Immunohistochemical detection of multidrug-resistant protein expression in retinoblastoma treated by primary enucleation

  • Matthew W. Wilson
  • , Charles H. Fraga
  • , Christine E. Fuller
  • , Carlos Rodriguez-Galindo
  • , John Mancini
  • , Nikolaus Hagedorn
  • , Markos L. Leggas
  • , Clinton F. Stewart

Producción científica: Articlerevisión exhaustiva

32 Citas (Scopus)

Resumen

PURPOSE. To compare the expression of multidrug-resistant proteins in retinoblastoma tumors among eyes treated with primary enucleation. METHODS. A group of 18 patients with unilateral retinoblastoma with advanced intraocular disease was selected for the study. All patients had undergone primary enucleation. A histologic specimen from each patient was retrieved from the pathology archives and a tissue gene microarray was constructed (0.6 x 3-4 mm). Standard immunohistochemical techniques were used to study the tissue microarrays for the expression of the ATP-binding cassette (ABC) transporters: breast cancer resistance protein (BCRP; ABCG2), multidrug-resistant protein 1/Pglycoprotein (MDR1/Pgp; ABCB1), multidrug-resistant-associated protein 1 (MRP1; ABCC1), MRP2 (ABCC2), and MRP4 (ABCC4). RESULTS. Of the 18 specimens retrieved, 16 had adequate tissue for study. MRP1 was expressed in 8 (50%) of 16 tumors, and MRP2 was expressed in 5 (31%) of 16 tumors. MDR1/Pgp was found in 2 (12%) of 16 retinoblastomas. MRP4 and BCRP were not detected in any of the tumors studied. CONCLUSIONS. The results show that multiple ABC transporters were present in a cohort of sporadic patients with unilateral retinoblastoma who underwent primary enucleation. Studies are planned of the expression of ABC transporters in eyes treated by chemotherapy and/or radiation as a comparison with this group.

Idioma originalEnglish
Páginas (desde-hasta)1269-1273
Número de páginas5
PublicaciónInvestigative Ophthalmology and Visual Science
Volumen47
N.º4
DOI
EstadoPublished - abr 2006

ASJC Scopus subject areas

  • Ophthalmology
  • Sensory Systems
  • Cellular and Molecular Neuroscience

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