نتایج جستجو برای: yap gene

تعداد نتایج: 1145607  

Journal: :iranian journal of radiation research 0
s.h. kim korea atomic energy research institute, jeongeup, 580-185, south korea j. k. kim korea atomic energy research institute, jeongeup, 580-185, south korea

background: all aerobically growing organisms suffer from exposure to oxidative stress, caused by partially reduced forms of molecular oxygen, known as reactive oxygen species (ros). these are highly reactive and capable of damaging cellular constituents such as dna, lipids and proteins. consequently, cells from many different organisms have evolved mechanisms to protect their components agains...

Journal: :Circulation research 2015
Zhiqiang Lin Pingzhu Zhou Alexander von Gise Fei Gu Qing Ma Jinghai Chen Haidong Guo Pim R R van Gorp Da-Zhi Wang William T Pu

RATIONALE Yes-associated protein (YAP), the nuclear effector of Hippo signaling, regulates cellular growth and survival in multiple organs, including the heart, by interacting with TEA (transcriptional enhancer activator)-domain sequence-specific DNA-binding proteins. Recent studies showed that YAP stimulates cardiomyocyte proliferation and survival. However, the direct transcriptional targets ...

Journal: :The EMBO journal 2004
Sayyed K Zaidi Andrew J Sullivan Ricardo Medina Yoshiaki Ito Andre J van Wijnen Janet L Stein Jane B Lian Gary S Stein

Src/Yes tyrosine kinase signaling contributes to the regulation of bone homeostasis and inhibits osteoblast activity. Here we show that the endogenous Yes-associated protein (YAP), a mediator of Src/Yes signaling, interacts with the native Runx2 protein, an osteoblast-related transcription factor, and suppresses Runx2 transcriptional activity in a dose-dependent manner. Runx2, through its PY mo...

Journal: :Genes & development 2008
Bin Zhao Xin Ye Jindan Yu Li Li Weiquan Li Siming Li Jianjun Yu Jiandie D Lin Cun-Yu Wang Arul M Chinnaiyan Zhi-Chun Lai Kun-Liang Guan

The YAP transcription coactivator has been implicated as an oncogene and is amplified in human cancers. Recent studies have established that YAP is phosphorylated and inhibited by the Hippo tumor suppressor pathway. Here we demonstrate that the TEAD family transcription factors are essential in mediating YAP-dependent gene expression. TEAD is also required for YAP-induced cell growth, oncogenic...

2017
Dan Xue Qiongying Wei Xiaoping Li Tingyan Lin

Lung cancer is a most common malignancy in both men and women. Studies have indicated that YAP gene was closely related to chemo-resistance of cancers. However, whether YAPS expression participates in the resistance of human lung cancer A549 cells to Taxol (TAX) remains unclear. The aim of this study is to investigate the role of YAP in the resistance of A549 cells to TAX. The sensitivity of ce...

2018
Madhura Kulkarni Tuan Zea Tan Nurfarhanah Bte Syed Sulaiman John M. Lamar Prashali Bansal Jianzhou Cui Yiting Qiao Yoshiaki Ito

Hippo pathway target, YAP has emerged as an important player in solid tumor progression. Here, we identify RUNX1 and RUNX3 as novel negative regulators of oncogenic function of YAP in the context of breast cancer. RUNX proteins are one of the first transcription factors identified to interact with YAP. RUNX1 or RUNX3 expression abrogates YAP-mediated pro-tumorigenic properties of mammary epithe...

2016
Kwong-Fai Wong Angela M. Liu Wanjin Hong Zhi Xu John M. Luk

The Hippo pathway regulates the down-stream target Yes-associated protein (YAP) to maintain organ homeostasis, which is commonly inactivated in many types of cancers. However, how cell adhesion dysregulates the Hippo pathway activating YAP oncogene in hepatocellular carcinoma (HCC) remains unclear. Our findings demonstrate that α2β1 integrin (but not other β1 integrins) expressed in HCC cells, ...

2016
Ping-Chih Hsu Bin You Yi-Lin Yang Wen-Qian Zhang Yu-Cheng Wang Zhidong Xu Yuyuan Dai Shu Liu Cheng-Ta Yang Hui Li Bin Hu David M. Jablons Liang You

Yes-associated protein (YAP) is a main mediator of the Hippo pathway, which promotes cancer development. Here we show that YAP promotes resistance to erlotinib in human non-small cell lung cancer (NSCLC) cells. We found that forced YAP overexpression through YAP plasmid transfection promotes erlotinib resistance in HCC827 (exon 19 deletion) cells. In YAP plasmid-transfected HCC827 cells, GTIIC ...

Journal: :Molecular cancer research : MCR 2015
Samantha E Hiemer Liye Zhang Vinay K Kartha Trevor S Packer Munirah Almershed Vikki Noonan Maria Kukuruzinska Manish V Bais Stefano Monti Xaralabos Varelas

UNLABELLED Oral squamous cell carcinoma (OSCC) is a prevalent form of cancer that develops from the epithelium of the oral cavity. OSCC is on the rise worldwide, and death rates associated with the disease are particularly high. Despite progress in understanding the mutational and expression landscape associated with OSCC, advances in deciphering these alterations for the development of therape...

Journal: :Circulation research 2014
Zhiqiang Lin Alexander von Gise Pingzhu Zhou Fei Gu Qing Ma Jianming Jiang Allan L Yau Jessica N Buck Katryna A Gouin Pim R R van Gorp Bin Zhou Jinghai Chen Jonathan G Seidman Da-Zhi Wang William T Pu

RATIONALE Yes-associated protein (YAP), the terminal effector of the Hippo signaling pathway, is crucial for regulating embryonic cardiomyocyte proliferation. OBJECTIVE We hypothesized that YAP activation after myocardial infarction (MI) would preserve cardiac function and improve survival. METHODS AND RESULTS We used a cardiac-specific, inducible expression system to activate YAP in adult ...

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