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Metallothionein as an epithelial proliferative compartment marker for DNA flow cytometry
H H Meskel1, M G Cherian, V J Martinez
1Department of Pathology, University of Western Ontario, London, Canada.
Summary
Metallothionein (MT) antibody effectively identifies epithelial cells in archival tissue samples. This marker aids in DNA flow cytometry, highlighting proliferating cells and improving cancer diagnostics.
Area of Science:
- Oncology
- Cell Biology
- Biochemistry
Background:
- Metallothionein (MT) is a low molecular weight protein involved in metal binding.
- MT antibody preferentially stains the proliferative edge of epithelial tumors in paraffin sections.
- Epithelial cell markers are crucial for accurate analysis in flow cytometry.
Purpose of the Study:
- To demonstrate the utility of the MT antibody as an epithelial cell marker in DNA flow cytometry.
- To evaluate MT staining for ploidy and cell cycle assessment in archival specimens.
- To investigate the potential of MT as an index of malignancy by identifying proliferating epithelial cells.
Main Methods:
- DNA flow cytometry was performed on archival specimens, including control breast and colon tissues, and breast and colon adenocarcinomas.
- Specimens were stained for both DNA and MT.
- Immunohistochemical staining was used to confirm MT's specificity for epithelial cells.
Main Results:
- MT antibody stained epithelial cells effectively in both control and cancerous tissues.
- The S-phase fraction (SPF), a measure of cell turnover, was significantly higher in MT-stained preparations compared to unstained ones, particularly in adenocarcinomas.
- MT staining identified a higher percentage of proliferating malignant epithelial cells, with an average of 47% of aneuploid cells showing MT staining.
Conclusions:
- MT antibody is a valuable tool for identifying epithelial cells in DNA flow cytometry of archival specimens.
- MT staining enhances the evaluation of cell ploidy and cell cycle, especially in cancer diagnostics.
- The preferential staining of proliferating cells by MT suggests its potential as a marker for malignancy.