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Targeted Oncology

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01.06.2011 | Review

Regulation of mammalian target of rapamycin complex 1 (mTORC1) by hypoxia: causes and consequences

verfasst von: Hakan Cam, Peter J. Houghton

Erschienen in: Targeted Oncology | Ausgabe 2/2011

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Abstract

Integration of cellular and extracellular signals maintains tissue homeostasis under conditions of normal proliferation and stress. A central player in regulating responses to stress is the serine/threonine kinase mammalian target of rapamycin (mTOR). In many cancers, mTOR complex 1 (mTORC1) signaling is enhanced, even under conditions where such signaling should be suppressed. This article reviews some of the details that are emerging on how low oxygen (hypoxia) regulates mTORC1 signaling, and the consequences for dysregulation in pediatric solid tumors.

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Titel: Regulation of mammalian target of rapamycin complex 1 (mTORC1) by hypoxia: causes and consequences
verfasst von: Hakan Cam
Peter J. Houghton
Publikationsdatum: 01.06.2011
Verlag: Springer-Verlag
Erschienen in: Targeted Oncology / Ausgabe 2/2011
Print ISSN: 1776-2596
Elektronische ISSN: 1776-260X
DOI: https://doi.org/10.1007/s11523-011-0173-x

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Regulation of mammalian target of rapamycin complex 1 (mTORC1) by hypoxia: causes and consequences

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