Please use this identifier to cite or link to this item: http://hdl.handle.net/2381/28305
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dc.contributor.advisorTulchinsky, Eugene-
dc.contributor.advisorPringle, James-
dc.contributor.authorHill, Louise Anne-
dc.date.accessioned2013-10-17T12:02:09Z-
dc.date.available2013-10-17T12:02:09Z-
dc.date.issued2013-05-01-
dc.identifier.urihttp://hdl.handle.net/2381/28305-
dc.description.abstractThe master-regulators of an epithelial-mesenchymal transition (MR-EMT) have a pivotal role in the regulation of carcinoma development, promoting transformation and generating a migratory and invasive phenotype. Within epithelial cells, the ZEB proteins are co-regulated, jointly repressed by the miR-200 family of microRNAs. However, here it is demonstrated that the expression and regulation of the MR-EMT in malignant melanoma cell lines appears to be fundamentally different, with a hierarchical organisation identified. ZEB2 and SNAIL2 were found to be expressed in melanocytes, whilst ZEB1 and TWIST1 expression was acquired by a sub-set of malignant melanoma cell lines. Melanoma-initiating mutations within B-RAF and NRAS were shown to reversibly promote expression of ZEB1 and TWIST1 at the expense of ZEB2 and SNAIL2. Additionally, ZEB2 and SNAIL2 were identified up-stream of ZEB1 and TWIST1 within the MAPK signalling cascade, with ZEB2 functioning as a repressor of ZEB1. Furthermore, ZEB2 and SNAIL2 were found to positively regulate expression of MITF, a marker of melanocyte differentiation. In contrast, ZEB1 repressed expression of MITF and was the primary transcriptional repressor of E-cadherin, an adhesion molecule vital for the interaction between differentiated melanocytes and keratinocytes. Previously, within epithelial cell lines, all the MR-EMT have been identified as transcriptional repressors of E-cadherin. However, ZEB2 and SNAIL2 were co-expressed with E-cadherin within melanocytes and melanoma cell lines and, along with TWIST1, were not able to independently induce E-cadherin re-activation following repression. Surprisingly, ZEB2 became a repressor of E-cadherin in conjunction with ZEB1. Finally, E-cadherin expression was also shown to be controlled in a ZEB1-dependent manner by the transcriptional co-repressor BRG1, the ATPase subunit of the SWI/SNF chromatin remodelling complex, and by the presence of DNA methylation at the E-cadherin promoter. Indeed, DNA methylation was identified as a possible factor controlling the success rate of metastatic colonisation in melanoma cells, allowing for the dynamic re-expression of E-cadherin at the secondary site. These data demonstrate that in malignant melanoma the expression and regulation of the MREMT is fundamentally different to that of epithelial tumours, with the MR-EMT structured hierarchically, with opposing regulatory functions.en
dc.language.isoenen
dc.rightsCopyright © the author. All rights reserved.en
dc.subjectEMTen
dc.subjectCanceren
dc.subjectMelanomaen
dc.titleThe master-regulators of EMT and E-cadherin constitute a novel pathway in malignant melanomaen
dc.typeThesisen
dc.type.qualificationlevelDoctoralen
dc.type.qualificationnamePhDen
dc.date.award2013-05-01-
dc.publisher.institutionUniversity of Leicesteren_GB
Appears in Collections:Theses, Dept. of Cancer Studies & Molecular Medicine
Leicester Theses

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