Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.567516
Title: The role of gamma-synuclein in mammary gland tumourigenesis
Author: Sharfeddin, Essam
Awarding Body: Cardiff University
Current Institution: Cardiff University
Date of Award: 2012
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Abstract:
Abstract y-synuclein is the third and last discovered member of the synuclein family, it is expressed mostly in the nervous system and its physiological function is still unknown. y-synuclein has been claimed to play a role in mammary gland tumourigenesis as its overexpression in cancer cells was shown to inhibit apoptosis and stimulate growth, proliferation, survival, motility and metastasis. However, the role of endogenous y-synuclein in mammary gland tumourigenesis has not been studied in an appropriate in vivo model. The results obtained in this study show that y-synuclein is not required for the normal development of the mammary gland at any developmental stage - embryonic, pubertal or reproductive. Furthermore, ablation of y-synuclein did not prevent induction of mammary gland tumours by activated ErbB2 transgene in mammary gland epithelium. Unexpectedly, transgenic activated ErbB2 hemizygous, y-synuclein knockout female mice developed slightly more tumours with a significantly shorter tumour latency than the wild type littermates. These animals also exhibited similar tumour growth rates and metastases to the lungs, and a slightly shorter survival. Overall, a trend for accelerated tumourigenesis in the absence of y-synuclein was observed. Thus, it is feasible that the aberrant expression of y-synuclein reported in advance-stage tumours and metastases reflects activation of pathways aimed at repressing rather than enhancing tumourigenesis, as widely thought. Future studies will clarify the role of y-synuclein in ErbB2-induced mammary gland tumourigenesis.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.567516  DOI: Not available
Keywords: QP Physiology
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