Myxovirus (influenza virus) resistance A (MxA) is an interferon regulated protein responsible for a specific antiviral state against viral infection. Our lab has previously shown that MxA is up-regulated by androgens in the normal prostate epithelial cells; however, there is no known role for MxA in cancer. Meta-analysis of different expression databases (e.g. NCBI GEO and Oncomine) suggested a strong inverse association between MxA expression and prostate cancer. To confirm these studies, we performed immunohistochemistry on normal prostate and prostate cancer tissues. Our results revealed that MxA expression was indeed decreased in cancerous as compared to normal prostate, indicating that MxA could be transcriptionally down-regulated in cancer. Previous studies indicated that MxA down-regulation could be due to a specific polymorphism in the proximal MxA promoter at position -88. This single nucleotide polymorphism G>T (rs2071430) is involved in modifying the gene expression and interestingly, it harbors an interferon-stimulated response element (ISRE) that is required for expression in response to interferons. The "T" allele restores whereas the "G" allele attenuates ISRE binding, resulting in increased or decreased MxA expression, respectively. Based on these observations we hypothesized that decreased expression of MxA in prostate cancer could be due to the rs2071430 polymorphism. We investigated this polymorphism in genomic DNA from equal number of disease free and prostate cancer samples. The results provide evidence that the GG genotype (low promoter activity) is higher in PCa (72%) as compared to normal (58.6%). The TT genotype (high activity) was higher in normal (5.7%) compared to PCa (2.4%) p
Identifer | oai:union.ndltd.org:auctr.edu/oai:digitalcommons.auctr.edu:dissertations-2275 |
Date | 01 July 2013 |
Creators | Glymph, Shanora Elizabeth |
Publisher | DigitalCommons@Robert W. Woodruff Library, Atlanta University Center |
Source Sets | Atlanta University Center |
Detected Language | English |
Type | text |
Format | application/pdf |
Source | ETD Collection for Robert W. Woodruff Library, Atlanta University Center |
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