Drachenberg C B, Ioffe O B, Papadimitriou J C
Department of Pathology, University of Maryland School of Medicine, Baltimore 21201, USA.
Arch Pathol Lab Med. 1997 Jan;121(1):54-8.
Apoptosis has attracted significant attention in the study of tumors during recent years. The first goal of this study was to evaluate the number of apoptotic cells and bodies in benign glands, in high-grade prostatic intraepithelial neoplasia, and in malignant prostatic glands. The second objective was to compare the effectiveness of in situ end-labeling of fragmented DNA (ISEL) with the use of routine hematoxylin-eosin (H&E) stains in the assessment of apoptosis rates.
The percentage of apoptosis was measured with ISEL and H&E stains in sections from 16 prostatectomies performed for previously untreated peripheral prostatic adenocarcinomas.
Both methods showed progressive increase of the rates of apoptosis from benign glands (0.34% 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 rate in prostatic intraepithelial neoplasia and carcinomas is one more indication of the continuum in the pathogenetic process leading to invasive prostatic carcinoma. Student's t test revealed no statistically significant difference in the percentage of apoptosis rendered by ISEL and H&E staining.
From a practical point of view, evaluation of apoptosis with H&E stains can be readily performed using routine clinical material. The procedure is inexpensive, and it gives good tissue morphology. However, quantitative measurements may be time-consuming and observer-dependent. The apoptotic bodies are clearly identifiable with ISEL, making quantitation easy and even amenable to automated counting methods. Disadvantages of ISEL are significantly higher costs and poor tissue morphology. We conclude that accurate evaluation of apoptosis may be performed reliably with both routine H&E staining and the ISEL method. The decision to choose one method over the other depends on the economic resources available and the amount of material to be evaluated.
近年来,细胞凋亡在肿瘤研究中备受关注。本研究的首要目标是评估良性腺体、高级别前列腺上皮内瘤变以及恶性前列腺腺体中凋亡细胞和凋亡小体的数量。第二个目标是比较在评估凋亡率时,DNA片段原位末端标记法(ISEL)与常规苏木精-伊红(H&E)染色法的有效性。
对16例因未经治疗的外周前列腺腺癌而进行前列腺切除术的标本切片,采用ISEL和H&E染色法测量凋亡百分比。
两种方法均显示凋亡率从良性腺体(0.34%至0.38%)、高级别前列腺上皮内瘤变(1.44%至1.39%)到癌(2.69%至2.75%)呈逐渐增加趋势。前列腺上皮内瘤变和癌中凋亡率的增加进一步表明了导致侵袭性前列腺癌的发病过程具有连续性。学生t检验显示,ISEL和H&E染色法所呈现的凋亡百分比无统计学显著差异。
从实际角度来看,使用常规临床材料通过H&E染色法即可轻松评估细胞凋亡。该方法成本低廉,且能提供良好的组织形态。然而,定量测量可能耗时且依赖观察者。ISEL能清晰识别凋亡小体,便于定量,甚至适用于自动计数方法。ISEL的缺点是成本显著更高且组织形态不佳。我们得出结论,常规H&E染色法和ISEL法均可可靠地进行细胞凋亡的准确评估。选择一种方法而非另一种方法的决定取决于可用的经济资源和待评估材料的数量。