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.
Original language | English (US) |
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Pages (from-to) | 95-102 |
Number of pages | 8 |
Journal | Targeted Oncology |
Volume | 6 |
Issue number | 2 |
DOIs | |
State | Published - Jun 2011 |
Externally published | Yes |
Keywords
- Hypoxia
- Pediatric malignancies
- mTORC1 signaling
ASJC Scopus subject areas
- Pharmacology (medical)
- Oncology
- Cancer Research