Nj. Hawkins et al., DETECTION OF APOPTOSIS IN COLORECTAL-CARCINOMA BY LIGHT-MICROSCOPY AND IN-SITU END LABELING, Analytical and quantitative cytology and histology, 19(3), 1997, pp. 227-232
OBJECTIVE: An in situ end labelling reaction (ISEL) was recently descr
ibed for the detection of apoptotic cells in histologic sections. We c
ompared the efficiency and reproducibility of this assay with those of
routine light microscopy using hematoxylin and eosin (H&E) in the qua
ntitation of apoptotic cells in colorectal enticer. STUDY DESIGN: Para
ffin-embedded archival tissues from 15 colorectal carcinomas were used
in the study. ISEL was performed using terminal deoxynucleotidyl tran
sferase, biotinylated deoxyuridine triphosphate and streptavidin-alkal
ine phosphatase. RESULTS: Apoptotic indices determined by the two assa
ys showed a strong positive correlation (Pearson coefficient 0.82), wi
th the ISEL assay detecting twice the number of apoptotic cells as tha
t seen with H&E staining. Both assays showed significant interobserver
and intraobserver variation, while the ISEL assay also showed conside
rable interassay variability and was less cost-effective than H&E in t
he detection of apoptotic cells. CONCLUSION: In the light microscopic
quantitation of apoptosis in colorectal tumors, the ISEL assay offered
no greater reproducibility, and was less cost-effective, than routine
H&E staining.