The process of developing a greater understanding of the fundamental molecular mechanisms involved in prostate carcinogenesis will provide insights into the questions that still plague the field of prostate cancer research. The goal of this study was to identify altered genes that may have utility either as biomarkers, for improved diagnostic or prognostic application, or as novel targets important in the pathobiology of prostate cancer. We hypothesize that an improved understanding of the genomic and proteomic alterations associated with prostate cancer will facilitate the identification of novel biomarkers and molecular pathways critical to prostate
carcinogenesis. In order to enhance our knowledge of the molecular alterations associated with prostate cancer, our laboratory performed microarray analysis comparing gene expression in healthy normal prostate to that in prostate cancer tissue. Of the greater than 400 genes with significantly altered expression identified in our study, MT2A, Tacc2, Nell2, FosB, PCP4, and Cyr61 were selected for further evaluation to confirm expression changes and evaluate their potential impact in prostate cancer. Analysis of MT2A, Tacc2, and Nell2 expression patterns failed to demonstrate significant changes between prostate cancer and donor prostate tissue and, therefore, these results do not support their further development as prostate cancer biomarkers. We demonstrated that PCP4 was expressed predominently in the stromal compartment of the prostate and was expressed at similar levels in the stroma of normal and prostate cancer tissue. Interestingly, protein expression of PCP4 in a panel of colon cancer tissues was dramatically higher in adenoma and adenocarcinoma tissues compared to donor and benign colon tissue and, consequently, we feel that PCP4 has more potential as a biomarker in colon cancer than in prostate cancer. We also demonstrated that FosB and Cyr61 were upregulated in prostate cancer tissues over donor prostate tissues. Based on expression analysis of FosB and expression and functional analysis of Cyr61, we believe that these two targets have the greatest potental to be functionally significant in the etiology of prostate cancer.
| Identifer | oai:union.ndltd.org:PITT/oai:PITTETD:etd-04172009-105358 |
| Date | 17 April 2009 |
| Creators | D'Antonio, Katherine Elizabeth Bright |
| Contributors | Luyuan Li, PhD, Dan Johnson, PhD, George Michalopoulos, MD, PhD, Robert Getzenberg, PhD, Beth Pflug, PhD |
| Publisher | University of Pittsburgh |
| Source Sets | University of Pittsburgh |
| Language | English |
| Detected Language | English |
| Type | text |
| Format | application/pdf |
| Source | http://etd.library.pitt.edu/ETD/available/etd-04172009-105358/ |
| Rights | unrestricted, I hereby certify that, if appropriate, I have obtained and attached hereto a written permission statement from the owner(s) of each third party copyrighted matter to be included in my thesis, dissertation, or project report, allowing distribution as specified below. I certify that the version I submitted is the same as that approved by my advisory committee. I hereby grant to University of Pittsburgh or its agents the non-exclusive license to archive and make accessible, under the conditions specified below, my thesis, dissertation, or project report in whole or in part in all forms of media, now or hereafter known. I retain all other ownership rights to the copyright of the thesis, dissertation or project report. I also retain the right to use in future works (such as articles or books) all or part of this thesis, dissertation, or project report. |
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