Literature DB >> 19075689

The database dbEST correctly predicts gene expression in colon cancer patients.

M Radeva1, T Hofmann, B Altenberg, H Mothes, K K Richter, B Pool-Zobel, K O Greulich.   

Abstract

This study aims to test the predictive power of gene expression data derived from NIH's database dbEST, which collects gene expression results from a large number and variety of DNA array experiments. The motivation of this study is to make comparable experimental studies, which are usually performed only for one or a few tissues or organs, with a wide variety of other tissues. Confirmation of a good predictive power of dbEST would put a number of interesting and partially surprising recent findings, solely based on data mining, on a more solid basis than available so far. The expression of nine genes (eIF4E, DDX6, HAT1, USP28, HSP90(beta, PKM2, PLK1, COX2 and OPN) plus two calibration genes in paired normal and cancer colon tissues of eight individual patients was investigated by quantitative RT-PCR and compared with the predictions made by the data-base. GUS and beta-actin reveal only little variation among different patients, making them good internal calibration standards. In normal colon tissue, data mining correctly predicts the expression of all nine genes, which covers two orders of magnitude. In cancer, dbEST is somewhat less precise, but still valuable for the comparison with clinical results.

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Year:  2008        PMID: 19075689     DOI: 10.2174/138920108786786330

Source DB:  PubMed          Journal:  Curr Pharm Biotechnol        ISSN: 1389-2010            Impact factor:   2.837


  4 in total

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2.  USP28 is a potential prognostic marker for bladder cancer.

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3.  Defensin alpha 6 (DEFA 6) overexpression threshold of over 60 fold can distinguish between adenoma and fully blown colon carcinoma in individual patients.

Authors:  Mariya Y Radeva; Franziska Jahns; Anne Wilhelm; Michael Glei; Utz Settmacher; Karl Otto Greulich; Henning Mothes
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4.  USP28 facilitates pancreatic cancer progression through activation of Wnt/β-catenin pathway via stabilising FOXM1.

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  4 in total

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