PROGRESSIVE INCREASE OF APOPTOSIS IN PROSTATIC INTRAEPITHELIAL NEOPLASIA AND CARCINOMA - COMPARISON BETWEEN IN-SITU END-LABELING OF FRAGMENTED DNA AND DETECTION BY ROUTINE HEMATOXYLIN-EOSIN STAINING
Cb. Drachenberg et al., PROGRESSIVE INCREASE OF APOPTOSIS IN PROSTATIC INTRAEPITHELIAL NEOPLASIA AND CARCINOMA - COMPARISON BETWEEN IN-SITU END-LABELING OF FRAGMENTED DNA AND DETECTION BY ROUTINE HEMATOXYLIN-EOSIN STAINING, Archives of pathology and laboratory medicine, 121(1), 1997, pp. 54-58
Citations number
38
Categorie Soggetti
Pathology,"Medical Laboratory Technology","Medicine, Research & Experimental
Objective.-Apoptosis has attracted significant attention in the study
of tumors during recent years. The first goal of this study was to eva
luate the number of apoptotic cells and bodies in benign glands, in hi
gh-grade prostatic intraepithelial neoplasia, and in malignant prostat
ic glands. The second objective was to compare the effectiveness of in
situ end-labeling of fragmented DNA (ISEL) with the use of routine he
matoxylin-eosin (H&E) stains in the assessment of apoptosis rates. Met
hods.-The percentage of apoptosis was measured with ISEL and H&E stain
s in sections from 16 prostatectomies performed for previously untreat
ed peripheral prostatic adenocarcinomas. Results.-Both methods showed
progressive increase of the rates of apoptosis from benign glands (0.3
4% to 0.38%), to high-grade prostatic intraepithelial neoplasia (1.44%
to 1.39%), to carcinoma (2.69% to 2.75%). The increase in apoptosis r
ate in prostatic intraepithelial neoplasia and carcinomas is one more
indication of the continuum in the pathogenetic process leading to inv
asive prostatic carcinoma. Student's t test revealed no statistically
significant difference in the percentage of apoptosis rendered by ISEL
and H&E staining. Conclusions.-From a practical point of view, evalua
tion of apoptosis with H&E stains can be readily performed using routi
ne clinical material. The procedure is inexpensive, and it gives good
tissue morphology. However, quantitative measurements may be time-cons
uming and observer-dependent. The apoptotic bodies are clearly identif
iable with ISEL, making quantitation easy and even amenable to automat
ed counting methods. Disadvantages of ISEL are significantly higher co
sts and poor tissue morphology. We conclude that accurate evaluation o
f apoptosis may be performed reliably with both routine H&E staining a
nd the ISEL method. The decision to choose one method over the other d
epends on the economic resources available and the amount of material
to be evaluated.