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TRAIL gene therapy: From preclinical development to clinical application

  • Thomas S. Griffith
  • , Brittany Stokes
  • , Tamara A. Kucaba
  • , James K. Earel
  • , Rebecca L. VanOosten
  • , Erik L. Brinks
  • , Lyse A. Norian

Producción científica: Review articlerevisión exhaustiva

87 Citas (Scopus)

Resumen

Numerous studies have investigated the potential use of TNF-related apoptosis-inducing ligand (TRAIL) as a cancer therapeutic since its discovery in 1995 - because TRAIL is a potent inducer of apoptosis in tumor cells but not in normal cells and tissues. Consequently, a great deal is known about TRAIL/TRAIL receptor expression, the molecular components of TRAIL receptor signaling, and methods of altering tumor cell sensitivity to TRAIL-induced apoptosis. Our laboratory was the first to report the possibility of TRAIL gene transfer therapy as an alternative method of using TRAIL as an antitumor therapy. As with recombinant proteins administered systemically, intratumoral TRAIL gene delivery also has limitations that can restrict its full potential. Translating the preclinical TRAIL studies into the clinic has started, with the hope that TRAIL will exhibit robust tumoricidal activity against human primary tumors in situ with minimal toxic side effects.

Idioma originalEnglish
Páginas (desde-hasta)9-19
Número de páginas11
PublicaciónCurrent Gene Therapy
Volumen9
N.º1
DOI
EstadoPublished - 2009

Financiación

FinanciadoresNúmero del financiador
National Childhood Cancer Registry – National Cancer InstituteR01CA109446

    ODS de las Naciones Unidas

    Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible

    1. Good health and well being
      Good health and well being

    ASJC Scopus subject areas

    • Molecular Medicine
    • Molecular Biology
    • Genetics
    • Drug Discovery
    • Genetics(clinical)

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