人胆管细胞癌的细胞动力学和形态学研究。

H Minato, Y Nakanuma
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引用次数: 6

摘要

我们研究了48例尸检或手术切除的胆管细胞癌(CCC)的细胞动力学和形态学(47例为腺癌,其余为腺鳞状细胞癌),所有这些病例都是福尔马林固定和石蜡包埋的。细胞动力学分析采用增殖细胞核抗原(PCNA)免疫染色和流式细胞术DNA分析计数嗜银核仁组织区(AgNOR)的数量。CCC去分化与AgNOR数呈正相关(高分化腺癌为2.22 +/- 0.21,中分化腺癌为3.66 +/- 0.85,低分化腺癌为4.17 +/- 0.49)。22例中、低分化腺癌的PCNA标记指数(LI)分别为24.0 +/- 2.35和26.0 +/- 4.89,高于高分化腺癌(10.8 +/- 2.14)。多数分化良好的为二倍体,而中分化至低分化的为非整倍体。这些数据表明,细胞增殖指数和核DNA分析准确反映了CCC的组织学分级。CCC沿胆道树的解剖位置与两种细胞动力学数据无关。在尸检病例中,器官和淋巴结转移的患者往往表现出更高的DNA指数和非整倍体。该研究表明,多种细胞动力学数据的结合对于评估CCC的生物学行为是有价值的,并且还支持使用小尺寸活检标本进行CCC细胞动力学的进一步研究,作为预后指标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cell kinetic and morphological studies of human cholangiocellular carcinoma.

We investigated the cell kinetics and morphologies of cholangiocellular carcinoma (CCC) using 48 autopsied or surgically resected cases (47 were adenocarcinoma and the remaining adenosquamous cell carcinoma), all of which were formalin-fixed and paraffin-embedded. Cell kinetics were analyzed by counting the number of argyrophilic nucleolar organizer regions (AgNOR) using immunostaining of proliferating cell nuclear antigens (PCNA) and flow cytometric DNA analysis. Dedifferentiation of CCC was positively correlated with AgNOR number (2.22 +/- 0.21 in well differentiated, 3.66 +/- 0.85 in moderately differentiated and 4.17 +/- 0.49 in poorly differentiated adenocarcinomas, respectively). In 22 cases, the labeling index (LI) of PCNA was higher in moderately and poorly differentiated adenocarcinomas (24.0 +/- 2.35 and 26.0 +/- 4.89, respectively) than in well differentiated ones (10.8 +/- 2.14). A majority of well differentiated ones were diploid, while aneuploidy prevailed in moderately to poorly differentiated ones. These data suggest that cell proliferative indices and nuclear DNA analysis of CCC accurately reflect their histological grading. The anatomical location of CCC along the biliary tree had no relation to either of the cell kinetic data. In autopsy cases, the patients with organ and lymph node metastases tended to show a higher DNA index and aneuploidy. This study implies that a combination of several cell kinetic data is valuable for the evaluation of the biological behaviors of CCC, and also supports further studies of cell kinetics of CCC using small-sized biopsy specimens, as a prognostic indicator.

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