Volume 65, Issue 6 pp. 755-761
Human Cancer

Comparative analyses of bone marrow micrometastases in breast and gastric cancer

Ilona Funke

Corresponding Author

Ilona Funke

Departments of Surgery and Gynecology, Klinikum Grosshadern, University of Munich, Munich, Germany

Department of Surgery, Klinikum Grosshadern, Marchioninistrasse 15, 81377 Munich, Germany. Fax: (49) 89-700-4418Search for more papers by this author
Stefanie Fries

Stefanie Fries

Departments of Surgery and Gynecology, Klinikum Grosshadern, University of Munich, Munich, Germany

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Michaela Rolle

Michaela Rolle

Departments of Surgery and Gynecology, Klinikum Grosshadern, University of Munich, Munich, Germany

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Markus M. Heiss

Markus M. Heiss

Departments of Surgery and Gynecology, Klinikum Grosshadern, University of Munich, Munich, Germany

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Michael Untch

Michael Untch

Departments of Surgery and Gynecology, Klinikum Grosshadern, University of Munich, Munich, Germany

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Heinz Bohmert

Heinz Bohmert

Departments of Surgery and Gynecology, Klinikum Grosshadern, University of Munich, Munich, Germany

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Friedrich W. Schildberg

Friedrich W. Schildberg

Departments of Surgery and Gynecology, Klinikum Grosshadern, University of Munich, Munich, Germany

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Karl W. Jauch

Karl W. Jauch

Departments of Surgery and Gynecology, Klinikum Grosshadern, University of Munich, Munich, Germany

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Abstract

This study is a comparative analysis of the prevalence, absolute number and aggregation status of bone marrow micrometastases (BMM) between breast (n = 234) and gastric (n = 102) cancer patients based on a standardized number of 1 × 106 bone marrow-derived cells per patient. Additionally, expression of the epithelial cell adhesion molecule E-cadherin was analyzed on disseminated tumor cells. A positive BMM status was demonstrated in 88/234 breast and 45/102 gastric cancer patients. The presence of CK18+ cells positively correlated with parameters of advanced tumor progression in breast, but not in gastric cancer. Interestingly, 25.2% of the node-negative patients already had micrometastatic cells in the bone marrow at diagnosis. Regarding the absolute number of CK18+ cells and the frequency of CK18+ cell clusters, no significant difference was found between the 2 tumor types. However, clusters consisting of more than 10 CK18+ cells (type II clusters) were present exclusively in breast cancer patients. Additionally, co-expression of CK18 and E-cadherin was detectable in 15/21 micrometastases-positive breast but in only 1/9 gastric cancer patients. While prevalence of micrometastatic cells in bone marrow is discussed as an early indicator for systemic disease, aggregation status and a certain antigen profile might be indicative for site-specific differences in the manifestation pattern of solid metastases. © 1996 Wiley-Liss, Inc.

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