نتایج جستجو برای: hsp90

تعداد نتایج: 5774  

Journal: :The Journal of biological chemistry 2004
Jennifer E Whittier Yijia Xiong Martin C Rechsteiner Thomas C Squier

The 20 S proteasome has been suggested to play a critical role in mediating the degradation of abnormal proteins under conditions of oxidative stress and has been found in tight association with the molecular chaperone Hsp90. To elucidate the role of Hsp90 in promoting the degradation of oxidized calmodulin (CaM(ox)), we have purified red blood cell 20 S proteasomes free of Hsp90 and assessed t...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2014
Rahul S Samant Paul A Clarke Paul Workman

The molecular chaperone heat shock protein 90 (HSP90) is required for the activity and stability of its client proteins. Pharmacologic inhibition of HSP90 leads to the ubiquitin-mediated degradation of clients, particularly activated or mutant oncogenic protein kinases. Client ubiquitination occurs via the action of one or more E3 ubiquitin ligases. We sought to identify the role of Cullin-RING...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2008
Margaret K Callahan Manish Garg Pramod K Srivastava

CD8(+) T cells recognize peptide fragments of endogenously synthesized antigens of cancers or viruses, presented by MHC I molecules. Such antigen presentation requires the generation of peptides in the cytosol, their passage to the endoplasmic reticulum, loading of MHC I with peptides, and transport of MHC I-peptide complexes to the cell surface. Heat-shock protein (hsp) 90 is a cytosolic chape...

Journal: :International journal of clinical and experimental pathology 2015
Yongkai Wu Bo Huang Qian Liu Yongyu Liu

Heat shock protein 90-beta (Hsp90-β) is associated with cell proliferation, differentiation and apoptosis and has been investigated as a prognostic factor in many cancers. However, Hsp90-β protein expression in lung adenocarcinoma (ADC) has not been thoroughly elucidated. The aim of this study was to determine the relationship between Hsp90-β expression, clinicopathological parameters and progn...

Journal: :Arteriosclerosis, thrombosis, and vascular biology 2012
Fanny Desjardins Chantal Delisle Jean-Philippe Gratton

OBJECTIVE Vascular endothelial growth factor (VEGF) signaling to endothelial NO synthase (eNOS) plays a central role in angiogenesis. In endothelial cells (ECs), heat-shock protein 90 (Hsp90) is also a regulator of eNOS activity. Our study is designed to determine whether modulation of the activator of Hsp90 ATPase 1 (AHA1) regulates the function of Hsp90 in ECs. METHODS AND RESULTS We show t...

2009
Sheena D. Singh Nicole Robbins Aimee K. Zaas Wiley A. Schell John R. Perfect Leah E. Cowen

Candida albicans is the leading fungal pathogen of humans, causing life-threatening disease in immunocompromised individuals. Treatment of candidiasis is hampered by the limited number of antifungal drugs whose efficacy is compromised by host toxicity, fungistatic activity, and the emergence of drug resistance. We previously established that the molecular chaperone Hsp90, which regulates the fo...

Journal: :American journal of physiology. Cell physiology 2011
Suxin Luo Tingting Wang Honghua Qin Han Lei Yong Xia

Inducible nitric oxide (NO) synthase (iNOS) plays an important role in cell injury and host defense. While undetectable in normal tissues, iNOS expression is induced by endotoxins and inflammatory cytokines primarily via the IκB kinase/nuclear factor-κB (IKK-NF-κB) and Janus kinase (JAK)-signal transducers and activators of transcription 1 (STAT1) pathways. Our previous studies found that heat ...

Journal: :The Journal of biological chemistry 2006
Anna C Y Fan Melanie K Bhangoo Jason C Young

The Tom70 import receptor on the mitochondrial outer membrane specifically recognizes Hsp90 and Hsc70, a critical step for the import of mitochondrial preproteins, the targeting of which depends on these cytosolic chaperones. To analyze the role of Hsp90 in mitochondrial import, the effects of the Hsp90 inhibitors geldanamycin and novobiocin were compared. Geldanamycin occludes the N-terminal A...

Journal: :Blood 2005
Januario E Castro Carlos E Prada Olivier Loria Adeela Kamal Liguang Chen Francis J Burrows Thomas J Kipps

The zeta-associated protein of 70 kDa (ZAP-70) is expressed in patients with aggressive chronic lymphocytic leukemia (CLL). We found that ZAP-70+ CLL cells expressed activated heat-shock protein 90 (Hsp90) with high binding affinity for Hsp90 inhibitors, such as 17-allyl-amino-demethoxy-geldanamycin (17-AAG), whereas normal lymphocytes or ZAP-70- CLL cells expressed nonactivated Hsp90. Activate...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2006
Lata T Gooljarsingh Christine Fernandes Kang Yan Hong Zhang Michael Grooms Kyung Johanson Robert H Sinnamon Robert B Kirkpatrick John Kerrigan Tia Lewis Marc Arnone Alastair J King Zhihong Lai Robert A Copeland Peter J Tummino

Heat shock protein (Hsp)90 is emerging as an important therapeutic target for the treatment of cancer. Two analogues of the Hsp90 inhibitor geldanamycin are currently in clinical trials. Geldanamycin (GA) and its analogues have been reported to bind purified Hsp90 with low micromolar potency, in stark contrast to their low nanomolar antiproliferative activity in cell culture and their potent an...

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