Abstract | BACKGROUND AND OBJECTIVES:
Breast cancer is one of the most common causes of cancer-related deaths in women worldwide. Studies on glucosylceramide synthase (GCS) activity suggest that this enzyme has a role in the development of multidrug resistance in many cancer cells. However, few studies have shown the expression of GCS in invasive ductal breast cancer and breast intraductal proliferative lesions. METHODS: In total, 196 samples from patients with invasive ductal breast cancer and 61 samples of breast intraductal proliferative lesions were collected. Immunohistochemical analyses were conducted to determine the expression of GCS and other related proteins. RESULTS: Expression of GCS was high in estrogen receptor (ER)-positive and HER-2 negative samples. In contrast, the expression of GCS in invasive ductal cancer was significantly lower than that in intraductal proliferative lesions. CONCLUSION: Our data demonstrates a correlation between the expression of the GCS protein and ER-positive/HER-2 negative breast cancer. Furthermore, in contrast to previous reports, the expression of GCS protein was shown to be much higher in ductal carcinoma in-situ than that in invasive ductal cancer. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/1559854430111589.
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Authors | Jiannan Liu, Ping Sun, Yuan Sun, Aina Liu, Dong You, Fenge Jiang, Yuping Sun |
Journal | Diagnostic pathology
(Diagn Pathol)
Vol. 9
Pg. 22
(Jan 23 2014)
ISSN: 1746-1596 [Electronic] England |
PMID | 24456584
(Publication Type: Journal Article)
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Chemical References |
- Biomarkers, Tumor
- Receptors, Estrogen
- Glucosyltransferases
- ceramide glucosyltransferase
- ERBB2 protein, human
- Receptor, ErbB-2
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Topics |
- Adult
- Aged
- Biomarkers, Tumor
(analysis)
- Breast Neoplasms
(enzymology, genetics, mortality)
- Carcinoma, Ductal, Breast
(enzymology, genetics, mortality)
- Carcinoma, Intraductal, Noninfiltrating
(enzymology, genetics, mortality)
- Female
- Glucosyltransferases
(analysis, biosynthesis)
- Humans
- Immunohistochemistry
- In Situ Hybridization, Fluorescence
- Middle Aged
- Prognosis
- Receptor, ErbB-2
(analysis, biosynthesis, genetics)
- Receptors, Estrogen
(analysis, genetics, metabolism)
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