Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.712825
Title: The role of microRNA-515-5p in breast cancer
Author: Pinho, Filipa Gomes
Awarding Body: Imperial College London
Current Institution: Imperial College London
Date of Award: 2014
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Abstract:
MicroRNAs are a class of small non-coding RNAs which modulate a wide range of physiological and pathological processes by negatively regulating gene expression at the post-transcriptional level. MicroRNAs have been found to be important modulators of the tumorigenesis and metastasis formation of different human cancers, including breast cancer. Here we prove that miR-515-5p belongs to a particular subset of microRNAs which mediate estradiol (E2) action in the carcinogenesis of estrogen receptor-positive breast cancers, in which proliferation is highly dependent on E2. We show that miR-515-5p downregulation is the main responsible for the positive effect of E2 in the expression of SK1, an oncogenic enzyme required for E2-dependent breast cancer tumorigenesis. Upon E2 stimulation, estrogen receptor α (ERα) directly represses the transcription of miR-515-5p which leads to the upregulation of SK1 expression as a result of its reduced availability to target SK1. By conducting the first functional studies of miR-515-5p, here we also demonstrate that miR-515-5p plays a tumour suppressive role in breast cancer. miR-515-5p was found to inhibit breast cancer proliferation by inducing caspase-dependent apoptosis via SK1 and to repress breast cancer cell motility mainly by targeting MARK4, an enzyme implicated in the regulation of cell cytoskeleton dynamics. Overall, we identify a new signaling pathway involving ERα, SK1 and miR-515-5p and a new role for miR-515-5p which highlights its therapeutic potential for the treatment of breast cancer.
Supervisor: Stebbing, Justin ; Castellano, Leandro Sponsor: Fundacao para a Ciencia e a Tecnologia
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.712825  DOI: Not available
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