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Advances in Brief

Expression Profiling Reveals Hepsin Overexpression in Prostate Cancer

Jeffrey A. Magee, Toshiyuki Araki, Sushama Patil, Torsten Ehrig, Lawrence True, Peter A. Humphrey, William J. Catalona, Mark A. Watson and Jeffrey Milbrandt
Jeffrey A. Magee
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Toshiyuki Araki
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Sushama Patil
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Torsten Ehrig
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Lawrence True
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Peter A. Humphrey
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William J. Catalona
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Mark A. Watson
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Jeffrey Milbrandt
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DOI:  Published August 2001
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  • Fig. 1.
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    Fig. 1.

    Vertical scatter plots demonstrating absolute gene expression levels in individual tumors and benign glands from the initial microarray profiles. In all cases, the lower expression threshold is 70.8, representing the scaled noise of the noisiest GeneChip in the experiment. Scaled average difference values less than the threshold were adjusted to 70.8 and, therefore, overlap. A, genes that vary in tumors relative to normal glands. B, expression levels of Cdk10, serotonin receptor 2B, and Pgm-5 plotted with a reduced Y axis to better demonstrate their ranges of expression. C, genes that vary in metastases relative to primary tumors. Symbols correspond to specific pathological descriptions: A and B, •, tumor; ▴, benign. C, •, metastasis; ▴, primary tumor. Horizontal bars average gene expression in each respective sample set.

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    Fig. 2.

    Vertical scatter plots demonstrating relative expression levels for hepsin and Pgm-5 in an independent set of malignant and nonmalignant samples. By quantitative RT-PCR, these two genes both exhibited significant (P < 0.01 and P < 0.05, respectively) expression differences between malignant and nonmalignant samples in the validation sample set. Horizontal bars, average expression of hepsin and Pgm-5 in malignant and nonmalignant sample sets.

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    Fig. 3.

    In situ hybridization for hepsin expression in the prostate. H&E stains of an adjacent frozen section are shown at right. A and B, a low-power view of a prostate specimen with both benign (arrows) and malignant (arrowheads) epithelia. Hepsin is specifically overexpressed in malignant glands. C and D, a high-power view of malignant prostate epithelia overexpressing hepsin. E and F, a high-power view of PIN lesions that also overexpress hepsin. G and H, a high-power view of benign epithelia within the cancer specimen. Note that the benign glands to not express hepsin at appreciable levels.

Tables

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  • Table 1

    Misregulated genes in benign and malignant prostate samples

    AccessionMean avg differenceMean avg differenceMean fold differenceP
    Genea
     cdk 10L3326471 ± 0b950 ± 519c13.4<0.001
     HepsinX07732186 ± 230b7915 ± 4939c42.5<0.001
     Serotonin receptor 2BX7730771 ± 0b322 ± 161c4.5<0.001
    Gened
     Phosphoglucomutase 5L409331136 ± 373b109 ± 83c10.40.011
    Descriptione
     HMG-CoA reductaseM1105880 ± 27f335 ± 73g4.20.021
     Rad50U6313982 ± 24f333 ± 36g4.10.003
    Geneh
     TYRO3 protein tyrosine kinaseU18934952 ± 301f134 ± 57g7.1<0.001
     Diacylglycerol kinaseX625351294 ± 527f127 ± 97g10.2<0.001
     Pyridoxal kinaseU89606628 ± 487f71 ± 0g8.80.014
     Stabilin 1/KIAA0246D874331240 ± 506f98 ± 24g12.6<0.001
     Protein kinase C, β 1X071091125 ± 541f80 ± 16g14.1<0.001
     ButyrophilinU90552390 ± 196f71 ± 0g5.50.002
     Early growth response 3X63741596 ± 374f71 ± 0g8.00.005
     Early growth response 2J04076881 ± 615f101 ± 12g8.70.009
     G protein α 16M63904913 ± 752f71 ± 0g12.90.016
    • a Up-regulated in tumors relative to normal.

    • b Normal.

    • c Tumor.

    • d Down-regulated in tumors relative to normal.

    • e Up-regulated in metastases relative to primaries.

    • f Primaries.

    • g Mets.

    • h Down-regulated in metastases relative to primaries.

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Cancer Research: 61 (15)
August 2001
Volume 61, Issue 15
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Expression Profiling Reveals Hepsin Overexpression in Prostate Cancer
Jeffrey A. Magee, Toshiyuki Araki, Sushama Patil, Torsten Ehrig, Lawrence True, Peter A. Humphrey, William J. Catalona, Mark A. Watson and Jeffrey Milbrandt
Cancer Res August 1 2001 (61) (15) 5692-5696;

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Expression Profiling Reveals Hepsin Overexpression in Prostate Cancer
Jeffrey A. Magee, Toshiyuki Araki, Sushama Patil, Torsten Ehrig, Lawrence True, Peter A. Humphrey, William J. Catalona, Mark A. Watson and Jeffrey Milbrandt
Cancer Res August 1 2001 (61) (15) 5692-5696;
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