Skip to main content

Part of UT Health San Antonio

Graduate School of Biomedical Sciences, UT Health San AntonioGraduate School of Biomedical Sciences, UT Health San Antonio

Part of UT Health San Antonio

Give
Search

Quicklinks

Commencement

  • Commencement 2021

Logins

  • Canvas
  • CourseLeaf
  • IMPACT
  • LiveMail
  • Syllabus Depot
  • My UT Health (Intranet)

Resources

  • COVID-19 Updates for Students
  • Enrolled Student Resources
  • Educational Resources
  • GSBS Data Request Form

 Close Quicklinks

 
Menu
  • About
  • Admissions
  • Programs
  • Research
  • Faculty
  • Student Life
  • Alumni

You are here

  • Faculty directory
  • Houghton, Peter
houghton_peter

Contact

210-562-9056

HoughtonP@uthscsa.edu

Programs

Cancer Biology
M.S. in Personalized Molecular Medicine
Ph.D. in Integrated Biomedical Sciences

Departments & Divisions

Department of Molecular Medicine
Department of Pediatrics

Institutes and Centers

  • Greehey Children’s Cancer Research Institute

Research

Researcher profile

Peter Houghton, Ph.D.

Professor

Principal Investigator

Developmental Therapeutics

Cancer Pharmacology/Drug development for pediatric solid tumors

The lab focuses on developing novel approaches to the treatment of childhood cancer, with funded projects on childhood sarcoma, low-grade glioma, and developing new in vivo models. Our research focuses on fundamental aspects of tumorigenesis, such as identifying proteins that interact with fusion oncogenes that are essential for tumor cell proliferation and survival, and on understanding proliferative signals that are required for proliferation and survival. For pediatric sarcoma, our focus is on growth factor signaling, and understanding the basis for intrinsic and acquired resistance to inhibitors of insulin-like growth factor signaling. Our studies of childhood glioma focus on tumors with mutated (activated) BRAF signaling and exploiting this defect to develop novel therapeutic approaches to prevent the development of drug resistance. A unifying theme running through all studies is the use of Patient-Derived Xenografts (PDX) where tumors from patients are engrafted into immune-incompetent mice. These models provide clinically relevant tissue to study biologic characteristics and to test new therapeutic approaches. The lab is a member of the Pediatric Preclinical Testing Consortium, supported by the NCI to evaluate novel therapeutics. The lab also has a major effort in developing and molecularly characterizing new PDX models of both leukemias and solid tumors from Hispanic patients in Texas.

Related diseases: Pediatric sarcomas (rhabdomyosarcoma, Ewing sarcoma), low-grade brain tumors (glioma), pediatric cancers of the kidney (atypical teratoid/rhabdoid), and nephroblastoma (Wilms tumor)

Techniques: Contemporary molecular biology techniques, patient-derived xenografts (PDX), single-cell sequencing, CyTOF, cell sorting, FACs, protein purification, mass spectrometry, cell culture. 

  • Research & Grants

    Research profile

  • Publications

    Singh M, Leasure JM, Chronowski C, Geier B, Bondra K, Duan W, Hensley LA, Villalona-Calero M, Li N, Vergis AM, Kurmasheva RT, Shen C, Woods G, Sebastian N, Fabian D, Kaplon R, Hammond S, Palanichamy K, Chakravarti A, Houghton PJ. FANCD2 is a potential therapeutic target and biomarker in alveolar rhabdomyosarcoma harboring the PAX3-FOXO1 fusion gene. doi: 10.1158/1078-0432.CCR-13-0556. Epub 2014 Apr 30.PMID: 24787670

    Cam M, Bid HK, Xiao L, Zambetti GP, Houghton PJ, Cam H. J. p53/TAp63 and AKT regulate mammalian target of rapamycin complex 1 (mTORC1) signaling through two independent parallel pathways in the presence of DNA damage. Biol Chem. 2014 Feb 14;289(7):4083-94. doi: 10.1074/jbc.M113.530303. Epub 2013 Dec 23.PMID: 24366874

    Bid HK, Roberts RD, Cam M, Audino A, Kurmasheva RT, Lin J, Houghton PJ, Cam H. ΔNp63 promotes pediatric neuroblastoma and osteosarcoma by regulating tumor angiogenesis. Cancer Res. 2014 Jan 1;74(1):320-9. doi: 10.1158/0008-5472.CAN-13-0894. Epub 2013 Oct 23.PMID: 24154873

    Balkhi MY, Iwenofu OH, Bakkar N, Ladner KJ, Chandler DS, Houghton PJ, London CA, Kraybill W, Perrotti D, Croce CM, Keller C, Guttridge DC. miR-29 acts as a decoy in sarcomas to protect the tumor suppressor A20 mRNA from degradation by HuR.Sci Signal. 2013 Jul 30;6(286):ra63. doi: 10.1126/scisignal.2004177. Erratum in: Sci Signal. 2013 Sep 10;6(292):er6. Balkhi, Mumtaz Y [corrected to Balkhi, M Y]. PMID: 23901138

    Shen C, Houghton PJ. The mTOR pathway negatively controls ATM by up-regulating miRNAs. Proc Natl Acad Sci U S A. 2013 Jul 16;110(29):11869-74. doi: 10.1073/pnas.1220898110. Epub 2013 Jul 1.PMID: 23818585

Map image of UT Health San Antonio location
UT Health San Antonio
Graduate School of Biomedical Sciences

7703 Floyd Curl Drive

San Antonio, TX 78229

210-567-3709

gsbs@uthscsa.edu

  • About us
  • Contact us
  • Maps & directions

We make lives better ®

The University of Texas Health Science Center at San Antonio, also called UT Health San Antonio, is a leading academic health center with a mission to make lives better through excellence in advanced academics, life-saving research and comprehensive clinical care including health, dental and cancer services.

Web Privacy | Links from websites affiliated with UT Health's website (uthscsa.edu) to other websites do not constitute or imply university endorsement of those sites, their content, or products and services associated with those sites. The content on this website is intended to be used for informational purposes only. Health information on this site is not meant to be used to diagnose or treat conditions. Consult a health care provider if you are in need of treatment.