OBJECTIVE: To describe the laser scanning cytometry (LSC) processing and an
alysis developed for the quantitative analysis of estrogen receptor (EX) co
ntent in routine paraffin sections of breast carcinomas.
STUDY DESIGN: Histologic sections of archival, paraffin-embedded tissues fr
om 30 breast carcinomas were labeled for EX with fluoresceinated monoclonal
antibody. EX expression was quantified by LSC ann expressed as percent pos
itive tumor cells and as histogram distributions of receptor expression per
cell. Duplicate sections of the same tumors were stained for EX by a conve
ntional immunoperoxidase reaction and percent positive tumor cells counted
visually.
RESULTS: Percent EX-positive tumor cells by LSC of immunofluorescence-stain
ed sections correlated well with conventional (visual) counts of immunopero
xidase-stained duplicate sections when the latter were categorized as low,,
intermediate or high percent of positive cells. In addition, the marked va
riation in relative number and displayed in histogram distribution.
CONCLUSION: LSC measurements are fast and objective and can be carried out
on sections of paraffin-embedded tissue after routine processing in the pat
hology laboratory. In addition, LSC data provide the relative number of ER
binding sites per unit of DNA; that may reveal clinically significant skewe
d distributions or sub-populations of tumor cells.