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Modulators of MRP1 promoter in Neuroblastoma cell lines

The long term goal of this research proposal is to further understand the transcriptional regulation of the MRP1 promoter in neuroblastoma cells. We are primarily focused on two possible mechanisms that might lead to the regulation of MRP1 expression: epigenetic modifications, in particular, gene pr...

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Main Author: Ghabriel, Myret Said
Format: Thesis
Published: AUC Knowledge Fountain 2014
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access_status_str Open Access
author Ghabriel, Myret Said
author_browse Ghabriel, Myret Said
author_facet Ghabriel, Myret Said
author_sort Ghabriel, Myret Said
collection Thesis
dc_rights_str_mv The author retains all rights with regard to copyright. The author certifies that written permission from the owner(s) of third-party copyrighted matter included in the thesis, dissertation, paper, or record of study has been obtained. The author further certifies that IRB approval has been obtained for this thesis, or that IRB approval is not necessary for this thesis. Insofar as this thesis, dissertation, paper, or record of study is an educational record as defined in the Family Educational Rights and Privacy Act (FERPA) (20 USC 1232g), the author has granted consent to disclosure of it to anyone who requests a copy.
description The long term goal of this research proposal is to further understand the transcriptional regulation of the MRP1 promoter in neuroblastoma cells. We are primarily focused on two possible mechanisms that might lead to the regulation of MRP1 expression: epigenetic modifications, in particular, gene promoter methylation and transcription factors namely the regulation by the methyl binding protein (MeCP2). Within the 5’ untranslated region of the MRP1 promoter is a CpG island that has the potential to be methylated, thus contributing to down regulation of MRP1 expression in drug sensitive neuroblastoma cells. Our goal is to determine if methylation status of the promoter region and subsequently the recruitment of MeCP2 that may play a role in the regulation of MRP1 expression. The methylation status of the promoter will be investigated using Methylation specific PCR and Bisulfite sequencing; while MeCP2 binding will be examined using Chromatin Immunoprecipitation.This project addresses a very important question, which is why neuroblastoma patients develop drug resistance. Identifying regulatory mechanisms for MRP1 expression can potentially help us to determine prognostic factors for drug resistance and further down the road lead to the development of better treatment strategies.
format Thesis
id oai:fount.aucegypt.edu:etds-2172
institution American University in Cairo (Egypt)
last_indexed 2026-06-10T12:35:47.730Z
license_str Other — see source repository
provenance_str_mv Harvested via OAI-PMH from AUC Knowledge Fountain — bepress
publishDate 2014
publishDateRange 2014
publishDateSort 2014
publisher AUC Knowledge Fountain
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source_str AUC Knowledge Fountain — bepress
spelling oai:fount.aucegypt.edu:etds-2172 Modulators of MRP1 promoter in Neuroblastoma cell lines Ghabriel, Myret Said The long term goal of this research proposal is to further understand the transcriptional regulation of the MRP1 promoter in neuroblastoma cells. We are primarily focused on two possible mechanisms that might lead to the regulation of MRP1 expression: epigenetic modifications, in particular, gene promoter methylation and transcription factors namely the regulation by the methyl binding protein (MeCP2). Within the 5’ untranslated region of the MRP1 promoter is a CpG island that has the potential to be methylated, thus contributing to down regulation of MRP1 expression in drug sensitive neuroblastoma cells. Our goal is to determine if methylation status of the promoter region and subsequently the recruitment of MeCP2 that may play a role in the regulation of MRP1 expression. The methylation status of the promoter will be investigated using Methylation specific PCR and Bisulfite sequencing; while MeCP2 binding will be examined using Chromatin Immunoprecipitation.This project addresses a very important question, which is why neuroblastoma patients develop drug resistance. Identifying regulatory mechanisms for MRP1 expression can potentially help us to determine prognostic factors for drug resistance and further down the road lead to the development of better treatment strategies. 2014-02-01T08:00:00Z thesis application/pdf https://fount.aucegypt.edu/etds/1173 https://fount.aucegypt.edu/context/etds/article/2172/viewcontent/Modulators_20of_20MRP1_20promoter_20in_20Neuroblastoma_20cell_20lines_1.docx.pdf The author retains all rights with regard to copyright. The author certifies that written permission from the owner(s) of third-party copyrighted matter included in the thesis, dissertation, paper, or record of study has been obtained. The author further certifies that IRB approval has been obtained for this thesis, or that IRB approval is not necessary for this thesis. Insofar as this thesis, dissertation, paper, or record of study is an educational record as defined in the Family Educational Rights and Privacy Act (FERPA) (20 USC 1232g), the author has granted consent to disclosure of it to anyone who requests a copy. Theses and Dissertations AUC Knowledge Fountain Neuroblastoma Manufacturing resource planning
spellingShingle Neuroblastoma
Manufacturing resource planning
Ghabriel, Myret Said
Modulators of MRP1 promoter in Neuroblastoma cell lines
title Modulators of MRP1 promoter in Neuroblastoma cell lines
title_full Modulators of MRP1 promoter in Neuroblastoma cell lines
title_fullStr Modulators of MRP1 promoter in Neuroblastoma cell lines
title_full_unstemmed Modulators of MRP1 promoter in Neuroblastoma cell lines
title_short Modulators of MRP1 promoter in Neuroblastoma cell lines
title_sort modulators of mrp1 promoter in neuroblastoma cell lines
topic Neuroblastoma
Manufacturing resource planning
url https://fount.aucegypt.edu/etds/1173
https://fount.aucegypt.edu/context/etds/article/2172/viewcontent/Modulators_20of_20MRP1_20promoter_20in_20Neuroblastoma_20cell_20lines_1.docx.pdf
work_keys_str_mv AT ghabrielmyretsaid modulatorsofmrp1promoterinneuroblastomacelllines