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Expression of multidrug resistance-related protein (MRP-1), lung resistance-related protein (LRP) and topoisomerase-II (TOPO-II) in Wilms' tumor: immunohistochemical study using TMA methodology
Eduard Fridman, Jozef Skarda, Jonatan H Pinthus, Jonathan Ramon, Yoran Mor
Language English Country Czech Republic
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- MeSH
- Tissue Array Analysis methods MeSH
- DNA Topoisomerases, Type II genetics immunology isolation & purification MeSH
- Gene Expression genetics immunology MeSH
- Financing, Organized MeSH
- Immunohistochemistry methods utilization MeSH
- Evidence-Based Medicine MeSH
- Models, Animal MeSH
- Mice, Inbred NOD MeSH
- Mice, SCID MeSH
- Multidrug Resistance-Associated Proteins genetics immunology isolation & purification MeSH
- Vault Ribonucleoprotein Particles genetics immunology isolation & purification MeSH
- Wilms Tumor genetics immunology MeSH
- Xenograft Model Antitumor Assays methods utilization MeSH
- Animals MeSH
- Check Tag
- Animals MeSH
microarrayAims: MRP-1, LRP and TOPO-II are all associated with protection of the cells from the adverse eff ects of variouschemotherapeutics. The aim of this study was to measure the expression of these proteins in Wilms' tumor (WT).Materials and Methods: TMA block was constructed from 14 samples of WT's and from xenografts derived fromthem. Sections of the TMA were used for immunostaining against MRP-1, LRP and TOPO-IIa.Results: All normal kidneys expressed MRP-1 but were either weakly or negatively stained for LRP and TOPO-IIa.In WT samples, MRP-1 was universally expressed, exclusively in the tubular component, while there was no expressionof LRP and TOPO-IIa showed heterogeneous distribution. The xenografts varied in their MRP-1 and TOPO-IIaexpression and exhibited weak/negative staining of LRP.Conclusions: This study shows that although all the proteins evaluated, had diff erent expression patterns in thetumor samples, the most prominent changes in expression were found for MRP-1. The exact clinical implications ofthese changes in expression and their relevance to the resistance of these tumors to chemotherapy requires furtherinvestigation. The fi nding of diff erent expression profi les for the multidrug resistance proteins in the original WT'sand their xenografts suggests that the results of animal cancer models may be diffi cult to interpret.
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Lit.: 21
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- $a Expression of multidrug resistance-related protein (MRP-1), lung resistance-related protein (LRP) and topoisomerase-II (TOPO-II) in Wilms' tumor: immunohistochemical study using TMA methodology / $c Eduard Fridman, Jozef Skarda, Jonatan H Pinthus, Jonathan Ramon, Yoran Mor
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- $a Departments of Pathology and Urology, Chaim Sheba Medical Center, Tel-Aviv University, Tel-Aviv
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- $a Lit.: 21
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- $a microarrayAims: MRP-1, LRP and TOPO-II are all associated with protection of the cells from the adverse eff ects of variouschemotherapeutics. The aim of this study was to measure the expression of these proteins in Wilms' tumor (WT).Materials and Methods: TMA block was constructed from 14 samples of WT's and from xenografts derived fromthem. Sections of the TMA were used for immunostaining against MRP-1, LRP and TOPO-IIa.Results: All normal kidneys expressed MRP-1 but were either weakly or negatively stained for LRP and TOPO-IIa.In WT samples, MRP-1 was universally expressed, exclusively in the tubular component, while there was no expressionof LRP and TOPO-IIa showed heterogeneous distribution. The xenografts varied in their MRP-1 and TOPO-IIaexpression and exhibited weak/negative staining of LRP.Conclusions: This study shows that although all the proteins evaluated, had diff erent expression patterns in thetumor samples, the most prominent changes in expression were found for MRP-1. The exact clinical implications ofthese changes in expression and their relevance to the resistance of these tumors to chemotherapy requires furtherinvestigation. The fi nding of diff erent expression profi les for the multidrug resistance proteins in the original WT'sand their xenografts suggests that the results of animal cancer models may be diffi cult to interpret.
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