigenesis as a tumor suppressor in a number of malignancies. Yet, little is known concerning the function and underlying mechanisms of RASSF5 in human osteosarcom...

Journal: :Journal of the American Society of Nephrology 2020

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