Abstract:
:Rapamycin analogs that inhibit mTOR signaling have antitumor activity against certain lymphomas, but treatment of solid tumors has been less encouraging despite inhibition of mTOR function. Two recent papers give insight into the potential use of mTOR inhibitors. O'Reilly et al. provide evidence that poor tumor response to rapamycins is the result of relieving mTOR-mediated feedback inhibition of insulin receptor substrate 1, and activation of Akt-mediated survival. In the second paper, Kaper et al. address the impact of pathway activation on hypoxia-mediated downregulation of mTOR signaling, raising the possibility that rapalogs could selectively inhibit hypoxic cells.
journal_name
Cancer Celljournal_title
Cancer cellauthors
Easton JB,Kurmasheva RT,Houghton PJdoi
10.1016/j.ccr.2006.02.027keywords:
subject
Has Abstractpub_date
2006-03-01 00:00:00pages
153-5issue
3eissn
1535-6108issn
1878-3686pii
S1535-6108(06)00062-6journal_volume
9pub_type
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