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Research ArticleClinical Studies

Impact of Mistletoe Lectin Binding in Breast Cancer

PETER FRITZ, JÜRGEN DIPPON, THOMAS KIERSCHKE, ISABEL SIEGLE, ALEXANDRA MÖHRING, ADINA MOISA and THOMAS E. MÜRDTER
Anticancer Research March 2004, 24 (2C) 1187-1192;
PETER FRITZ
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JÜRGEN DIPPON
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THOMAS KIERSCHKE
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ISABEL SIEGLE
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ALEXANDRA MÖHRING
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ADINA MOISA
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THOMAS E. MÜRDTER
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Abstract

Background: One of the most often used complementary or alternative anticancer therapeutics for breast cancer is mistletoe extract with Viscum album lectin (VAA-1) as the leading component. The aim of this study was to determine the correlation between VAA-1 binding in breast cancer and disease outcome. Materials and Methods: VAA-1 binding to either tumour cells or tumour infiltrating inflammatory cells was examined by immunohistochemical staining of paraffin tissue sections from breast cancer patients (n=226). Results: About 34% of breast cancer tumour cells displayed a strong VAA-1 binding. Kaplan-Meier statistics revealed an inverse correlation between disease outcome and presence of strong VAA-1 binding to tumour cells. Conclusion: As binding of VAA-1 indicates the presence of galactose molecules in saccharide structures of the cytoplasm or cell membrane, we conclude that the amount of galactose-containing glycoproteins, mucoproteins and glycolipids in breast cancer tumour cells is related to disease outcome.

Footnotes

    • Received October 2, 2003.
    • Accepted February 18, 2004.
  • Copyright© 2004 International Institute of Anticancer Research (Dr. John G. Delinassios), All rights reserved
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Anticancer Research
Vol. 24, Issue 2C
March-April 2004
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Impact of Mistletoe Lectin Binding in Breast Cancer
PETER FRITZ, JÜRGEN DIPPON, THOMAS KIERSCHKE, ISABEL SIEGLE, ALEXANDRA MÖHRING, ADINA MOISA, THOMAS E. MÜRDTER
Anticancer Research Mar 2004, 24 (2C) 1187-1192;

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Impact of Mistletoe Lectin Binding in Breast Cancer
PETER FRITZ, JÜRGEN DIPPON, THOMAS KIERSCHKE, ISABEL SIEGLE, ALEXANDRA MÖHRING, ADINA MOISA, THOMAS E. MÜRDTER
Anticancer Research Mar 2004, 24 (2C) 1187-1192;
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