PTEN signaling in autism spectrum disorders DOI
Jing Zhou, Luis F. Parada

Current Opinion in Neurobiology, Journal Year: 2012, Volume and Issue: 22(5), P. 873 - 879

Published: June 2, 2012

Language: Английский

The many faces and functions of β-catenin DOI
Tomáš Valenta, George Hausmann, Konrad Basler

et al.

The EMBO Journal, Journal Year: 2012, Volume and Issue: 31(12), P. 2714 - 2736

Published: May 22, 2012

Language: Английский

Citations

1421

Activators and Inhibitors of NRF2: A Review of Their Potential for Clinical Development DOI Creative Commons

Natalia Robledinos-Antón,

Raquel Fernández-Ginés,

Gina Manda

et al.

Oxidative Medicine and Cellular Longevity, Journal Year: 2019, Volume and Issue: 2019, P. 1 - 20

Published: July 14, 2019

The transcription factor NRF2 (nuclear erythroid 2-related 2) triggers the first line of homeostatic responses against a plethora environmental or endogenous deviations in redox metabolism, proteostasis, inflammation, etc. Therefore, pharmacological activation is promising therapeutic approach for several chronic diseases that are underlined by oxidative stress and such as neurodegenerative, cardiovascular, metabolic diseases. A particular case cancer, where confers survival advantage to constituted tumors, therefore, inhibition desired. This review describes electrophilic nonelectrophilic activators with clinical projection various We also analyze status inhibitors, which at this time provide proof concept blocking activity cancer therapy.

Language: Английский

Citations

528

GSK-3 as potential target for therapeutic intervention in cancer DOI Open Access
James A. McCubrey,

Linda S. Steelman,

Fred E. Bertrand

et al.

Oncotarget, Journal Year: 2014, Volume and Issue: 5(10), P. 2881 - 2911

Published: May 28, 2014

// James A. McCubrey 1 , Linda S. Steelman Fred E. Bertrand 2 Nicole M. Davis Melissa Sokolosky Steve L. Abrams Giuseppe Montalto 3 Antonino B. D’Assoro 4 Massimo Libra 5 Ferdinando Nicoletti Roberta Maestro 6 Jorg Basecke 7,8 Dariusz Rakus 9 Agnieszka Gizak Zoya Demidenko 10 Lucio Cocco 11 Alberto Martelli and Melchiorre Cervello 12 Department of Microbiology Immunology, Brody School Medicine at East Carolina University Greenville, NC, USA Oncology, Brody Biomedical Internal Specialties, Palermo, Italy Medical Mayo Clinic Cancer Center, Rochester, MN, Bio-Medical Sciences, Catania, Experimental Oncology 1, CRO IRCCS, National Institute, Aviano, Pordenone, Italy. 7 Medicine, Göttingen, Germany 8 Sanct-Josef-Hospital Cloppenburg, Hematology Animal Molecular Physiology, Institute Biology, Wroclaw University, Wroclaw, Poland Cell Stress Roswell Park Buffalo, NY, Dipartimento di Scienze Biomediche e Neuromotorie, Università Bologna, Consiglio Nazionale delle Ricerche, Istituto Biomedicina Immunologia Molecolare “Alberto Monroy”, Correspondence: McCubrey, email: Keywords : GSK-3, cancer stem cells, Wnt/beta-catenin, PI3K, Akt, mTOR, Hedgehog, Notch, Targeted Therapy, Therapy Resistance, Mutations, Rapamycin Received April 24, 2014 Accepted May 28, Published Abstract The serine/threonine kinase glycogen synthase kinase-3 (GSK-3) was initially identified studied in the regulation synthesis. GSK-3 functions a wide range cellular processes. Aberrant activity has been implicated many human pathologies including: bipolar depression, Alzheimer’s disease, Parkinson’s cancer, non-insulin-dependent diabetes mellitus (NIDDM) others. In some cases, suppression by phosphorylation Akt other kinases associated with progression. these tumor suppressor functions. progression stabilizing components beta-catenin complex. situations, oncogenic properties. While inhibitors to have developed, their use remains controversial because ambiguous role development. this review, we will focus on diverse roles that plays various cancers, particular solid tumors. Recently, also generation cells cell types. We discuss how pivotal interacts multiple signaling pathways such as: PI3K/PTEN/Akt/mTORC1, Ras/Raf/MEK/ERK, Notch

Language: Английский

Citations

455

GSK3 and its interactions with the PI3K/AKT/mTOR signalling network DOI
Miguel A. Hermida, J. Dinesh Kumar, Nicholas R. Leslie

et al.

Advances in Biological Regulation, Journal Year: 2017, Volume and Issue: 65, P. 5 - 15

Published: June 27, 2017

Language: Английский

Citations

393

Rapid induction and long-term self-renewal of primitive neural precursors from human embryonic stem cells by small molecule inhibitors DOI Open Access
Wenlin Li, Woong Sun, Yu Zhang

et al.

Proceedings of the National Academy of Sciences, Journal Year: 2011, Volume and Issue: 108(20), P. 8299 - 8304

Published: April 27, 2011

Human embryonic stem cells (hESCs) hold enormous promise for regenerative medicine. Typically, hESC-based applications would require their in vitro differentiation into a desirable homogenous cell population. A major challenge of the current hESC paradigm is inability to effectively capture and, long-term, stably expand primitive lineage-specific stem/precursor that retain broad potential more importantly, developmental stage-specific propensity. Here, we report synergistic inhibition glycogen synthase kinase 3 (GSK3), transforming growth factor β (TGF-β), and Notch signaling pathways by small molecules can efficiently convert monolayer cultured hESCs neuroepithelium within 1 wk under chemically defined condition. These neuroepithelia self-renew presence leukemia inhibitory factor, GSK3 inhibitor (CHIR99021), TGF-β receptor (SB431542); high neurogenic responsiveness instructive neural patterning cues toward midbrain hindbrain neuronal subtypes; exhibit vivo integration. Our work uniformly captures maintains from hESCs.

Language: Английский

Citations

353

GSK-3 Inhibitors: Preclinical and Clinical Focus on CNS DOI Creative Commons
Hagit Eldar-Finkelman, Ana Martı́nez

Frontiers in Molecular Neuroscience, Journal Year: 2011, Volume and Issue: 4

Published: Jan. 1, 2011

Inhibiting glycogen synthase kinase-3 (GSK-3) activity via pharmacological intervention has become an important strategy for treating neurodegenerative and psychiatric disorders. The known GSK-3 inhibitors are of diverse chemotypes mechanisms action include compounds isolated from natural sources, cations, synthetic small-molecule ATP-competitive inhibitors, non-ATP-competitive substrate-competitive inhibitors. Here we describe the variety with a specific emphasis on their biological activities in neurons neurological We further highlight our current progress development GSK-3. available data raise hope that one or more these drug design approaches will prove successful at stabilizing even reversing aberrant neuropathology cognitive deficits certain central nervous system

Language: Английский

Citations

324

Sculpting Neural Circuits by Axon and Dendrite Pruning DOI Open Access
Martin M. Riccomagno, Alex L. Kolodkin

Annual Review of Cell and Developmental Biology, Journal Year: 2015, Volume and Issue: 31(1), P. 779 - 805

Published: Oct. 5, 2015

The assembly of functional neural circuits requires the combined action progressive and regressive events. Regressive events encompass a variety inhibitory developmental processes, including axon dendrite pruning, which facilitate removal exuberant neuronal connections. Most pruning involves axons that had already made synaptic connections; thus, is tightly associated with synapse elimination. In many instances, these processes are regulated by interplay between neurons glial cells act instructively during remodeling. Owing to importance dendritic remodeling require precise spatial temporal control, this achieved range distinct molecular mechanisms. Disruption mechanisms results in abnormal has been linked brain dysfunction. Therefore, understanding will be instrumental advancing our knowledge disease mental disorders.

Language: Английский

Citations

317

A Small Molecule Screen in Stem-Cell-Derived Motor Neurons Identifies a Kinase Inhibitor as a Candidate Therapeutic for ALS DOI Creative Commons
Yin Yang, Shailesh Gupta, Kevin J. Kim

et al.

Cell stem cell, Journal Year: 2013, Volume and Issue: 12(6), P. 713 - 726

Published: April 18, 2013

Language: Английский

Citations

293

How to make a midbrain dopaminergic neuron DOI Creative Commons
Ernest Arenas, Mark Denham, J. Carlos Villaescusa

et al.

Development, Journal Year: 2015, Volume and Issue: 142(11), P. 1918 - 1936

Published: May 26, 2015

ABSTRACT Midbrain dopaminergic (mDA) neuron development has been an intense area of research during recent years. This is due in part to a growing interest regenerative medicine and the hope that treatment for diseases affecting mDA neurons, such as Parkinson's disease (PD), might be facilitated by better understanding how these neurons are specified, differentiated maintained vivo. knowledge help instruct efforts generate vitro, which holds promise not only cell replacement therapy, but also modeling drug discovery. In this Primer, we will focus on developments molecular mechanisms regulate vivo, they have used human vitro from pluripotent stem cells or somatic via direct reprogramming. Current challenges future avenues PD identified discussed.

Language: Английский

Citations

292

Small Molecules Efficiently Reprogram Human Astroglial Cells into Functional Neurons DOI Creative Commons
Lei Zhang,

Jiu-Chao Yin,

Hana Yeh

et al.

Cell stem cell, Journal Year: 2015, Volume and Issue: 17(6), P. 735 - 747

Published: Oct. 23, 2015

Language: Английский

Citations

262