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Identification of specific nuclear structural protein alterations in human breast cancer

✍ Scribed by Manuel Debald; Sebastian Franken; Lukas Carl Heukamp; Andrea Linke; Matthias Wolfgarten; Klaus-Jürgen Walgenbach; Michael Braun; Christian Rudlowski; Volkmar Gieselmann; Walther Kuhn; Gunther Hartmann; Gisela Walgenbach-Brünagel


Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
419 KB
Volume
112
Category
Article
ISSN
0730-2312

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✦ Synopsis


Abstract

Breast cancer is the most commonly diagnosed type of cancer and a major cause of death in women. Reliable biomarkers are urgently needed to improve early detection or to provide evidence of the prognosis for each individual patient through expression levels in tumor tissue or body fluids. This proteomic analysis focused on the nuclear structure of human breast cancer tissue, which has been shown to be a promising tool for cancer biomarker development. The nuclear matrix composition of human breast cancer (n = 14), benign controls (n = 2), and healthy controls (n = 2) was analyzed by high‐resolution two‐dimensional gel electrophoresis and mass spectrometry. Validation studies were performed in an individual sample set consisting of additional breast cancer tissues (n = 3) and additional healthy control tissues (n = 2) by one‐dimensional immunoblot. In this setting, we identified five proteins that were upregulated in human breast cancer tissue, but absent in the healthy and benign controls (P < 0.001). These spots were also present in the investigated human breast cancer cell lines, but absent in the MCF10a cell line, which represents normal human epithelial breast cells. Two of the breast cancer‐specific proteins have been confirmed to be calponin h2 and calmodulin‐like protein 5 by one‐dimensional immunoblot. This is the first study demonstrating the expression of both proteins in human breast cancer tissue. Further studies are required to investigate the potential role of these proteins as biomarkers for early diagnosis or prognosis in human breast cancer. J. Cell. Biochem. 112: 3176–3184, 2011. © 2011 Wiley Periodicals, Inc.


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