Literature DB >> 20561505

Molecular imaging of glycogen synthase kinase-3beta and casein kinase-1alpha kinases.

Shyam Nyati1, Rajesh Ranga, Brian D Ross, Alnawaz Rehemtulla, Mahaveer Swaroop Bhojani.   

Abstract

Glycogen synthase kinase-3beta (GSK3beta) and casein kinase-1alpha (CK1alpha) are multifunctional kinases that play critical roles in the regulation of a number of cellular processes. In spite of their importance, molecular imaging tools for noninvasive and real-time monitoring of their kinase activities have not been devised. Here we report development of the bioluminescent GSK3beta and CK1alpha reporter (BGCR) based on firefly luciferase complementation. Treatment of SW620 cells stably expressing the reporter with inhibitors of GSK3beta (SB415286 and LiCl) or CK1alpha (CKI-7) resulted in dose- and time-dependent increases in BGCR activity that were validated using Western blotting. No increase in bioluminescence was observed in the case of S37A mutant (GSK3beta inhibitors) or S45A mutant (CKI-7), demonstrating the specificity of the reporter. Imaging of mice tumor xenograft generated with BGCR-expressing SW620 cells following treatment with LiCl showed unique oscillations in GSK3beta activity that were corroborated by phosphorylated GSK3beta immunoblotting. Taken together, the BGCR is a novel molecular imaging tool that reveals unique insight into GSK3beta and CK1alpha kinase activities and may provide a powerful tool in experimental therapeutics for rapid optimization of dose and schedule of targeted therapies and for monitoring therapeutic response. Copyright 2010 Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20561505      PMCID: PMC2922438          DOI: 10.1016/j.ab.2010.06.020

Source DB:  PubMed          Journal:  Anal Biochem        ISSN: 0003-2697            Impact factor:   3.365


  54 in total

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Review 3.  The paradoxical pro- and anti-apoptotic actions of GSK3 in the intrinsic and extrinsic apoptosis signaling pathways.

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5.  Lrp5-independent activation of Wnt signaling by lithium chloride increases bone formation and bone mass in mice.

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Journal:  Nature       Date:  2005-03-31       Impact factor: 49.962

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9.  Ser-557-phosphorylated mCRY2 is degraded upon synergistic phosphorylation by glycogen synthase kinase-3 beta.

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  10 in total

1.  Molecular imaging of akt enables early prediction of response to molecular targeted therapy.

Authors:  Mahaveer S Bhojani; Mukesh K Nyati; Lili Zhao; Daniel P Normolle; Brian D Ross; Theodore S Lawrence; Alnawaz Rehemtulla
Journal:  Transl Oncol       Date:  2011-06-01       Impact factor: 4.243

2.  Quantitative and Dynamic Imaging of ATM Kinase Activity by Bioluminescence Imaging.

Authors:  Shyam Nyati; Grant Young; Brian Dale Ross; Alnawaz Rehemtulla
Journal:  Methods Mol Biol       Date:  2017

3.  Molecular imaging of TGFβ-induced Smad2/3 phosphorylation reveals a role for receptor tyrosine kinases in modulating TGFβ signaling.

Authors:  Shyam Nyati; Katrina Schinske; Dipankar Ray; Mukesh K Nyati; Mukesh Nyati; Brian Dale Ross; Alnawaz Rehemtulla
Journal:  Clin Cancer Res       Date:  2011-09-26       Impact factor: 12.531

4.  A novel kinase inhibitor of FADD phosphorylation chemosensitizes through the inhibition of NF-κB.

Authors:  Katrina A Schinske; Shyam Nyati; Amjad P Khan; Terence M Williams; Timothy D Johnson; Brian D Ross; Ricardo Pérez Tomás; Alnawaz Rehemtulla
Journal:  Mol Cancer Ther       Date:  2011-08-22       Impact factor: 6.261

5.  Quantitative and Dynamic Imaging of ATM Kinase Activity.

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Journal:  Methods Mol Biol       Date:  2017

6.  Luminescent kinase activity biosensors based on a versatile bimolecular switch.

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7.  Novel molecular imaging platform for monitoring oncological kinases.

Authors:  Shyam Nyati; Brian D Ross; Alnawaz Rehemtulla; Mahaveer S Bhojani
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Review 8.  Luciferase fragment complementation imaging in preclinical cancer studies.

Authors:  Madryn C Lake; Eric O Aboagye
Journal:  Oncoscience       Date:  2014-06-01

Review 9.  Casein kinase 1α: biological mechanisms and theranostic potential.

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  10 in total

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