Show simple item record

dc.contributor.advisorDwyer, Roisin
dc.contributor.authorRyan, James John
dc.date.accessioned2014-06-19T08:28:24Z
dc.date.available2014-06-19T08:28:24Z
dc.date.issued2014-05-07
dc.identifier.urihttp://hdl.handle.net/10379/4396
dc.description.abstractIntroduction: The Sodium Iodide Symporter (NIS) facilitates iodide accumulation in the thyroid and radioiodide imaging and treatment of thyroid disease. Studies have suggested that elevated levels of NIS expression in malignant breast tissue may facilitate diagnosis, imaging and treatment of breast cancer. Alternative approaches, such as Adenovirus-based NIS gene therapy is limited by vector immunogenicity and an inability to specifically target tumours. Mesenchymal Stem Cells (MSCs) may represent appropriate cellular vehicles as a result of their proven tumour tropism and immune privilege. The aim of this project was to determine the presence, relevance and regulation of native mammary NIS expression and to explore the potential of MSC -mediated NIS gene therapy of breast cancer. Methods: Expression of NIS, and putative regulators (Retinoic acid receptors (RAR), Estrogen receptor (ER), Phosphoinositide-3-kinase (PI3K), and Thyroid hormone receptors (THR)) were determined by Relative Quantitative-Polymerase Chain Reaction (RQ-PCR) in 100 breast tissue specimens that included 15 controls. In vitro the effects of individual and combined estradiol, retinoic acid (RA) and thyroxine stimulation on NIS expression was determined in breast cancer cell lines. MSCs were engineered to express NIS and characterised in terms of phenotype and persistence of NIS expression and function. The distribution of systemically injected MSC-NIS in non-invasive disease and labelled MSCs in metastatic murine breast cancer models was determined over time. Results: NIS gene expression levels were significantly higher in malignant tissue compared to normal but even higher in benign tissue. Significant positive correlations in gene expression suggested relationships between NIS and putative regulators: RAR[alpha], RAR[beta], ER[alpha] and THR[beta] which were confirmed by estradiol, RA and thyroxine stimulation of NIS expression in vitro. Combined stimulation with RA and thyroxine had a synergistic effect on NIS expression. MSCs were successfully engineered to express NIS with no significant impact on phenotype observed. A cytotoxic effect on adjacent breast cancer cells was also demonstrated using Iodide131 in vitro. In animal models, initial ectopic engraftment was shown to deplete over time except in malignant tissue and tumour-targeted MSC tropism as well as successful delivery of transgene to tumour sites was observed. Conclusion: This thesis presents novel data on the presence and relevance of mammary NIS expression in human tissues. It also supports a regulatory role for estradiol and retinoic acid, and introduces the potential for thyroid hormones to stimulate mammary NIS expression. The phenotype and migratory behaviour of labelled and Ad5/CMV/NIS infected MSCs demonstrated here strongly support the potential of MSC-mediated NIS gene therapy of breast canceren_US
dc.subjectBreast canceren_US
dc.subjectMesenchymal stem cellsen_US
dc.subjectGene therapyen_US
dc.subjectSodium iodide symporteren_US
dc.subjectNISen_US
dc.subjectThyroiden_US
dc.subjectSurgeryen_US
dc.subjectMathematicsen_US
dc.titleMeseanchymal stem cell mediated sodium iodide symporter gene therapy of breast canceren_US
dc.typeThesisen_US
dc.contributor.funderCancer Research Irelanden_US
dc.contributor.funderNational Breast Cancer Research Instituteen_US
dc.local.noteThe sodium iodide symporter (NIS) facilitates iodide uptake into cells. It is present at high levels in the thyroid and so can facilitate radioiodide treatment of thyroid disease including cancer. This thesis investigated the potential for NIS mediated radioiodide therapy in breast cancer. It examines the relevence and regulation of naturally expressed NIS in breast tissue and also looks at the potential for delivery of cells engineered to express high levels of NIS to malignant breast tissue and associated metastases.en_US
dc.local.finalYesen_US
nui.item.downloads452


Files in this item

Attribution-NonCommercial-NoDerivs 3.0 Ireland
This item is available under the Attribution-NonCommercial-NoDerivs 3.0 Ireland. No item may be reproduced for commercial purposes. Please refer to the publisher's URL where this is made available, or to notes contained in the item itself. Other terms may apply.

The following license files are associated with this item:

Thumbnail
Thumbnail
Thumbnail
Thumbnail

This item appears in the following Collection(s)

Show simple item record