Radović Svjetlana, Vukobrat-Bijedić Zora, Selak Ivan, Babić Mirsad
Institute of Pathology, Faculty of Medicine, University of Sarajevo, Cekalusa 90, 71000 Sarajevo, Bosnia and Herzegovina.
Bosn J Basic Med Sci. 2006 Feb;6(1):39-45. doi: 10.17305/bjbms.2006.3208.
The aim of the study was to define the distribution of p53, bcl-2 and Ki-67 proteins in the inflammatory-regenerative and dysplastic lesions of the colon mucosa. The relationship between the presentation of p53, bcl-2 and Ki-67 proteins and the intensity of the inflammatory-regenerative and dysplastic lesions in the colon flat mucosa was investigated as well. Biopsy specimens from 270 patients were examined: 74 were classified as inflammatory-regenerative and 196 as dysplastic lesions (108 mild, 58 moderate, and 30 severe dysplasia). The expression of all three proteins was assessed on the basis of location, quantity, and intensity of immunostaining, by counting antigen positive cells, in comparison with normal mucosa and adenocarcinoma. p53 protein appears only in sporadic cases (6.6%) of severe dysplasia. Bcl-2 expression appears significantly (p<0.005) more often in cases of mild dysplasia (61.1%) compared to inflammatory-regenerative mucosa (14.8%). In cases of mild dysplasia, bcl-2 positive cells were spreading from the lower third to the middle third of the crypts. Bcl-2 expression was maintained through the stadiums of moderate and severe dysplasia (75.8%), where antigen positive cells were found all along the crypts. A significant increase (p<0.005) in the expression of nuclear protein Ki-67 was noticed in the stadiums of moderate (labelling index =26.3) compared to mild dysplasia (labelling index=16.7), and severe (labelling index=36.7) compared to moderate dysplasia, where the zone of cellular proliferation was widen along the whole crypt length. In the process of the development of epithelial dysplasia in the flat mucosa of colon a degree of the gene p53 alteration is low and appears only in sporadic cases of severe dysplasia. Mutation of the bcl-2 gene is involved in the genesis of the lesion but not in its progression to carcinoma. Increased expression of Ki-67 protein speaks in favour of an increased cellular proliferation which, together with the above mentioned mechanisms, is involved in the process of occurrence and progression of epithelial dysplasia in the flat mucosa of colon.
本研究的目的是确定p53、bcl-2和Ki-67蛋白在结肠黏膜炎症再生性病变和发育异常病变中的分布情况。同时也研究了p53、bcl-2和Ki-67蛋白的表达与结肠扁平黏膜炎症再生性病变和发育异常病变程度之间的关系。对270例患者的活检标本进行了检查:74例被分类为炎症再生性病变,196例为发育异常病变(108例轻度、58例中度和30例重度发育异常)。通过计数抗原阳性细胞,与正常黏膜和腺癌相比,根据免疫染色的位置、数量和强度来评估这三种蛋白的表达。p53蛋白仅在散发性(6.6%)重度发育异常病例中出现。与炎症再生性黏膜(14.8%)相比,bcl-2表达在轻度发育异常病例(61.1%)中显著更常见(p<0.005)。在轻度发育异常病例中,bcl-2阳性细胞从隐窝的下三分之一延伸至中三分之一。bcl-2表达在中度和重度发育异常阶段(75.8%)持续存在,在此阶段隐窝全长均发现抗原阳性细胞。与轻度发育异常(标记指数=16.7)相比,中度发育异常阶段(标记指数=26.3)核蛋白Ki-67表达显著增加(p<0.005),与中度发育异常相比,重度发育异常阶段(标记指数=36.7)也是如此,此时细胞增殖区域沿隐窝全长增宽。在结肠扁平黏膜上皮发育异常的发生过程中,p53基因的改变程度较低,仅在散发性重度发育异常病例中出现。bcl-2基因的突变参与病变的发生,但不参与其向癌的进展。Ki-67蛋白表达增加表明细胞增殖增加,这与上述机制一起参与了结肠扁平黏膜上皮发育异常的发生和进展过程。