نتایج جستجو برای: akt

تعداد نتایج: 40794  

Journal: :The Journal of biological chemistry 2011
You-Tong Wu Weiming Ouyang Adam S Lazorchak Dou Liu Han-Ming Shen Bing Su

The protein kinase Akt (also known as protein kinase B) is a critical signaling hub downstream of various cellular stimuli such as growth factors that control cell survival, growth, and proliferation. The activity of Akt is tightly regulated, and the aberrant activation of Akt is associated with diverse human diseases including cancer. Although it is well documented that the mammalian target of...

2009
Tatsuya Okuzumi Dorothea Fiedler Chao Zhang Daniel C. Gray Brian Aizenstein Randy Hoffman Kevan M. Shokat

The kinase Akt plays a central role as a regulator of multiple growth factor input signals, thus making it an attractive anticancer drug target. A-443654 is an ATP-competitive Akt inhibitor. Unexpectedly, treatment of cells with A-443654 causes paradoxical hyperphosphorylation of Akt at its two regulatory sites (Thr308 and Ser473). We explored whether inhibitor-induced hyperphosphorylation of A...

Journal: :Cancer research 2001
J Brognard A S Clark Y Ni P A Dennis

To evaluate the role of Akt/PKB in non-small cell lung cancer (NSCLC) survival, we analyzed NSCLC cell lines that differed in tumor histology as well as p53, Rb, and K-ras status. Constitutive Akt/protein kinase B (PKB) activity was demonstrated in 16 of 17 cell lines by maintenance of S473 phosphorylation with serum deprivation. Additional analysis of five of 2these NSCLC lines revealed that p...

Journal: :research in pharmaceutical sciences 0
parham reisi 1department of physiology, school of medicine, isfahan university of medical sciences, isfahan, i.r. iran. nastaran eidelkhani 1department of physiology, school of medicine, isfahan university of medical sciences, isfahan, i.r. iran. laleh rafiee 2applied physiology research center, isfahan university of medical sciences, isfahan, i.r. iran. mohammad kazemi 3department of genetics and molecular biology, school of medicine, isfahan university of medical sciences, isfahan, i.r. iran. maryam radahmadi 1department of physiology, school of medicine, isfahan university of medical sciences, isfahan, i.r. iran. hojjatallah alaei 1department of physiology, school of medicine, isfahan university of medical sciences, isfahan, i.r. iran.

stress is one of the effective factors in the development of depressive disorders that performs some parts of its effects by affecting hippocampus. since doxepin has been shown to have neuroprotective effects, in this study, we focused on the effects of doxepin on the expression of involved genes in neuronal survival and plasticity in the rat hippocampus following chronic stress. male wistar ra...

Journal: :American journal of physiology. Cell physiology 2007
Hiraku Ono Hideyuki Sakoda Midori Fujishiro Motonobu Anai Akifumi Kushiyama Yasushi Fukushima Hideki Katagiri Takehide Ogihara Yoshitomo Oka Hideaki Kamata Nanao Horike Yasunobu Uchijima Hiroki Kurihara Tomoichiro Asano

Carboxy-terminal modulator protein (CTMP) was identified as binding to the carboxy terminus of Akt and inhibiting the phosphorylation and activation of Akt. In contrast to a previous study, we found CTMP overexpression to significantly enhance Akt phosphorylation at both Thr(308) and Ser(473) as well as the kinase activity of Akt, while phosphatidylinositol 3-kinase (PI3-kinase) activity was un...

2013
Natalia Dünner Carolina Quezada F. Andrés Berndt José Cánovas Cecilia V. Rojas

The renin-angiotensin system expressed in adipose tissue has been implicated in the modulation of adipocyte formation, glucose metabolism, triglyceride accumulation, lipolysis, and the onset of the adverse metabolic consequences of obesity. As we investigated angiotensin II signal transduction mechanisms in human preadipose cells, an interplay of extracellular-signal-regulated kinases 1 and 2 (...

Journal: :Cancer research 2003
Wanping Xu Xitong Yuan Yun Jin Jung Yongping Yang Andrea Basso Neal Rosen Eun Joo Chung Jane Trepel Len Neckers

AKT, a serine/threonine kinase that promotes cell survival, can be activated by overexpression of the receptor tyrosine kinase ErbB2. Conversely, down-regulation of ErbB2 inhibits AKT activation. Here, we identify PP1 as a serine/threonine phosphatase that associates with and dephosphorylates AKT in breast cancer cells, and we show that ErbB2 inhibits PP1-dependent dephosphorylation of AKT. Inh...

Amaral L Lucas T Porto C Quintas LE,

Background: Novel roles for the interaction of cardiotonic steroids to Na+/K+-ATPase have been established in recent years. The aim of the present study was to investigate the intracellular signaling events downstream the action of ouabain on Na+/K+-ATPase in Sertoli cell obtained from immature rats. Treatment of Sertoli cells with ouabain (1 μM) induced a rapid and transient increase in the ex...

Journal: :General Physiology and Biophysics 2021

Successful implantation requires endometrial receptivity. To investigate the mechanisms of miR-494-3p on receptivity, GnRHa's superovulation scheme was designed to reduce and pregnant mice were injected with antagomir. The regulatory role identified by RT-qPCR, uterine blastocyst count, scanning electron microscopy, hematoxylin-eosin (HE) staining, Western blot. Results indicated that antagomir...

Journal: :Molecular and cellular biology 2009
Jixin Ding Keyong Du

Akt is activated on the plasma membrane and its substrates are distributed throughout various cellular compartments. To phosphorylate its substrates, Akt needs to be recruited to specific intracellular compartments. Thus, regulation of Akt cellular compartmentalization constitutes an important mechanism to specify Akt signaling. Here, we report the identification of ClipR-59 as an Akt interacti...

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