Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.538362
Title: Systematic analysis of genomic alterations in prostate cancer
Author: Mao, Xueying
Awarding Body: Queen Mary, University of London
Current Institution: Queen Mary, University of London
Date of Award: 2011
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Abstract:
Prostate cancer is the most common male cancer in Western countries. The genetic mechanism underlying its initiation and progression is still unclear. The aim of this project was to identify novel genomic changes in prostate cancer and the underlying genetic mechanisms of prostate carcinogenesis using a high-resolution genome-wide analysis approach. Firstly, three prostate cancer cell lines, thirty-two UK and thirty-nine Chinese prostate cancer clinical samples were analysed using Affymetrix’s SNP microarrays (500K and array 6.0). Most of the common genomic changes observed in these samples are the same as those found in previous studies. Among the common genomic alterations, ERG rearrangements were also detected in 6/10 circulating tumour cell samples by flouroscence in situ hybridisation (FISH). Interestingly, loss of 21q22 and PTEN deletion, which were commonly found in Western prostate cancer, were rarely detected in the Chinese samples. This was further evaluated and comfirmed by FISH and immunohistochemistry analyses on UK and Chinese prostate cancer tissue microarrays and reverse transcript polymerase chain reaction (RT-PCR) analysis of TMPRSS2:ERG fusion transcripts in 48 UK and 66 Chinese fresh frozen cases (p<0.001). Subsequently, I identified a difference in the AR CAG repeat length polymorphism between UK and Chinese samples. This genetic disparity indicates differential distribution of causative/protective factors in these two populations. To study chromosome rearrangements and fusion genes, I developed a high-resolution karyotype approach to fully karyotype three cell lines, and identified five potential genomic fusions. Genomic fusion sequence of MAMDC1:SCL25A21 was identified, but the expected fusion transcript could not be detected by RT-PCR. As metaphase spreads are difficult to make in prostate cancer clinical samples, I used a common breakpoint identification approach and identified many frequently truncated genes. During this study, I observed extensive intratumour heterogeneity, which reflects genomic instability in prostate cancer. Therefore, I investigated the involvement of genomic instability in human cancers through genomic analysis of four 2N cancer cell lines.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.538362  DOI: Not available
Keywords: Medicine
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