Literature DB >> 33910214

Current Approaches and Future Directions for the Treatment of mTORopathies.

Vasiliki Karalis1, Helen S Bateup1,2,3.   

Abstract

The mechanistic target of rapamycin (mTOR) is a kinase at the center of an evolutionarily conserved signaling pathway that orchestrates cell growth and metabolism. mTOR responds to an array of intra- and extracellular stimuli and in turn controls multiple cellular anabolic and catabolic processes. Aberrant mTOR activity is associated with numerous diseases, with particularly profound impact on the nervous system. mTOR is found in two protein complexes, mTOR complex 1 (mTORC1) and 2 (mTORC2), which are governed by different upstream regulators and have distinct cellular actions. Mutations in genes encoding for mTOR regulators result in a collection of neurodevelopmental disorders known as mTORopathies. While these disorders can affect multiple organs, neuropsychiatric conditions such as epilepsy, intellectual disability, and autism spectrum disorder have a major impact on quality of life. The neuropsychiatric aspects of mTORopathies have been particularly challenging to treat in a clinical setting. Current therapeutic approaches center on rapamycin and its analogs, drugs that are administered systemically to inhibit mTOR activity. While these drugs show some clinical efficacy, adverse side effects, incomplete suppression of mTOR targets, and lack of specificity for mTORC1 or mTORC2 may limit their utility. An increased understanding of the neurobiology of mTOR and the underlying molecular, cellular, and circuit mechanisms of mTOR-related disorders will facilitate the development of improved therapeutics. Animal models of mTORopathies have helped unravel the consequences of mTOR pathway mutations in specific brain cell types and developmental stages, revealing an array of disease-related phenotypes. In this review, we discuss current progress and potential future directions for the therapeutic treatment of mTORopathies with a focus on findings from genetic mouse models.
© 2021 The Author(s) Published by S. Karger AG, Basel.

Entities:  

Keywords:  Epilepsy; Neurodevelopmental disorders; PTEN; Rapamycin; Raptor; Rictor; Tuberous sclerosis complex; mTORC1; mTORC2; mTORopathy

Mesh:

Substances:

Year:  2021        PMID: 33910214      PMCID: PMC8440338          DOI: 10.1159/000515672

Source DB:  PubMed          Journal:  Dev Neurosci        ISSN: 0378-5866            Impact factor:   2.984


  186 in total

1.  Loss of mTOR-dependent macroautophagy causes autistic-like synaptic pruning deficits.

Authors:  Guomei Tang; Kathryn Gudsnuk; Sheng-Han Kuo; Marisa L Cotrina; Gorazd Rosoklija; Alexander Sosunov; Mark S Sonders; Ellen Kanter; Candace Castagna; Ai Yamamoto; Zhenyu Yue; Ottavio Arancio; Bradley S Peterson; Frances Champagne; Andrew J Dwork; James Goldman; David Sulzer
Journal:  Neuron       Date:  2014-08-21       Impact factor: 17.173

2.  Identification of TBC7 having TBC domain as a novel binding protein to TSC1-TSC2 complex.

Authors:  Akio Nakashima; Ken-ichi Yoshino; Takafumi Miyamoto; Satoshi Eguchi; Noriko Oshiro; Ushio Kikkawa; Kazuyoshi Yonezawa
Journal:  Biochem Biophys Res Commun       Date:  2007-07-16       Impact factor: 3.575

3.  Somatic Mutations in TSC1 and TSC2 Cause Focal Cortical Dysplasia.

Authors:  Jae Seok Lim; Ramu Gopalappa; Se Hoon Kim; Suresh Ramakrishna; Minji Lee; Woo-Il Kim; Junho Kim; Sang Min Park; Junehawk Lee; Jung-Hwa Oh; Heung Dong Kim; Chang-Hwan Park; Joon Soo Lee; Sangwoo Kim; Dong Seok Kim; Jung Min Han; Hoon-Chul Kang; Hyongbum Henry Kim; Jeong Ho Lee
Journal:  Am J Hum Genet       Date:  2017-02-16       Impact factor: 11.025

4.  TBC1D7 mutations are associated with intellectual disability, macrocrania, patellar dislocation, and celiac disease.

Authors:  Ali Abdullah Alfaiz; Lucia Micale; Barbara Mandriani; Bartolomeo Augello; Maria Teresa Pellico; Jacqueline Chrast; Ioannis Xenarios; Leopoldo Zelante; Giuseppe Merla; Alexandre Reymond
Journal:  Hum Mutat       Date:  2014-04       Impact factor: 4.878

5.  Tti1 and Tel2 are critical factors in mammalian target of rapamycin complex assembly.

Authors:  Takeshi Kaizuka; Taichi Hara; Noriko Oshiro; Ushio Kikkawa; Kazuyoshi Yonezawa; Kenji Takehana; Shun-Ichiro Iemura; Tohru Natsume; Noboru Mizushima
Journal:  J Biol Chem       Date:  2010-04-28       Impact factor: 5.157

Review 6.  Regulation of translation initiation by FRAP/mTOR.

Authors:  A C Gingras; B Raught; N Sonenberg
Journal:  Genes Dev       Date:  2001-04-01       Impact factor: 11.361

7.  mTOR controls cell cycle progression through its cell growth effectors S6K1 and 4E-BP1/eukaryotic translation initiation factor 4E.

Authors:  Diane C Fingar; Celeste J Richardson; Andrew R Tee; Lynn Cheatham; Christina Tsou; John Blenis
Journal:  Mol Cell Biol       Date:  2004-01       Impact factor: 4.272

8.  Response of a neuronal model of tuberous sclerosis to mammalian target of rapamycin (mTOR) inhibitors: effects on mTORC1 and Akt signaling lead to improved survival and function.

Authors:  Lynsey Meikle; Kristen Pollizzi; Anna Egnor; Ioannis Kramvis; Heidi Lane; Mustafa Sahin; David J Kwiatkowski
Journal:  J Neurosci       Date:  2008-05-21       Impact factor: 6.167

9.  Mutations causing syndromic autism define an axis of synaptic pathophysiology.

Authors:  Benjamin D Auerbach; Emily K Osterweil; Mark F Bear
Journal:  Nature       Date:  2011-11-23       Impact factor: 49.962

10.  A small molecule inhibitor of Rheb selectively targets mTORC1 signaling.

Authors:  Sarah J Mahoney; Sridhar Narayan; Lisa Molz; Lauren A Berstler; Seong A Kang; George P Vlasuk; Eddine Saiah
Journal:  Nat Commun       Date:  2018-02-07       Impact factor: 14.919

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  11 in total

1.  Dopamine neuron morphology and output are differentially controlled by mTORC1 and mTORC2.

Authors:  Polina Kosillo; Kamran M Ahmed; Erin E Aisenberg; Vasiliki Karalis; Bradley M Roberts; Stephanie J Cragg; Helen S Bateup
Journal:  Elife       Date:  2022-07-26       Impact factor: 8.713

2.  TAU ablation in excitatory neurons and postnatal TAU knockdown reduce epilepsy, SUDEP, and autism behaviors in a Dravet syndrome model.

Authors:  Eric Shao; Che-Wei Chang; Zhiyong Li; Xinxing Yu; Kaitlyn Ho; Michelle Zhang; Xin Wang; Jeffrey Simms; Iris Lo; Jessica Speckart; Julia Holtzman; Gui-Qiu Yu; Erik D Roberson; Lennart Mucke
Journal:  Sci Transl Med       Date:  2022-04-27       Impact factor: 19.319

3.  Impact of Raptor and Rictor Deletion on Hippocampal Pathology Following Status Epilepticus.

Authors:  Christin M Godale; Emma V Parkins; Christina Gross; Steve C Danzer
Journal:  J Mol Neurosci       Date:  2022-05-27       Impact factor: 2.866

Review 4.  Monitoring and Managing Patients with Tuberous Sclerosis Complex: Current State of Knowledge.

Authors:  Inês Gomes; Joana Jesus Ribeiro; Filipe Palavra
Journal:  J Multidiscip Healthc       Date:  2022-07-14

5.  Early Human Postnatal Brain Development Through the Lens of Rare Genetic Disorders.

Authors:  Eric M Morrow
Journal:  Biol Psychiatry       Date:  2021-09-01       Impact factor: 12.810

Review 6.  Dysregulation of mTOR Signaling after Brain Ischemia.

Authors:  Mario Villa-González; Gerardo Martín-López; María José Pérez-Álvarez
Journal:  Int J Mol Sci       Date:  2022-03-04       Impact factor: 5.923

7.  PARVing the Way to Cap Translation for Seizure Control.

Authors:  Christina Gross
Journal:  Epilepsy Curr       Date:  2021-06-27       Impact factor: 7.500

8.  Whole Exome Sequencing in 16p13.11 Microdeletion Patients Reveals New Variants Through Deductive and Systems Medicine Approaches.

Authors:  Paola Granata; Dario Cocciadiferro; Alessandra Zito; Chiara Pessina; Alessandro Bassani; Fabio Zambonin; Antonio Novelli; Mauro Fasano; Rosario Casalone
Journal:  Front Genet       Date:  2022-03-15       Impact factor: 4.599

9.  The Cyanotoxin 2,4-DAB Reduces Viability and Causes Behavioral and Molecular Dysfunctions Associated with Neurodegeneration in Larval Zebrafish.

Authors:  Rubia M Martin; Michael S Bereman; Kurt C Marsden
Journal:  Neurotox Res       Date:  2022-01-14       Impact factor: 3.978

Review 10.  Modeling Somatic Mutations Associated With Neurodevelopmental Disorders in Human Brain Organoids.

Authors:  Bipan K Deb; Helen S Bateup
Journal:  Front Mol Neurosci       Date:  2022-01-04       Impact factor: 5.639

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