Literature DB >> 16530700

IRS-1: auditing the effectiveness of mTOR inhibitors.

John B Easton1, Raushan T Kurmasheva, Peter J Houghton.   

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.

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Year:  2006        PMID: 16530700     DOI: 10.1016/j.ccr.2006.02.027

Source DB:  PubMed          Journal:  Cancer Cell        ISSN: 1535-6108            Impact factor:   31.743


  29 in total

1.  Identification of optimal drug combinations targeting cellular networks: integrating phospho-proteomics and computational network analysis.

Authors:  Sergio Iadevaia; Yiling Lu; Fabiana C Morales; Gordon B Mills; Prahlad T Ram
Journal:  Cancer Res       Date:  2010-07-19       Impact factor: 12.701

Review 2.  Everolimus.

Authors:  Peter J Houghton
Journal:  Clin Cancer Res       Date:  2010-02-23       Impact factor: 12.531

Review 3.  mTOR-targeted cancer therapy: great target but disappointing clinical outcomes, why?

Authors:  Shi-Yong Sun
Journal:  Front Med       Date:  2020-11-09       Impact factor: 4.592

4.  Intrinsically lower AKT, mammalian target of rapamycin, and hypoxia-inducible factor activity correlates with increased sensitivity to 2-deoxy-D-glucose under hypoxia in lung cancer cell lines.

Authors:  Medhi Wangpaichitr; Niramol Savaraj; Johnathan Maher; Metin Kurtoglu; Theodore J Lampidis
Journal:  Mol Cancer Ther       Date:  2008-06       Impact factor: 6.261

Review 5.  Mammalian target of rapamycin inhibition as a therapeutic strategy in the management of urologic malignancies.

Authors:  Jorge A Garcia; David Danielpour
Journal:  Mol Cancer Ther       Date:  2008-06       Impact factor: 6.261

6.  The prolyl peptidases PRCP/PREP regulate IRS-1 stability critical for rapamycin-induced feedback activation of PI3K and AKT.

Authors:  Lei Duan; Guoguang Ying; Brian Danzer; Ricardo E Perez; Zia Shariat-Madar; Victor V Levenson; Carl G Maki
Journal:  J Biol Chem       Date:  2014-06-16       Impact factor: 5.157

7.  IRS1 regulation by Wnt/beta-catenin signaling and varied contribution of IRS1 to the neoplastic phenotype.

Authors:  Guido T Bommer; Ying Feng; Ayaka Iura; Thomas J Giordano; Rork Kuick; Hüseyin Kadikoy; Deanna Sikorski; Rong Wu; Kathleen R Cho; Eric R Fearon
Journal:  J Biol Chem       Date:  2009-10-20       Impact factor: 5.157

8.  Dual inhibition of PI3Kalpha and mTOR as an alternative treatment for Kaposi's sarcoma.

Authors:  Risa Chaisuparat; Jiadi Hu; Bruno C Jham; Zachary A Knight; Kevan M Shokat; Silvia Montaner
Journal:  Cancer Res       Date:  2008-10-15       Impact factor: 12.701

Review 9.  Enhancing mTOR-targeted cancer therapy.

Authors:  Xuerong Wang; Shi-Yong Sun
Journal:  Expert Opin Ther Targets       Date:  2009-10       Impact factor: 6.902

Review 10.  mTOR signalling in human cancer.

Authors:  J Albanell; A Dalmases; A Rovira; F Rojo
Journal:  Clin Transl Oncol       Date:  2007-08       Impact factor: 3.405

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