Suzuki Y, Honma T, Hayashi S, Ajioka Y, Asakura H
Third Department of Internal Medicine, Niigata University School of Medicine, 1-757 Asahimachi-dori, Niigata 951-8510, Japan.
J Clin Pathol. 2002 Mar;55(3):212-6. doi: 10.1136/jcp.55.3.212.
To investigate whether the expression of apoptosis and cell proliferation related proteins is related to the macroscopic form of colorectal neoplasia.
The extent of apoptosis, using the 3' end DNA labelling method, and the immunohistochemical expression of cell proliferation (Ki-67) and apoptosis related proteins (Bcl-2, Bak, and p53) were investigated in 64 colorectal adenomas and 22 early carcinomas extending no further than the upper submucosal region. The specimens were classified into three types of macroscopic form (polypoid, flat, and depressed).
The Ki-67 labelling index and the Bak score did not differ significantly among each macroscopic form. In contrast, the apoptotic index and the Bcl-2 score changed significantly according to the macroscopic forms. Compared with polypoid and flat tumours, depressed tumours had a significantly lower apoptotic index (2.84, 2.28, and 1.44, respectively) and a significantly lower Bcl-2 score (3.18, 2.70, and 1.64, respectively). The proliferation/apoptosis ratio was significantly lower in polypoid tumours than in the other two macroscopic forms. The Bcl-2 score became significantly lower as the tumours flattened or took on a depressed form. Immunohistochemical p53 overexpression did not correlate with the macroscopic forms.
These results suggest that differences in both Bcl-2 expression and apoptosis may play an important role in the morphogenesis of colorectal neoplasia.
研究凋亡及细胞增殖相关蛋白的表达是否与结直肠肿瘤的大体形态有关。
采用3'端DNA标记法研究64例结直肠腺瘤和22例浸润深度不超过黏膜下层上部的早期癌组织中的凋亡程度,并通过免疫组织化学法检测细胞增殖(Ki-67)及凋亡相关蛋白(Bcl-2、Bak和p53)的表达。将标本分为三种大体形态类型(息肉样、扁平样和凹陷样)。
Ki-67标记指数和Bak评分在各大体形态类型之间无显著差异。相反,凋亡指数和Bcl-2评分根据大体形态有显著变化。与息肉样和平坦样肿瘤相比,凹陷样肿瘤的凋亡指数显著更低(分别为2.84、2.28和1.44),Bcl-2评分也显著更低(分别为3.18、2.70和1.64)。息肉样肿瘤的增殖/凋亡比值显著低于其他两种大体形态类型。随着肿瘤变扁平或呈凹陷样,Bcl-2评分显著降低。免疫组织化学检测显示p53过表达与大体形态无关。
这些结果表明,Bcl-2表达和凋亡的差异可能在结直肠肿瘤的形态发生中起重要作用。