نتایج جستجو برای: rapamycin

تعداد نتایج: 12061  

Journal: :Indian Journal of Pharmaceutical Sciences 2023

To explore the function of kaempferol on lung cancer cell A549 and microRNA-199 variation is objective study. The proliferation was detected by counting kit-8. expression mammalian target rapamycin, phosphorylated light chain 3-?/?, beclin-1, B-cell lymphoma 2 2-associated X protein showed Western blot. determined quantitative polymerase reaction. adenocarcinomic human alveolar basal epithelial...

Journal: :Journal of Experimental Medicine 2005

Journal: :Archives of Dermatology 2010

2012
Zili Zhang Xiumei Wu Jie Duan David Hinrichs Keith Wegmann Gary L. Zhang Mark Hall James T. Rosenbaum

BACKGROUND Rapamycin, a potent immune modulator, is used to treat transplant rejection and some autoimmune diseases. Uveitis is a potentially severe inflammatory eye disease, and 2 clinical trials of treating uveitis with rapamycin are under way. Unexpectedly, recent research has demonstrated that low dose rapamycin enhances the memory T cell population and function. However, it is unclear how ...

Journal: :Molecular cancer research : MCR 2013
Onica Le Gendre Ayisha Sookdeo Stephie-Anne Duliepre Matthew Utter Maria Frias David A Foster

mTOR has been implicated in survival signals for many human cancers. Rapamycin and TGF-β synergistically induce G1 cell-cycle arrest in several cell lines with intact TGF-β signaling pathway, which protects cells from the apoptotic effects of rapamycin during S-phase of the cell cycle. Thus, rapamycin is cytostatic in the presence of serum/TGF-β and cytotoxic in the absence of serum. However, i...

Journal: :BMC Dermatology 2008
Aubrey Rauktys Nancy Lee Laifong Lee Sandra L Dabora

BACKGROUND Skin manifestations of Tuberous Sclerosis Complex (TSC) cause significant morbidity. The molecular mechanism underlying TSC is understood and there is evidence that systemic treatment with rapamycin or other mTOR inhibitors may be a useful approach to targeted therapy for the kidney and brain manifestations. Here we investigate topical rapamycin in a mouse model for TSC-related tumor...

Journal: :Cancer research 1999
H Hosoi M B Dilling T Shikata L N Liu L Shu R A Ashmun G S Germain R T Abraham P J Houghton

The mammalian target of rapamycin (mTOR) has been shown to link growth factor signaling and posttranscriptional control of translation of proteins that are frequently involved in cell cycle progression. However, the role of this pathway in cell survival has not been demonstrated. Here, we report that rapamycin, a specific inhibitor of mTOR kinase, induces G1 cell cycle arrest and apoptosis in t...

Journal: :Molecular cancer therapeutics 2016
Suman Mukhopadhyay Maria A Frias Amrita Chatterjee Paige Yellen David A Foster

The mTOR pathway is a critical regulator of cell growth, proliferation, metabolism, and survival. Dysregulation of mTOR signaling has been observed in most cancers and, thus, the mTOR pathway has been extensively studied for therapeutic intervention. Rapamycin is a natural product that inhibits mTOR with high specificity. However, its efficacy varies by dose in several contexts. First, differen...

Journal: :Cancer research 2009
Run-Qiang Chen Qing-Kai Yang Bing-Wen Lu Wei Yi Greg Cantin Yan-Ling Chen Colleen Fearns John R Yates Jiing-Dwan Lee

Because the mammalian target of rapamycin (mTOR) pathway is commonly deregulated in human cancer, mTOR inhibitors, rapamycin and its derivatives, are being actively tested in cancer clinical trials. Clinical updates indicate that the anticancer effect of these drugs is limited, perhaps due to rapamycin-dependent induction of oncogenic cascades by an as yet unclear mechanism. As such, we investi...

Journal: :Molecular cancer therapeutics 2012
Yan Liu Shi-Yong Sun Taofeek K Owonikoko Gabriel L Sica Walter J Curran Fadlo R Khuri Xingming Deng

Inhibition of mTOR signaling by rapamycin has been shown to activate extracellular signal-regulated kinase 1 or 2 (ERK1/2) and Akt in various types of cancer cells, which contributes to rapamycin resistance. However, the downstream effect of rapamycin-activated ERKs and Akt on survival or death substrate(s) remains unclear. We discovered that treatment of human lung cancer cells with rapamycin ...

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