Expression of the multi-drug resistance proteins and the pregnane X receptor in treated and untreated retinoblastoma

  • Matthew W. Wilson
  • , Charles H. Fraga
  • , Carlos Rodriguez-Galindo
  • , Nikolas Hagedorn
  • , Markos L. Leggas
  • , Clinton Stewart

Producción científica: Articlerevisión exhaustiva

11 Citas (Scopus)

Resumen

Purpose: To compare the expression of pregnane xenobiotic receptor and certain multi-drug resistance proteins in retinoblastoma. Methods: Using tissue microarray analyses, we studied 62 pathology specimens for expression of pregnane xenobiotic receptor, multi-drug resistance 1/P glycoprotein, multi-drug resistance proteins 1, 2, and 4, and breast cancer resistant protein. Results: Comparing tumors treated with primary enucleation with tumors treated with chemotherapy and/or radiation showed no significant differences in the expression of multi-drug resistance proteins or pregnane xenobiotic receptor. Pregnane xenobiotic receptor was correlated with multi-drug resistance protein 2 expression (p 0.001). Conclusion: Our results indicate selection, rather than induction, of chemoresistant cells as a cause for treatment failure in managing retinoblastoma with primary systemic chemotherapy.

Idioma originalEnglish
Páginas (desde-hasta)386-394
Número de páginas9
PublicaciónCurrent Eye Research
Volumen34
N.º5
DOI
EstadoPublished - may 2009

Nota bibliográfica

Funding Information:
This study was supported by grants to Matthew W. Wilson from Research to Prevent Blindness, Inc., New York, NY, and the St. Giles Foundation, New York, NY.

Financiación

This study was supported by grants to Matthew W. Wilson from Research to Prevent Blindness, Inc., New York, NY, and the St. Giles Foundation, New York, NY.

Financiadores
Research to Prevent Blindness
St. Giles Foundation

    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

    • Ophthalmology
    • Sensory Systems
    • Cellular and Molecular Neuroscience

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