Research Topics
| Peter HoughtonSummaryAffiliation: Nationwide Children's Hospital Country: USA Publications
Research Grants
| Collaborators
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Detail Information
Publications
Potent inhibition of angiogenesis by the IGF-1 receptor-targeting antibody SCH717454 is reversed by IGF-2Hemant K Bid
Center for Childhood Cancer, The Research Institute, Nationwide Children s Hospital, 700 Children s Drive, Columbus, OH 43205, USA
Mol Cancer Ther 11:649-59. 2012..Many childhood cancers secrete IGF-2, suggesting that tumor-derived IGF-2 in the microenvironment maintains angiogenesis in the presence of IGF-1R-targeted antibodies allowing tumor progression...
Initial testing (stage 1) of LCL161, a SMAC mimetic, by the Pediatric Preclinical Testing ProgramPeter J Houghton
Nationwide Children s Hospital, Columbus, Ohio 43205, USA
Pediatr Blood Cancer 58:636-9. 2012..No objective tumor responses were observed. In vivo LCL161 demonstrated limited single agent activity against the pediatric preclinical models studied...
Stage 2 combination testing of rapamycin with cytotoxic agents by the Pediatric Preclinical Testing ProgramPeter J Houghton
Center for Children s Cancer, Nationwide Children s Hospital, Columbus, Ohio 43205, USA
Mol Cancer Ther 9:101-12. 2010....
EverolimusPeter J Houghton
Center for Childhood Cancer, The Research Institute, Nationwide Children s Hospital, Columbus, Ohio 43205, USA
Clin Cancer Res 16:1368-72. 2010..Further, biomarkers that predict tumor sensitivity are still elusive. The mechanism of action, preclinical antitumor activity, and clinical activity of everolimus against RCC are reviewed...
Initial testing (stage 1) of the mTOR kinase inhibitor AZD8055 by the pediatric preclinical testing programPeter J Houghton
Nationwide Children s Hospital, Columbus, OH, USA
Pediatr Blood Cancer 58:191-9. 2012..Procedures AZD8055 was tested against the PPTP in vitro panel at concentrations ranging from 1.0 nM to 10 µM and against the PPTP in vivo panels at a dose of 20 mg/kg administered orally daily x 7 for 4 weeks...
Testing of the topoisomerase 1 inhibitor Genz-644282 by the pediatric preclinical testing programPeter J Houghton
Nationwide Children s Hospital, Columbus, OH, USA
Pediatr Blood Cancer 58:200-9. 2012..Genz-644282 is a novel non-camptothecin topoisomerase I poison that is in clinical development...
Initial testing of the hypoxia-activated prodrug PR-104 by the pediatric preclinical testing programPeter J Houghton
Nationwide Children s Hospital, Columbus, OH, USA
Pediatr Blood Cancer 57:443-53. 2011..PR-104 activation can occur via hypoxia-dependent reductases and also independently of hypoxia by aldo-keto reductase (AKR) 1C3...
Small molecules, LLL12 and FLLL32, inhibit STAT3 and exhibit potent growth suppressive activity in osteosarcoma cells and tumor growth in miceGrace Ifeyinwa Onimoe
Center for Childhood Cancer, The Research Institute at Nationwide Children s Hospital, Columbus, OH, USA
Invest New Drugs 30:916-26. 2012..Blocking persistent STAT3 signaling by LLL12 and FLLL32 may be a novel therapeutic approach for osteosarcoma...
mTORC1 signaling under hypoxic conditions is controlled by ATM-dependent phosphorylation of HIF-1αHakan Cam
Center for Childhood Cancer, Nationwide Children s Hospital, Columbus, OH 43205, USA
Mol Cell 40:509-20. 2010..Deregulation of these pathways in pediatric solid tumor xenografts suggests a link between mTORC1 dysregulation and solid tumor development and points to an important role for hypoxic regulation of mTORC1 activity in tumor development...
Research Grants
- Rapamycin-induced Selective Apoptosis in Malignant CellsPeter J Houghton; Fiscal Year: 2010..The studies have the potential to radically alter outcome for these children, and reduce the debilitating sequellae of high dose radiation and chemotherapy. ..
- Rapamycin-induced Selective Apoptosis in Malignant CellsPeter Houghton; Fiscal Year: 2009..The studies have the potential to radically alter outcome for these children, and reduce the debilitating sequellae of high dose radiation and chemotherapy. ..
- Rapamycin-induced Selective Apoptosis in Malignant CellsPeter Houghton; Fiscal Year: 2007..e. p53 or p21Cip1. Our studies will develop the biochemical framework to underpin a novel approach by which rapamycins can induce tumor-selective cytotoxicity based on the loss of the tumor suppressor p53. ..
- MTOR as a Therapeutic Target in Childhood CancerPeter Houghton; Fiscal Year: 2005..abstract_text> ..
- RAPAMYCIN INDUCED SELECTIVE APOPTOSIS IN MALIGNANT CELLSPeter Houghton; Fiscal Year: 2002..The long-term goal of these studies is to develop alternative curative therapy for children with cancer that will avoid the often devastating events, associated with contemporary intensive chemo-radiotherapy regimens. ..
