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. 2007 Apr;98(4):484-90.
doi: 10.1111/j.1349-7006.2007.00430.x. Epub 2007 Feb 16.

Immunohistochemical expression of the beta-catenin-interacting protein B9L is associated with histological high nuclear grade and immunohistochemical ErbB2/HER-2 expression in breast cancers

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Immunohistochemical expression of the beta-catenin-interacting protein B9L is associated with histological high nuclear grade and immunohistochemical ErbB2/HER-2 expression in breast cancers

Hiroyuki Toya et al. Cancer Sci. 2007 Apr.

Abstract

B9L/BCL9-2, a novel beta-catenin-interacting protein, plays an important role in colorectal carcinogenesis by translocating beta-catenin to the nucleus and enhancing beta-catenin-T-cell factor-mediated transcription. To elucidate the role of B9L in breast cancers, we studied B9L expression in ductal carcinoma in situ (DCIS) and invasive ductal carcinoma (IDC) of the breast immunohistochemically and compared it to the immunohistochemical expression of known proteins involved in breast carcinogenesis. In breast tissues, B9L immunoreactivity was present exclusively in the nuclei of normal and neoplastic ductal cells. In DCIS, immunohistochemical B9L expression was significantly associated with the tumor nuclear grade, comedo necrosis and the expression of ErbB2/HER-2, c-myc and p53. In IDC, B9L expression was correlated with ErbB2/HER-2 expression and tumor nuclear grade only. In both DCIS and IDC, immunohistochemical B9L expression was not related to the expression of cytoplasmic beta-catenin. We demonstrated that nuclear B9L expression was closely associated with the high nuclear grade cancer phenotype and the expression of ErbB2/HER-2 in breast cancers.

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Figures

Figure 1
Figure 1
Immunohistochemical results for B9L in ductal carcinoma in situ (DCIS). (a) B9L immunoreactivity of normal breast tissues (×200). (b) Low nuclear grade DCIS (score 0, ×200). (c) Intermediate nuclear grade DCIS (score 1+, ×200). (d) High nuclear grade DCIS (score 2+, ×200).
Figure 2
Figure 2
Immunohistochemical results for β‐catenin and ErbB2/HER‐2 in high nuclear grade ductal carcinoma in situ. (a) Hematoxylin–eosin staining (×100). (b) Membranous staining of β‐catenin (score 2+, ×100). (c) Expression of ErbB2/HER‐2 (score 2+, ×100).
Figure 3
Figure 3
Immunohistochemical results for B9L in invasive ductal carcinoma. (a) Solid‐tubular carcinoma, low nuclear grade (score 0, ×100). (b) Solid‐tubular carcinoma, intermediate nuclear grade (score 1+, ×100). (c) Papillotubular carcinoma, high nuclear grade (score 2+, ×100).
Figure 4
Figure 4
Correlation or inverse correlation between cell biological factors and histopathological features in (a) ductal carcinoma in situ and (b) invasive ductal carcinoma. Solid lines show the correlations between cell biological factors and histopathological features. Dotted lines show inverse correlations.

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