Diagnosis of prostate cancer using differentially expressed genes in stroma

Abstract Over 1 million prostate biopsies are performed in the U.S. every year. A failure to find cancer is not definitive in a significant percentage of patients due to the presence of equivocal structures or continuing clinical suspicion. We have identified gene expression changes in stroma that c...

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Bibliographic Details
Published inClinical cancer research Vol. 16; no. 19_Supplement; p. B20
Main Authors Jia, Zhenyu, Wang, Yipeng, Sawyers, Anne, Yao, Huazhen, Rahmatpanah, Farahnaz, Xia, Xiao-Qin, Xu, Qiang, Pio, Rebecca, Turan, Tolga, Koziol, James A., Goodison, Steve, Carpenter, Philip, Wang-Rodriguez, Jessica, Simoneau, Anne, Meyskens, Frank, Sutton, Manuel, Lernhardt, Waldemar, Beach, Thomas, McClelland, Michael, Mercola, Dan
Format Journal Article
LanguageEnglish
Published 01.10.2010
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Summary:Abstract Over 1 million prostate biopsies are performed in the U.S. every year. A failure to find cancer is not definitive in a significant percentage of patients due to the presence of equivocal structures or continuing clinical suspicion. We have identified gene expression changes in stroma that can detect tumor nearby. We compared gene expression profiles of 13 biopsies containing stroma near tumor and 15 biopsies from volunteers without prostate cancer. More than a thousand significant expression changes were found and thereafter filtered using large numbers of other expression profiles to eliminate possible age-related genes and genes expressed at detectable levels in tumor cells. A stroma-specific classifier was constructed based on 114 candidate genes and tested on 364 independent samples, including 243 tumor-bearing samples and 121 non-tumor samples (normal biopsies, normal autopsies, remote stroma, as well as stroma within a few millimeters of tumor). The classifier predicted the tumor status of patients using tumor-free samples with an average accuracy of 97.2% (sensitivity = 97.9% and specificity = 88.0%) whereas classifiers trained with sets of 100 randomly generated genes had no diagnostic value. These results indicate that the prostate cancer microenvironment exhibits reproducible changes useful for categorizing the presence of tumor in patients when a prostate sample is derived from near the tumor but does not contain any recognizable tumor.
ISSN:1078-0432
1557-3265
DOI:10.1158/DIAG-10-B20