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Tumor Biology

Cyclooxygenase-2 Expression in Human Esophageal Carcinoma

Katja C. Zimmermann, Mario Sarbia, Artur-Aron Weber, Franz Borchard, Helmut E. Gabbert and Karsten Schrör
Katja C. Zimmermann
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Mario Sarbia
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Artur-Aron Weber
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Franz Borchard
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Helmut E. Gabbert
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Karsten Schrör
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DOI:  Published January 1999
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    Fig. 1.

    Examples of cytoplasmatic COX-2 immunoreactivity (brown reaction product) in all cell layers of normal esophageal squamous epithelium (a), in smooth muscle cells of the esophageal wall (arrow) together with unreactive cells of a SCC (*; b). Focal COX-2 immunoreactivity in a moderately differentiated SCC of the esophagus (arrow; c). No COX-2 immunoreactivity in metaplastic Barrett’s mucosa (positive reaction in fibroblastic stromal cells; *; d), in contrast to a moderately differentiated ADC of the esophagus (e). COX-2 immunostaining in cells of the permanent esophageal carcinoma cell line OSC-2 (f).

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    Fig. 2.

    Western blot demonstrating COX-2 and COX-1 protein expression in seven esophageal SCC samples (Ca-1–7) compared with normal esophageal squamous epithelium (Normal-1). The corresponding COX-2 protein expression levels, quantified by immunohistochemistry (Imm.hist.) according to an immunoreactive scoring system (see “Materials and Methods”), are indicated below the image.

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    Fig. 3.

    A, RT-PCR products of COX-1 and COX-2 mRNA in esophageal SCC cell lines OSC-1 and OSC-2. B, Western blot demonstrating COX-2 and COX-1 protein expression in esophageal SCC cell lines OSC-1 and OSC-2.

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    Fig. 4.

    Bicyclo-PGE2 release (A) and 6-keto-PGF1α (B) release by esophageal SCC cells. Data are mean ± SE from four independent experiments.

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    Fig. 5.

    Inhibition of bicyclo-PGE2 formation in esophageal SCC cells with selective COX-2 inhibitors flosulide and NS-398. Data are mean ± SE from three independent experiments. *, P < 0.05 versus control.

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    Fig. 6.

    Inhibition of cell proliferation with selective COX-2 inhibitors flosulide and NS-398. Data are mean ± SE from five independent experiments. *, P < 0.05 versus control.

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    Fig. 7.

    Induction of apoptosis in OSC-2 tumor cells by the selective COX-2 inhibitor flosulide as determined by light microscopy. Data are percentages of mean number of apoptotic bodies/100 intact tumor cells.

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    Fig. 8.

    Numerous apoptotic OSC-2 cells after treatment with 100 μm flosulide (H&E).

Tables

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  • Table 1

    Expression of COX-2 in 172 SCCs and in 27 ADCs of the esophagus as determined by immunohistochemistry

    A. Percentage of positive tumor cellsa
    01234
    SCC1639363843
    ADC63567
    B.Staining intensityb
    01+2+
    SCC1610947
    ADC6714
    C.Immunoreactive scorec
    012345678
    SCC163034382911734
    ADC622725201
    • a Percentage of positive cells: 0, 0–4%; 1, 5–24%; 2, 25–49%; 3, 50–74%; 4, 75–100%.

    • b Staining intensity: 0, negative; 1+, weak; 2+, strong.

    • c Immunoreactive score: combination of a and b (see “Materials and Methods”).

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January 1999
Volume 59, Issue 1
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Cyclooxygenase-2 Expression in Human Esophageal Carcinoma
Katja C. Zimmermann, Mario Sarbia, Artur-Aron Weber, Franz Borchard, Helmut E. Gabbert and Karsten Schrör
Cancer Res January 1 1999 (59) (1) 198-204;

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Cyclooxygenase-2 Expression in Human Esophageal Carcinoma
Katja C. Zimmermann, Mario Sarbia, Artur-Aron Weber, Franz Borchard, Helmut E. Gabbert and Karsten Schrör
Cancer Res January 1 1999 (59) (1) 198-204;
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