Lee K T, Liu T S
Department of Surgery, Faculty of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan.
Dig Dis Sci. 2001 Oct;46(10):2166-72. doi: 10.1023/a:1011906830301.
Neoplastic transformation of epithelial cells is commonly associated with alterations in the synthesis and structures of mucin. Mucin protein epitopes and mRNA levels were frequently altered in adenocarcinomas compared to corresponding normal tissues. Clinically, hepatolithiasis has been regarded as a risk factor for cholangiocarcinoma. The aims of this study were to determine the possible alteration of mucin gene expression in stone-containing intrahepatic bile ducts and cholangiocarcinomas and to try to predict whether or not hepatolithiasis has a predisposition to development of cholangiocarcinoma. In situ hybridization with DIG-tailed oligonucleotides was performed on sections of paraffin-embedded tissues of stone-containing intrahepatic bile ducts, cholangiocarcinomas, and normal controls to identify the expression of MUC2, MUC3, MUC4, MUC5B, and MUC5AC in nonneoplastic and neoplastic biliary epithelium. The findings showed that (1) while multiple diverse mucin genes were expressed in the biliary epithelium, MUC3 and MUC5B mRNA were the main mucin genes expressed in the biliary epithelium of stone-containing intrahepatic bile ducts and normal controls; (2) absent or decreased expression of MUC2, MUC3, and MUC5B of mRNA was found in cholangiocarcinomas in contrast to nonneoplastic biliary epithelium; and (3) increased expression of MUC4 and MU5AC of mRNA was found in cholangiocarcinomas and the biliary epithelium, especially for dysplastic cells of stone-containing intrahepatic bile ducts compared with normal controls. In this study, using in situ hybridization we demonstrated that neoplastic transformation of the biliary epithelium is accompained by alterations in mucin gene expression, the altered mucin gene expression in dysplastic cells of stone-containing intrahepatic bile ducts may reflect a higher potential for malignant transformation in these cells, and it could be a precursor of cholangiocarcinoma in the presence of hepatolithiasis.
上皮细胞的肿瘤转化通常与黏蛋白合成及结构的改变相关。与相应正常组织相比,腺癌中黏蛋白蛋白表位和mRNA水平常发生改变。临床上,肝内胆管结石被视为胆管癌的一个危险因素。本研究的目的是确定含结石的肝内胆管和胆管癌中黏蛋白基因表达的可能改变,并试图预测肝内胆管结石是否易引发胆管癌。采用地高辛尾标记寡核苷酸原位杂交技术,对含结石的肝内胆管、胆管癌及正常对照的石蜡包埋组织切片进行检测,以鉴定非肿瘤性和肿瘤性胆管上皮中MUC2、MUC3、MUC4、MUC5B和MUC5AC的表达情况。研究结果显示:(1)虽然多种不同的黏蛋白基因在胆管上皮中表达,但MUC3和MUC5B mRNA是含结石的肝内胆管和正常对照的胆管上皮中表达的主要黏蛋白基因;(2)与非肿瘤性胆管上皮相比,胆管癌中MUC2、MUC3和MUC5B mRNA表达缺失或降低;(3)与正常对照相比,胆管癌及胆管上皮中,尤其是含结石肝内胆管的发育异常细胞中,MUC4和MU5AC mRNA表达增加。在本研究中,我们采用原位杂交技术证明胆管上皮的肿瘤转化伴随着黏蛋白基因表达的改变,含结石肝内胆管发育异常细胞中黏蛋白基因表达的改变可能反映了这些细胞更高的恶性转化潜能,在存在肝内胆管结石的情况下,它可能是胆管癌的前体。