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Expression of epithelial cell adhesion molecule and proliferating cell nuclear antigen in diethylnitrosamine-induced hepatocarcinogenesis in mice

机译:上皮细胞粘附分子和增殖细胞核抗原在二乙基亚硝胺诱导的小鼠肝癌发生中的表达

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摘要

To clarify the role of stem cells in hepatocarcinogenesis, the expression of epithelial cell adhesion molecule (EpCAM) and proliferating cell nuclear antigen (PCNA) was investigated in mouse hepatic tumors and embryonic cell lineages. Ten ICR mice were treated with diethylnitrosamine (DEN) at 14 days of age and sacrificed at 36 weeks subsequent to DEN treatment to obtain the hepatic tumors. Mouse embryonic stem cells, hepatic progenitor cells and hepatocyte-like cells, representing 0,22 and 40 days of differentiation, respectively, were treated in vitro with DEN at four doses (0, 1, 5 and 15 mM; G1, G2, G3 and G4, respectively) for 24 h and RNA was isolated. A total of 71 hepatic tumors were obtained from the DEN-treated mice. EpCAM expression was increased mainly in hepatic tumor cells, although it was also detected in the surrounding visually normal cells. Double staining showed that EpCAM and PCNA were co-expressed in numerous tumor cells. In vitro, EpCAM expression was significantly different for G4 at day 0 (P<0.01) and for G2, G3 and G4 at day 40 (P<0.01) compared with the control (G1) at the corresponding time-point. PCNA expression was significantly different for G3 and G4 at day 0 (P<0.01), for G2, G3 and G4 at day 22 (P<0.01) and for G2 at day 40 (P<0.01) compared with G1 at the corresponding time-point. In summary, the expression of EpCAM and PCNA was increased in DEN-induced tumors and the expression of EpCAM and PCNA was altered by DEN treatment in cultured cells. T his suggests that EpCAM expression may be modulated in the progeny of adult liver stem cells during their differentiation toward hepatocytes and may be increased during DEN-induced hepatocarcinogenesis.
机译:为了阐明干细胞在肝癌发生中的作用,研究了小鼠肝肿瘤和胚胎细胞谱系中上皮细胞粘附分子(EpCAM)和增殖细胞核抗原(PCNA)的表达。将十只ICR小鼠在14天大时用二乙基亚硝胺(DEN)治疗,并在DEN治疗后36周处死以获得肝肿瘤。用DEN在四种剂量下(0、1、5和15 mM; G1,G2,G3)分别体外处理小鼠胚胎干细胞,肝祖细胞和肝细胞样细胞,分别代表0.22和40天的分化时间。和分别为G4和G4)24小时,并分离出RNA。从DEN治疗的小鼠中总共获得71个肝肿瘤。 EpCAM表达主要在肝肿瘤细胞中增加,尽管在周围的视觉正常细胞中也可以检测到。双重染色表明,EpCAM和PCNA在许多肿瘤细胞中共表达。在体外,与相应时间点的对照组(G1)相比,第0天的G4(P <0.01)和第40天的G2,G3和G4(P <0.01)的EpCAM表达显着不同。与第1天的G1相比,第3天的G3和G4的PCNA表达显着不同(P <0.01),第22天的G2,G3和G4(P <0.01)和第40天的G2(P <0.01)显着不同-点。总之,在DEN诱导的肿瘤中,EpCAM和PCNA的表达增加,并且通过DEN处理在培养细胞中改变了EpCAM和PCNA的表达。他的研究表明,EpCAM的表达可能在成年肝干细胞向肝细胞分化的过程中受到调节,并可能在DEN诱导的肝癌发生过程中增加。

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