Kim Young Hee, Kwak Kyung A, Kang Jin Seok
Department of Biomedical Laboratory Science, Namseoul University, Cheonan 330-707, Republic of Korea.
Oncol Rep. 2014 Sep;32(3):1043-9. doi: 10.3892/or.2014.3285. Epub 2014 Jun 23.
To identify preneoplastic markers for hepatocarcino-genesis, the expression levels of neighbor of Punc E11 (Nope), E-cadherin and α-fetoprotein (AFP) were investigated in carcinogen-treated embryonic cell lineages. Mouse embryonic stem cells (ESCs), hepatic progenitor cells (HPCs), and hepatocyte‑like cells (HCs) representing 0, 22, and 40 days of liver differentiation, respectively, were treated in vitro with diethylnitrosamine (DEN) at 4 doses (0, 1, 5, and 15 mM) for 24 h. The expression of Nope, E-cadherin and AFP was examined by quantitative real-time PCR, western blotting and immunocytochemistry. DEN treatment significantly increased the mRNA expression of Nope in ESCs and HPCs, and that of E-cadherin and AFP in all three cell lines, although the changes in expression were triggered by varying DEN concentrations. Immunofluorescence staining revealed that Nope was expressed at the cell membrane in ESCs and HPCs and within granules or in the cytoplasm of HCs, which was also stained by E-cadherin. DEN treatment induced Nope expression in ESCs, HPCs and HCs and caused a concomitant increase in E-cadherin expression. Although Nope expression clearly increased following tumor induction, its expression pattern changed with the developmental stage. In conclusion, we determined that Nope expression may carry prognostic significance during early hepatocarcinogenesis. Moreover, Nope expression may serve as a novel oncofetal surface marker for preneoplastic stages that are not identifiable by the commonly used marker, AFP.
为了鉴定肝癌发生的癌前标志物,研究了致癌物处理的胚胎细胞谱系中Punc E11的邻居(Nope)、E-钙黏蛋白和甲胎蛋白(AFP)的表达水平。分别代表肝脏分化0天、22天和40天的小鼠胚胎干细胞(ESCs)、肝祖细胞(HPCs)和肝细胞样细胞(HCs)在体外分别用4种剂量(0、1、5和15 mM)的二乙基亚硝胺(DEN)处理24小时。通过定量实时PCR、蛋白质印迹和免疫细胞化学检测Nope、E-钙黏蛋白和AFP的表达。DEN处理显著增加了ESCs和HPCs中Nope的mRNA表达,以及所有三种细胞系中E-钙黏蛋白和AFP的mRNA表达,尽管表达变化是由不同的DEN浓度触发的。免疫荧光染色显示,Nope在ESCs和HPCs的细胞膜上表达,在HCs的颗粒内或细胞质中表达,E-钙黏蛋白也在此处染色。DEN处理诱导了ESCs、HPCs和HCs中Nope的表达,并导致E-钙黏蛋白表达随之增加。尽管肿瘤诱导后Nope表达明显增加,但其表达模式随发育阶段而变化。总之,我们确定Nope表达在早期肝癌发生过程中可能具有预后意义。此外,Nope表达可能作为一种新的癌胚表面标志物,用于检测常用标志物AFP无法识别的癌前阶段。