Cited by 180

The DOI matches its Crossref record; 7 of the 7 references it cites were found in a registry or an index.

A Kinase Inhibitor Targeted to mTORC1 Drives Regression in Glioblastoma

Fan, QiWen, Aksoy, Ozlem, Wong, Robyn A., Ilkhanizadeh, Shirin, Novotny, Chris J., Gustafson, William C., Truong, Albert Yi-Que, Cayanan, Geraldine, Simonds, Erin F., Haas-Kogan, Daphne, Phillips, Joanna J., Nicolaides, Theodore, Okaniwa, Masanori, Shokat, Kevan M., Weiss, William A.·2017·Cancer Cell

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Crossref · 10.1016/j.ccell.2017.01.014

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Research works printed but not linked: 21

  1. Baretić, 2014, The structural basis for mTOR function, Semin. Cell Dev. Biol., 36, 91, 10.1016/j.semcdb.2014.09.024 · DOI
  2. Bradshaw, 2015, Prolonged and tunable residence time using reversible covalent kinase inhibitors, Nat. Chem. Biol., 11, 525, 10.1038/nchembio.1817 · DOI
  3. Choi, 1996, Structure of the FKBP12-rapamycin complex interacting with the binding domain of human FRAP, Science, 273, 239, 10.1126/science.273.5272.239 · DOI
  4. Fan, 2006, A dual PI3 kinase/mTOR inhibitor reveals emergent efficacy in glioma, Cancer Cell, 9, 341, 10.1016/j.ccr.2006.03.029 · DOI
  5. Fan, 2007, A dual phosphoinositide-3-kinase {alpha}/mTOR inhibitor cooperates with blockade of epidermal growth factor receptor in PTEN-mutant glioma, Cancer Res., 67, 7960, 10.1158/0008-5472.CAN-07-2154 · DOI
  6. Fan, 2009, EGFR signals to mTOR through PKC and independently of Akt in glioma, Sci. Signal, 2, ra4, 10.1126/scisignal.2000014 · DOI
  7. Feldman, 2009, Active-site inhibitors of mTOR target rapamycin-resistant outputs of mTORC1 and mTORC2, PLoS Biol., 7, e38, 10.1371/journal.pbio.1000038 · DOI
  8. Folkes, 2008, The identification of 2-(1H-indazol-4-yl)-6-(4-methanesulfonyl-piperazin-1-ylmethyl)-4-morpholin-4-yl-thieno[3,2-d]pyrimidine (GDC-0941) as a potent, selective, orally bioavailable inhibitor of class I PI3 kinase for the treatment of cancer, J. Med. Chem., 51, 5522, 10.1021/jm800295d · DOI
  9. Garcia-Martinez, 2009, Ku-0063794 is a specific inhibitor of the mammalian target of rapamycin (mTOR), Biochem. J., 421, 29, 10.1042/BJ20090489 · DOI
  10. Gaubitz, 2015, Molecular basis of the rapamycin insensitivity of target of rapamycin complex 2, Mol. Cell, 58, 977, 10.1016/j.molcel.2015.04.031 · DOI · Paper page
  11. Hirai, 2010, MK-2206, an allosteric Akt inhibitor, enhances antitumor efficacy by standard chemotherapeutic agents or molecular targeted drugs in vitro and in vivo, Mol. Cancer Ther., 9, 1956, 10.1158/1535-7163.MCT-09-1012 · DOI
  12. Houghton, 2010, Stage 2 combination testing of rapamycin with cytotoxic agents by the Pediatric Preclinical Testing Program, Mol. Cancer Ther., 9, 101, 10.1158/1535-7163.MCT-09-0952 · DOI
  13. Ilagan, 2016, Emerging role of mTOR in the response to cancer therapeutics, Trends Cancer, 2, 241, 10.1016/j.trecan.2016.03.008 · DOI
  14. MacMillan, 2013, FK506 binding proteins: cellular regulators of intracellular Ca2+ signalling, Eur. J. Pharmacol., 700, 181, 10.1016/j.ejphar.2012.12.029 · DOI
  15. Nagane, 1998, Drug resistance of human glioblastoma cells conferred by a tumor-specific mutant epidermal growth factor receptor through modulation of Bcl-XL and caspase-3-like proteases, Proc. Natl. Acad. Sci. USA, 95, 5724, 10.1073/pnas.95.10.5724 · DOI
  16. Omuro, 2013, Glioblastoma and other malignant gliomas: a clinical review, JAMA, 310, 1842, 10.1001/jama.2013.280319 · DOI
  17. Sarkaria, 2006, Use of an orthotopic xenograft model for assessing the effect of epidermal growth factor receptor amplification on glioblastoma radiation response, Clin. Cancer Res., 12, 2264, 10.1158/1078-0432.CCR-05-2510 · DOI · Paper page
  18. Sato, 2010, Single amino-acid changes that confer constitutive activation of mTOR are discovered in human cancer, Oncogene, 29, 2746, 10.1038/onc.2010.28 · DOI
  19. Sun, 2005, Activation of Akt and eIF4E survival pathways by rapamycin-mediated mammalian target of rapamycin inhibition, Cancer Res., 65, 7052, 10.1158/0008-5472.CAN-05-0917 · DOI
  20. Swartling, 2010, Pleiotropic role for MYCN in medulloblastoma, Genes Dev., 24, 1059, 10.1101/gad.1907510 · DOI
  21. Taylor, 2012, Targeting EGFR for treatment of glioblastoma: molecular basis to overcome resistance, Curr. Cancer Drug Targets, 12, 197, 10.2174/156800912799277557 · DOI

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Metadata

Authors
Fan, Q., Aksoy, O., Wong, R. A., Ilkhanizadeh, S., Novotny, C. J., Gustafson, W. C., Truong, A. Y.-Q., Cayanan, G., Simonds, E. F., Haas-Kogan, D., Phillips, J. J., Nicolaides, T., Okaniwa, M., Shokat, K. M., & Weiss, W. A.
Venue
Cancer Cell
Publisher
Elsevier BV
Published
2017-03
Volume
31
Issue
3
Pages
424-435
ISSN
1535-6108
Cited by
180
References
7
Language
en
Funders
  • NIH (R01NS091620, R01NS089868, R01CA148699, U01CA176287, P30CA82103, U54CA163155, P50AA017072)
  • Kura Oncology
  • Children’s Tumor
  • CureSearch
  • Ross K. MacNeill
  • Samuel Waxman Cancer Research Foundations

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