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Solin, L.J., Gray, R., Baehner, F.L., Butler, S.M., Hughes, L.L., Yoshizawa, C., Cherbavaz, D.B., Shak, S., Page, D.L., Sledge, G.W., Davidson, N.E., Ingle, J.N., Perez, E.A., Wood, W.C., Sparano, J.A. and Badve, S. (2013) A Multigene Expression Assay to Predict Local Recurrence Risk for Ductal Carcinoma In Situ of the Breast. Journal of the National Cancer Institute, 105, 701-710.
https://doi.org/10.1093/jnci/djt067
has been cited by the following article:
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TITLE:
Immunohistochemical Biomarkers in Ductal Carcinoma In Situ
AUTHORS:
I. Petrone, F. Resende Rodrigues, P. Valverde Fernandes, E. Abdelhay
KEYWORDS:
Breast Cancer, Ductal Carcinoma In Situ, Immunohistochemistry, Biomarker Proteins, Categorization
JOURNAL NAME:
Open Journal of Pathology,
Vol.10 No.4,
September
21,
2020
ABSTRACT:
Introduction: Breast ductal carcinoma In Situ (DCIS) can be defined as a malignant epithelial proliferation with growth limited by the basal membrane of the ductal epithelium, with no evidence of stromal invasion. There has been a trend of trying to subcategorize DCIS based on cell proliferation assays (Ki67) and the expression of hormone receptors and the human epidermal growth receptor (HER-2) as detected by immunohistochemistry, similar to invasive breast carcinomas (IBC). The aims were to evaluate the expression of breast cancer marker proteins in DCIS by immunohistochemistry to better categorize it. Methods: 46 biopsies from women with DCIS and IBC Luminal A-like were evaluated by immunohistochemistry staining of proteins already known to be biomarkers in IBC. For controls, normal breast tissue from mammoplasty (n = 3) was used. Results: Our results showed an increase of estrogen receptor (ER) and progesterone receptor (PR) expression relative to that in normal tissue samples (p Conclusion: The biology of DCIS is not well understood given the complexity and heterogeneity of the disease, which makes it important to better sub-categorize this tumor, especially considering the possibility of identifying DCIS cases with the potential for recurrence and evolution into IBC.
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