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Gene expression fingerprint of uterine serous papillary carcinoma: identification of novel molecular markers for uterine serous cancer diagnosis and therapy
A D Santin, F Zhan, S Cane', S Bellone, M Palmieri, M Thomas, A Burnett, J J Roman, M J Cannon, J Shaughnessy Jr and S Pecorelli
BACK TO ARTICLEFigure 1.
Unsupervised hierarchical clustering of 15 primary uterine cell lines (i.e., 10 USPC and five NEC). The cluster is colour coded using red for upregulation, green for downregulation, and black for median expression. Agglomerative clustering of genes is illustrated with dendrograms.
Full figure and legend (129K)Figure 2.
Quantitative RT–PCR and microarray expression analysis of CDKN2A/p16, CDKN2A/p14ARF, claudin-3, claudin-4, GRB-7 and c-erbB2 genes differentially expressed between USPC and NEC. Quantitative RT-PCR data were highly correlated to the microarray data (P<0.001).
Full figure and legend (66K)Figure 3.
Representative immunohistochemical staining for claudin-4 on two paraffin-embedded USPC specimens (B–C) and one NEC specimen (A). Normal endometrial cell 1 (upper panel) showed light membrane staining for claudin-4, while USPC 1 and USPC 3 showed heavy cytoplasmic and membranous staining for claudin-4 (middle and lower panel). Note the large difference in the size of USPC cells when compared to the control glandular epithelium of a menopausal women. Original magnification
400.
Figure 4.
Representative dose-dependent CPE-mediated cytotoxicity of primary USPC compared to positive control Vero cells or negative controls (i.e., NEC, fibroblasts, and monocytes) after 24 h exposure to scalar doses of CPE. VERO, positive control cells. Uterine serous papillary carcinoma-1 to USPC-3 primary uterine serous tumors. NEC, normal endometrial cells. Fibroblasts, normal human fibroblasts. Monocytes, normal mononuclear cells.
Full figure and legend (58K)