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Using histology, all rabbit mammary adenocarcinomas show areas with non-neoplastic myoepithelial cells (ME cells) and areas of invasive carcinoma: (A) Depicted is an area composed of neoplastic cells arranged in tubular and cystic structures (asterisks) with multifocal infiltration of the stroma (thin arrows). Hematoxylin-eosin (HE)-stained (B) tubular structures are lined by tumor cells (thin arrow) and are surrounded by ME cells. These are spindle-shaped (white arrowhead) or cuboidal to polygonal (black arrowhead). The thick arrow labels a tumor cell with a mitotic figure.

Using histology, all rabbit mammary adenocarcinomas show areas with non-neoplastic myoepithelial cells (ME cells) and areas of invasive carcinoma: (A) Depicted is an area composed of neoplastic cells arranged in tubular and cystic structures (asterisks) with multifocal infiltration of the stroma (thin arrows). Hematoxylin-eosin (HE)-stained (B) tubular structures are lined by tumor cells (thin arrow) and are surrounded by ME cells. These are spindle-shaped (white arrowhead) or cuboidal to polygonal (black arrowhead). The thick arrow labels a tumor cell with a mitotic figure.

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Most mammary tumors in pet rabbits are carcinomas; prognostic factors are unknown. The aim of this study on rabbit mammary carcinomas was to determine the expression of myoepithelial markers that have a prognostic relevance in human cancers. Mammary carcinomas (n = 119) of female or female-spayed pet rabbits were immunostained for cytokeratin AE1/A...

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Context 1
... hematoxylin-eosin-stained tissue section-in addition to epithelial areas entirely composed of tumor cells-all rabbit mammary carcinomas contained nests of tumor cells delineated by spindle-shaped, cuboidal, or polygonal cells, suggestive of retained non-neoplastic ME cells (Figure 2). Epithelial tumor areas and the involved epithelial cell populations were further characterized by immunohistochemistry and image analysis. ...
Context 2
... CK-positive area was significantly larger than the epithelial tumor areas positive for SMA (p = 5.11 × 10 −3 ), vimentin (p = 1.06 × 10 −5 ), and calponin (p = 9.17 × 10 −9 ). The stained areas for SMA, vimentin, and calponin showed a mild, gradual increase in size ( Figure S2). The medians for the positive areas of vimentin (47.95%) and SMA (45.08%) were similar, whereas the median of calponin (52.53%) was higher, and CK showed the highest median value (78.09%) (Table 3; Figure S2). ...
Context 3
... stained areas for SMA, vimentin, and calponin showed a mild, gradual increase in size ( Figure S2). The medians for the positive areas of vimentin (47.95%) and SMA (45.08%) were similar, whereas the median of calponin (52.53%) was higher, and CK showed the highest median value (78.09%) (Table 3; Figure S2). Similar results were obtained by consideration not only of the size of the immunopositive area, but also of the obtained staining intensities. ...
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... CK-positive area was significantly larger than the epithelial tumor areas positive for SMA (p = 5.11 × 10 −3 ), vimentin (p = 1.06 × 10 −5 ), and calponin (p = 9.17 × 10 −9 ). The stained areas for SMA, vimentin, and calponin showed a mild, gradual increase in size ( Figure S2). The medians for the positive areas of vimentin (47.95%) and SMA (45.08%) were similar, whereas the median of calponin (52.53%) was higher, and CK showed the highest median value (78.09%) (Table 3 and Figure S2). ...
Context 5
... stained areas for SMA, vimentin, and calponin showed a mild, gradual increase in size ( Figure S2). The medians for the positive areas of vimentin (47.95%) and SMA (45.08%) were similar, whereas the median of calponin (52.53%) was higher, and CK showed the highest median value (78.09%) (Table 3 and Figure S2). Similar results were obtained by consideration not only of the size of the immunopositive area, but also of the obtained staining intensities. ...
Context 6
... Materials: The following are available online at http://www.mdpi.com/2076-2615/9/10/740/s1, Figure S1: Negative and positive controls for the immunostaining of rabbit mammary carcinomas for cytokeratin AE1/AE3, smooth muscle actin, vimentin and calponin, Figure S2: Image analysis to determine immunopositive areas for smooth muscle actin, vimentin, calponin and cytokeratin AE1/AE3, Figure S3: Median values for smooth-muscle actin-, vimentin-and calponin-immunostaining of spindle-shaped and hyperplastic non-neoplastic myoepithelial cells, Figure S4: Association between percentages of spindle-shaped and hypertrophic myoepithelial cells and the age of the rabbits, Figure S5: Scatter plots to depict the relationship between calponin-positive tumor cells and the size of the tumor area with a tubular growth or the mitotic count, respectively. ...

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