نتایج جستجو برای: c jnk

تعداد نتایج: 1062871  

Journal: :Cancer research 2000
L Xiao W Lang

Oncogenic (activated) Ras is a signal transducer that activates multiple effector-mediated signaling pathways leading to altered cell morphology, growth and differentiation, and neoplastic transformation. Activating mutations of Ras family genes have been detected in many types of human cancers, including lung cancer. However, the signaling mechanisms by which oncogenic Ras controls cancer cell...

2011
Ksenya Cohen-Katsenelson Tanya Wasserman Samer Khateb Alan J. Whitmarsh Ami Aronheim

JNK (c-Jun N-terminal kinase) is part of a MAPK (mitogen-activated protein kinase) signalling cascade. Scaffold proteins simultaneously associate with various components of the MAPK signalling pathway and play a crucial role in signal transmission and MAPK regulation. WDR62 (WD repeat domain 62) is a JNK scaffold protein. Recessive mutations within WDR62 result in severe cerebral cortical malfo...

Journal: :Molecular and cellular biology 2000
V L Gabai J A Yaglom V Volloch A B Meriin T Force M Koutroumanis B Massie D D Mosser M Y Sherman

Pretreatment with mild heat shock is known to protect cells from severe stress (acquired thermotolerance). Here we addressed the mechanism of this phenomenon by using primary human fibroblasts. Severe heat shock (45 degrees C, 75 min) of the fibroblasts caused cell death displaying morphological characteristics of apoptosis; however, it was caspase independent. This cell death process was accom...

Journal: :Cell 2005
Hideaki Kamata Shi-ichi Honda Shin Maeda Lufen Chang Hajime Hirata Michael Karin

TNFalpha is a pleiotropic cytokine that induces either cell proliferation or cell death. Inhibition of NF-kappaB activation increases susceptibility to TNFalpha-induced death, concurrent with sustained JNK activation, an important contributor to the death response. Sustained JNK activation in NF-kappaB-deficient cells was suggested to depend on reactive oxygen species (ROS), but how ROS affect ...

Journal: :Cancer research 1999
D Chauhan T Hideshima S Treon G Teoh N Raje S Yoshihimito Y T Tai W Li J Fan J DeCaprio K C Anderson

Previous studies have demonstrated that gamma-irradiation (IR)-induced apoptosis in multiple myeloma (MM) is associated with activation of stress-activated protein kinase (SAPK). In the present study, we examined the molecules downstream of SAPK/C-Jun N-terminal kinase (JNK), focusing on the role of retinoblastoma protein (Rb) during IR-induced MM cell apoptosis. The results demonstrate that IR...

2017
Yeting Hu Qian Xiao Haiyan Chen Jinjie He Yinuo Tan Yue Liu Zhanhuai Wang Qi Yang Xiangfeng Shen Yu Huang Ying Yuan Kefeng Ding

BEX2 has been suggested to promote the tumor growth in breast cancer and glioblastoma, while inhibit the proliferation of glioma cells. Thus, the role of BEX2 in tumor was still in debate. Additionally, the biological functions of BEX2 in colorectal cancer (CRC) have not yet been clarified. Here, we reported that BEX2 was overexpressed in advanced CRC from both the GSE14333 database and fresh C...

2014
Charlotta Lindwall Blom Lisa B. Mårtensson Lars B. Dahlin

We investigated (a) if activation of the mitogen activated protein kinase (MAPK) pathway was linked to the stress activated protein kinase (SAPK) pathway and (b) if JNK was required for activation of c-Jun in Schwann cells of rat sciatic nerve following injury. To this aim, ERK1/2 and the transcription factors c-Jun and ATF-3 were studied by immunohistochemistry in segments of transected nerves...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2010
Mark Kristiansen Rosie Hughes Pritika Patel Thomas S Jacques Andrew R Clark Jonathan Ham

Developing sympathetic neurons depend on NGF for survival. When sympathetic neurons are deprived of NGF in vitro, a well documented series of events, including c-Jun N-terminal kinase (JNK) pathway activation, release of cytochrome c from the mitochondria, and caspase activation, culminates in the death of the neuron by apoptosis within 24-48 h. This process requires de novo gene expression, su...

Journal: :Cell growth & differentiation : the molecular biology journal of the American Association for Cancer Research 2002
Stephanie Dehez Christiane Bierkamp Aline Kowalski-Chauvel Laurence Daulhac Chantal Escrieut Christiane Susini Lucien Pradayrol Daniel Fourmy Catherine Seva

The proliferative effects of gastrin on normal and malignant gastrointestinal tissues have been shown to be mediated by a G protein-coupled receptor (GPCR), the cholecystokinin B receptor. The c-Jun NH(2)-terminal kinase (JNK) pathway has been implicated in the regulation of mitogenesis by growth factors or cytokines. However, the contribution of this signaling cascade to the proliferative effe...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2001
X A Figueroa-Masot M Hetman M J Higgins N Kokot Z Xia

Bcl-2, an antiapoptotic protein, protects cells against many but not all forms of apoptosis. For example, Bcl-2 does not protect non-neuronal cells against taxol, a microtubule-stabilizing agent. The underlying mechanism for the ineffectiveness of Bcl-2 against taxol has been the subject of intense interest. Data from non-neuronal cells indicate that taxol-induced apoptosis requires activation ...

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