Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.683595
Title: Changes in cellular phenotype and resistance to cisplatin in an oral squamous carcinoma model over-expressing cytoglobin
Author: Thorne, Lorna Susan
ISNI:       0000 0004 5917 2405
Awarding Body: University of Birmingham
Current Institution: University of Birmingham
Date of Award: 2016
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Abstract:
Although cytoglobin is widely considered a tumour suppressor, re-expression plays a role in disease progression in a subset of oral squamous cell carcinomas (OSC), but the mechanism of action is not understood. In this thesis, we developed a new OSC cell model to study the effects of cytoglobin over­ expression on cellular phenotype and resistance to cisplatin. Microarray analysis of cytoglobin­ expressing cells showed significantly altered transcripts related to stress response, adhesion and locomotion, and metabolism. Treatment of cytoglobin-expressing cells with cisplatin revealed a greater response in p53-regulated target expression (MAP3K5, NQOl, CDKN2A and GADD45A) compared to non-expressing cells. Further investigation showed this was associated with higher CHKl, p53 and p21 protein levels, suggesting enhanced activation of p53 signalling pathways. Furthermore, cytoglobin-expressing cells were more resistant to cisplatin-induced apoptosis and altered their cell cycle distribution. These changes were linked to reduced total cellular and mitochondrial superoxide. Collectively, these findings demonstrate for the first time that cytoglobin over- expression is associated with resistance to cisplatin-induced cytotoxicity and the mechanism involves p53 signalling. In conclusion, we propose expression of cytoglobin may afford tumours cells a survival advantage in the harsh environmental conditions of the developing tumour as well as resistance to drugs like cisplatin.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.683595  DOI: Not available
Keywords: QR Microbiology
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