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

Research output: Contribution to journalArticlepeer-review

10 Scopus citations

Abstract

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.

Original languageEnglish
Pages (from-to)386-394
Number of pages9
JournalCurrent Eye Research
Volume34
Issue number5
DOIs
StatePublished - May 2009

Bibliographical note

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.

Funding

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.

FundersFunder number
Research to Prevent Blindness
St. Giles Foundation

    Keywords

    • Chemotherapy
    • MRP-1/P-glycoprotein
    • Multi-drug resistance
    • Pregnane X receptor
    • Retinoblastoma

    ASJC Scopus subject areas

    • Ophthalmology
    • Sensory Systems
    • Cellular and Molecular Neuroscience

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