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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
Jazyk angličtina Země Česko
NLK
Directory of Open Access Journals
od 2001
Free Medical Journals
od 1998
Medline Complete (EBSCOhost)
od 2007-06-01
ROAD: Directory of Open Access Scholarly Resources
od 2001
- MeSH
- čipová analýza tkání metody MeSH
- DNA-topoisomerasy typu II genetika imunologie izolace a purifikace MeSH
- exprese genu genetika imunologie MeSH
- financování organizované MeSH
- imunohistochemie metody využití MeSH
- medicína založená na důkazech MeSH
- modely u zvířat MeSH
- myši inbrední NOD MeSH
- myši SCID MeSH
- proteiny spojené s mnohočetnou rezistencí k lékům genetika imunologie izolace a purifikace MeSH
- vault ribonucleoprotein particles genetika imunologie izolace a purifikace MeSH
- Wilmsův nádor genetika imunologie MeSH
- xenogenní modely - testy protinádorové aktivity metody využití MeSH
- zvířata MeSH
- Check Tag
- zvířata 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.
Citace poskytuje Crossref.org
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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