Literature DB >> 33544134

Finding new edges: systems approaches to MTOR signaling.

Alexander Martin Heberle1,2, Ulrike Rehbein1,2,3, Maria Rodríguez Peiris1,3, Kathrin Thedieck1,2,3.   

Abstract

Cells have evolved highly intertwined kinase networks to finely tune cellular homeostasis to the environment. The network converging on the mechanistic target of rapamycin (MTOR) kinase constitutes a central hub that integrates metabolic signals and adapts cellular metabolism and functions to nutritional changes and stress. Feedforward and feedback loops, crosstalks and a plethora of modulators finely balance MTOR-driven anabolic and catabolic processes. This complexity renders it difficult - if not impossible - to intuitively decipher signaling dynamics and network topology. Over the last two decades, systems approaches have emerged as powerful tools to simulate signaling network dynamics and responses. In this review, we discuss the contribution of systems studies to the discovery of novel edges and modulators in the MTOR network in healthy cells and in disease.
© 2021 The Author(s).

Entities:  

Keywords:  amino acids; computational models; mechanistic target of rapamycin; protein kinase B; signaling; systems biology

Mesh:

Substances:

Year:  2021        PMID: 33544134      PMCID: PMC7924996          DOI: 10.1042/BST20190730

Source DB:  PubMed          Journal:  Biochem Soc Trans        ISSN: 0300-5127            Impact factor:   5.407


  126 in total

1.  Raptor, a binding partner of target of rapamycin (TOR), mediates TOR action.

Authors:  Kenta Hara; Yoshiko Maruki; Xiaomeng Long; Ken-ichi Yoshino; Noriko Oshiro; Sujuti Hidayat; Chiharu Tokunaga; Joseph Avruch; Kazuyoshi Yonezawa
Journal:  Cell       Date:  2002-07-26       Impact factor: 41.582

2.  mTOR complex-2 activates ENaC by phosphorylating SGK1.

Authors:  Ming Lu; Jian Wang; Kevin T Jones; Harlan E Ives; Morris E Feldman; Li-jun Yao; Kevan M Shokat; Kaveh Ashrafi; David Pearce
Journal:  J Am Soc Nephrol       Date:  2010-03-25       Impact factor: 10.121

3.  mTORC2 is required for proliferation and survival of TSC2-null cells.

Authors:  Elena A Goncharova; Dmitry A Goncharov; Hua Li; Wittaya Pimtong; Stephen Lu; Irene Khavin; Vera P Krymskaya
Journal:  Mol Cell Biol       Date:  2011-04-11       Impact factor: 4.272

4.  The tumor suppressor, PTEN/MMAC1, dephosphorylates the lipid second messenger, phosphatidylinositol 3,4,5-trisphosphate.

Authors:  T Maehama; J E Dixon
Journal:  J Biol Chem       Date:  1998-05-29       Impact factor: 5.157

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

6.  The role of AMPK and mTOR in nutrient sensing in pancreatic beta-cells.

Authors:  Catherine E Gleason; Danhong Lu; Lee A Witters; Christopher B Newgard; Morris J Birnbaum
Journal:  J Biol Chem       Date:  2007-02-07       Impact factor: 5.157

7.  Lysosomal recruitment of TSC2 is a universal response to cellular stress.

Authors:  Constantinos Demetriades; Monika Plescher; Aurelio A Teleman
Journal:  Nat Commun       Date:  2016-02-12       Impact factor: 14.919

8.  Cross-talks via mTORC2 can explain enhanced activation in response to insulin in diabetic patients.

Authors:  Rasmus Magnusson; Mika Gustafsson; Gunnar Cedersund; Peter Strålfors; Elin Nyman
Journal:  Biosci Rep       Date:  2017-01-24       Impact factor: 3.840

Review 9.  The Target of Rapamycin and Mechanisms of Cell Growth.

Authors:  Andrew R Tee
Journal:  Int J Mol Sci       Date:  2018-03-16       Impact factor: 5.923

Review 10.  Regulation of mTORC2 Signaling.

Authors:  Wenxiang Fu; Michael N Hall
Journal:  Genes (Basel)       Date:  2020-09-04       Impact factor: 4.096

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