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PMID: 11438448 Published · ppublish English Journal Article

Circulating breast cancer cells are frequently apoptotic.

The American journal of pathology ·Vol. 159 ·No. 1 ·2001-07-00 ·Pages 17-20

Méhes G, Witt A, Kubista E, Ambros PF

Abstract

Automatic search for cytokeratin/mucin-1 double immunofluorescence was performed to detect and characterize circulating epithelial tumor cells in patients with advanced breast cancer. The peripheral blood samples in 8 of 19 patients (42.1%) presented with cytokeratin-positive and epithelial-type mucin-positive (CK(+)/MUC1(+)) tumor cells. Detailed microscopic analysis, however, suggested that the majority of the double immunopositive cells was apoptotic according to an "inclusion type" cytokeratin staining pattern and nuclear condensation. Furthermore, apoptosis-related DNA strand breaks could be demonstrated by applying the TdT-uridine nick end labeling assay in these cells. In 3 of 8 positive samples all of the CK(+)/MUC1(+) cells displayed apoptotic features. We conclude that apoptotic cells significantly contribute to the circulating tumor cell fraction in breast cancer patients. As the predictive value of such cells for the outcome of the disease is unclear, they should be considered separately when analyzing tumor cell dissemination.

MeSH Terms
Apoptosis Breast Neoplasms/blood,genetics,metabolism,pathology DNA Damage Female Fluorescent Antibody Technique Humans Image Processing, Computer-Assisted In Situ Nick-End Labeling Keratins/metabolism Microscopy, Fluorescence Mucin-1/metabolism Neoplastic Cells, Circulating/metabolism,pathology
Chemicals
Mucin-1 Keratins
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Méhes G
Children's Cancer Research Institute, St. Anna Kinderspital, Vienna. Vienna General Hospital, Vienna, Austria.
Witt A
Kubista E
Ambros P F
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Article Info
Journal
The American journal of pathology
Abbr.
Am J Pathol
ISSN
0002-9440
Published
2001-07-00
Pages
17-20
Language
English
Region
United States
NLM ID
0370502
PMCID
PMC1850424
Subset
IM
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