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Publication : Stress and mTORture signaling.

First Author  Reiling JH Year  2006
Journal  Oncogene Volume  25
Issue  48 Pages  6373-83
PubMed ID  17041623 Mgi Jnum  J:320285
Mgi Id  MGI:6870986 Doi  10.1038/sj.onc.1209889
Citation  Reiling JH, et al. (2006) Stress and mTORture signaling. Oncogene 25(48):6373-83
abstractText  The TOR (target of rapamycin) pathway is an evolutionarily conserved signaling module regulating cell growth (accumulation of mass) in response to a variety of environmental cues such as nutrient availability, hypoxia, DNA damage and osmotic stress. Its pivotal role in cellular and organismal homeostasis is reflected in the fact that unrestrained signaling activity in mammals is associated with the occurrence of disease states including inflammation, cancer and diabetes. The existence of TOR homologs in unicellular organisms whose growth is affected by environmental factors, such as temperature, nutrients and osmolarity, suggests an ancient role for the TOR signaling network in the surveillance of stress conditions. Here, we will summarize recent advances in the TOR signaling field with special emphasis on how stress conditions impinge on insulin/insulin-like growth factor signaling/TOR signaling.
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