肝癌细胞株中赖氨酰氧化酶的表达及其对侵袭性的影响  

Expression of LOX mRNA and its impact on invasion of hepatocelluar carcinoma cell lines

在线阅读下载全文

作  者:吴鸣宇[1] 李才营[1] 蔡兵[1] 徐明[2] 陶永辉[2] 

机构地区:[1]南京医科大学附属无锡市人民医院肝胆外科,江苏省214023 [2]江苏省血吸虫病防治研究所

出  处:《江苏医药》2013年第2期138-141,共4页Jiangsu Medical Journal

摘  要:目的检测赖氨酰氧化酶(LOX)在肝癌细胞株中的表达及对肝癌细胞株侵袭性的影响。方法采用实时定量PCR方法检测不同肝癌细胞株中LOX mRNA的表达,Transwell小室侵袭实验观察不同浓度β-氨基丙腈(BAPN)对高侵袭性细胞株SK-Hep-1细胞侵袭性的影响。结果不同细胞株HepG-2、L02、MDA-MB-231、QGY7703、SK-Hep-1、SMMC-7721中LOX mRNA相对表达量依次为3.07、1.00、1.17、0.44、6.49、0.33。LOX mRNA在高侵袭细胞株SK-Hep-1中表达明显高于其他细胞株。加入不同浓度BAPN(0、0.1、0.2、0.3μmol/L,依次为1、2、3、4组)的SK-Hep-1细胞24h后穿膜数分别为(57.33±6.02)、(41.00±3.61)、(19.67±4.04)、(13.33±2.52)个。1组与3组(P<0.05)及与4组(P<0.01)、2组与3组(P<0.05)及与4组(P<0.01)差异均有统计学意义。结论高侵袭性细胞株SK-Hep-1高表达LOX mRNA,降低其LOX活性后侵袭能力明显下降。Objective To investigate lysyl oxidase(LOX) expression and its effect on the invasion of hepatocelluar carcinoma cell lines. Methods The LOX mRNA expression was quantified in different kinds of hepatocelluar carcinoma cell lines by RT-PCR assay.The influence of different concentrations of β-aminopropionitrile(BAPN) on invasion of SK-Hep-1 cell line was quantified by Transwell cell invasion assay. Results The expressions of LOX mRNA in different cell lines of HepG-2,L02,MDA-MB-231,QGY7703,SK-Hep-1,SMMC-7721 were 3.07,1.00,1.17,0.44, 6.49,0.33,respectively. LOX mRNA expression was higher in SK-Hep-1 than that in the other cell lines.The numbers of transmembraned SK-Hep-1 cells treated with different concentrations of BAPN(0,0.1,0.2, 0.3μmol/L,named groups of 1,2,3,4) were (57.33±6.02),(41.00±3.61),(19.67±4.04),(13.33±2.52),respectively. Transmembraned cells were more in group 1 than those in group 3(P〈0.05) and group 4(P〈0.01),also transmembraned cells were more in group 2 than those in group 3(P〈0.01) and group 4(P〈0.05). Conclusion LOX mRNA is highly expressed in the invasive cell line SK-Hep-1. The ability of cell invasion is decreased by reducing the activity of LOX.

关 键 词:赖氨酰氧化酶 肝癌细胞株 

分 类 号:R735[医药卫生—肿瘤]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象