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Research ArticleExperimental Studies

Expression of E-Cadherin, β-Catenin and APC protein in Canine Colorectal Tumours

BRUNELLA RESTUCCI, MANUELA MARTANO, GIONATA DE VICO, LORENZO LO MUZIO and PAOLA MAIOLINO
Anticancer Research August 2009, 29 (8) 2919-2925;
BRUNELLA RESTUCCI
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  • For correspondence: restucci@unina.it
MANUELA MARTANO
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GIONATA DE VICO
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LORENZO LO MUZIO
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PAOLA MAIOLINO
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    Figure 1.

    A, Well-differentiated papillary adenocarcinoma showing APC protein to be strongly expressed by many cells. The immunolabelling is evident at the luminal pole of neoplastic cells. (Streptavidin-biotin peroxidase; Bar=20 μm); B, Well-differentiated papillary adenocarcinoma. Cytoplasmic β-catenin distribution with nuclear positivity is evident in some cells (arrows). Membranous distribution is also shown. (Streptavidin-biotin peroxidase; Bar=20 μm); C, Poorly differentiated tubular adenocarcinoma. Immunostaining for APC protein showing complete negativity (Streptavidin-biotin peroxidase; Bar=20 μm); D, Poorly differentiated tubular adenocarcinoma showing β-catenin distributed in the cytoplasm of many neoplastic cells. (Streptavidin-biotin peroxidase; Bar=20 μm); E, Dysplasia. β-Catenin immunostaining, corresponding to red TRITC immunofluorescence, with a membranous distribution in many cells. Cytoplasmic distribution is evident in few cells. (Two-colour immunofluorescence. Bar=40 μm); F, Dysplasia. APC immunostaining, corresponding to green FITC imunofluorescence, with strong expression in many cells. (Two-colour immunofluorescence. Bar=40 μm); G, Dysplasia. Coexpression of APC and β-catenin, evident in yellow, shows the colocalization of both protein in many cells. (Two-colour immunofluorescence. Bar=40 μm); H, Well-differentiated tubular adenocarcinoma. β-Catenin immunostaining, corresponding to red TRITC immunofluorescence, is membranous in many cells. Cytoplasmic distribution is evident in some neoplastic cells (arrows). (Two-colour immunofluorescence. Bar=40 μm); I, Well-differentiated tubular adenocarcinoma. APC protein immunostaining, corresponding to green FITC imunofluorescence, with weak expression in many cells and negativity in the cells with cytoplasmic β-catenin distribution (arrows). (Two-colour immunofluorescence. Bar=40 μm); J, Well-differentiated tubular adenocarcinoma. Coexpression of both β-catenin and APC protein confirms the cytoplasmic distribution of β-catenin in APC-negative cells (arrows). (Two-colour immunofluorescence. Bar=40 μm); K, Poorly differentiated tubular adenocarcinoma. β-Catenin immunostaining, corresponding to red TRITC immunofluorescence, with cytoplasmic distribution in many neoplastic cells (arrows). (Two-colour immunofluorescence. Bar=40 μm); L, Poorly differentiated tubular adenocarcinoma. APC protein immunostaining, corresponding to green FITC imunofluorescence, shows the absence of protein in many neoplastic cells (arrows). (Two-colour immunofluorescence. Bar=40 μm); M, Poorly differentiated tubular adenocarcinoma. Coexpression of both β-catenin and APC protein confirms the cytoplasmic distribution of β-catenin in APC-negative cells (arrows). (Two-colour immunofluorescence. Bar=40 μm);

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    Figure 2.

    Comparison of the percentage of cells immunolabelled with E-cadherin, β-catenin and APC in normal, dysplastic and neoplastic samples of canine colon.

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Anticancer Research: 29 (8)
Anticancer Research
Vol. 29, Issue 8
August 2009
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Expression of E-Cadherin, β-Catenin and APC protein in Canine Colorectal Tumours
BRUNELLA RESTUCCI, MANUELA MARTANO, GIONATA DE VICO, LORENZO LO MUZIO, PAOLA MAIOLINO
Anticancer Research Aug 2009, 29 (8) 2919-2925;

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Expression of E-Cadherin, β-Catenin and APC protein in Canine Colorectal Tumours
BRUNELLA RESTUCCI, MANUELA MARTANO, GIONATA DE VICO, LORENZO LO MUZIO, PAOLA MAIOLINO
Anticancer Research Aug 2009, 29 (8) 2919-2925;
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