نتایج جستجو برای: rapamycin

تعداد نتایج: 12061  

Journal: :Current Biology 2002

Journal: :Nature Reviews Neuroscience 2008

Journal: :JAMA dermatology 2015
Mari Wataya-Kaneda Mari Tanaka Lingli Yang Fei Yang Daisuke Tsuruta Ayumi Nakamura Shoji Matsumoto Toshimitsu Hamasaki Atushi Tanemura Ichiro Katayama

IMPORTANCE Tuberous sclerosis complex (TSC) is an autosomal dominant disorder leading to the aberrant activation of the mammalian target of rapamycin complex 1. Although the efficacy of mammalian target of rapamycin complex 1 inhibitors against tumors in patients with TSC, including facial angiofibroma, has been well investigated, their efficacy against hypomelanotic macules in patients with TS...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2012
Funda Meric-Bernstam Argun Akcakanat Huiqin Chen Kim-Anh Do Takafumi Sangai Farrell Adkins Ana Maria Gonzalez-Angulo Asif Rashid Katherine Crosby Mei Dong Alexandria T Phan Robert A Wolff Sanjay Gupta Gordon B Mills James Yao

PURPOSE We sought to determine whether phosphoinositide 3-kinase (PI3K) pathway mutation or activation state and rapamycin-induced feedback loop activation of Akt is associated with rapamycin sensitivity or resistance. EXPERIMENTAL DESIGN Cancer cell lines were tested for rapamycin sensitivity, Akt phosphorylation, and mTOR target inhibition. Mice injected with breast or neuroendocrine cancer...

2015
Angelika Kusch Maria Schmidt Dennis Gürgen Daniel Postpieszala Rusan Catar Björn Hegner Merci M. Davidson Shokoufeh Mahmoodzadeh Duska Dragun

Adaptive cardiac remodeling is characterized by enhanced signaling of mTORC2 downstream kinase Akt. In females, 17ß-estradiol (E2), as well as Akt contribute essentially to sex-related premenopausal cardioprotection. Pharmacologic mTOR targeting with rapamycin is increasingly used for various clinical indications, yet burdened with clinical heterogeneity in therapy responses. The drug inhibits ...

Journal: :Cardiovascular research 2005
Dalya Rosner Nicola McCarthy Martin Bennett

OBJECTIVE Drug-eluting stents containing the immunosuppressant rapamycin markedly inhibit in stent restenosis (ISR). However, the molecular mechanisms that underlie its effect on ISR-derived vascular smooth muscle cells (VSMCs), as opposed to normal VSMCs, are unknown. Specifically, as ISR-VSMCs have altered cell cycle regulation, rapamycin may arrest these cells via novel molecular pathways. ...

Journal: :Anticancer research 2012
Avinash L Mohan Marissa D Friedman D Ryan Ormond Michael Tobias Raj Murali Meena Jhanwar-Uniyal

Medulloblastoma is the most common malignant brain tumor in children. Recent studies have implicated sonic hedgehog (SHH) and insulin growth factor (IGF) as important mediators in deregulated pathways, which directly inactivate tuberous sclerosis complex, leading to activation of the serine/threonine kinase, mammalian target of rapamycin (mTOR). mTOR consists of two catalytic subunits of bioche...

2016
Geun-Kyung Lee Hyejin Shin Hyunjung Jade Lim

The mammalian target of rapamycin (mTOR) regulates cellular processes such as cell growth, metabolism, transcription, translation, and autophagy. Rapamycin is a selective inhibitor of mTOR, and induces autophagy in various systems. Autophagy contributes to clearance and recycling of macromolecules and organelles in response to stress. We previously reported that vitrified-warmed mouse oocytes s...

Journal: :Cell 1994
D M Sabatini H Erdjument-Bromage M Lui P Tempst S H Snyder

The immunosuppressants rapamycin and FK506 bind to the same intracellular protein, the immunophilin FKBP12. The FKB12-FK506 complex interacts with and inhibits the Ca(2+)-activated protein phosphatase calcineurin. The target of the FKBP12-rapamycin complex has not yet been identified. We report that a protein complex containing 245 kDa and 35 kDa components, designated rapamycin and FKBP12 targ...

Journal: :Blood 2004
Thomas Strömberg Anna Dimberg Anna Hammarberg Kristina Carlson Anders Osterborg Kenneth Nilsson Helena Jernberg-Wiklund

Circumvention of chemoresistance in the B-cell neoplasm multiple myeloma (MM) might be achieved by targeting certain intracellular signaling pathways crucial for survival of the malignant clone. The use of the macrolide rapamycin, selectively inhibiting the phosphoprotein mammalian target of rapamycin (mTOR) downstream of, for example, insulin-like growth factor-I receptor (IGF-IR), possibly re...

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