期刊文献+

TGF-β1对肝癌细胞系Hep3B中干性相关基因表达的影响

The Effect of TGF-β1 on Gene Expression Related to Stemness on Liver Cell Line Hep3B
下载PDF
导出
摘要 有研究表明TGF-β1可以诱导诸多上皮来源的癌细胞和正常细胞发生EMT并使其功能发生改变。实验就TGF-β1对肝癌细胞系Hep3B的作用展开研究:通过CCK8检测TGF-β1对Hep3B细胞增殖的影响,RT-PCR实验检测TGF-β1处理后细胞中EMT及干性相关基因的表达变化。结果表明:TGF-β1对Hep3B细胞的增殖无抑制作用;TGF-β1处理Hep3B细胞6d后EMT相关基因的mRNA表达水平并无显著改变,但TGF-β1可上调Hep3B细胞干性基因Oct-4,Klf-4,Nanog,C-myc的表达,并下调分化基因albumin的表达。结果提示TGF-β1一定程度上影响肝癌细胞系的干性基因表达,但并不一定是以发生EMT为前提的。 Studies have shown that TGF-β1 can induce the source of many cancer cells and normal epithelial cells place EMT, and its function changes. This study is TGF-β1 on the role of hepatocellular carcinoma cell line Hep3B. The authors detect the TGF-β influence on Hep3B cell proliferation by CCKS, as Hep3B with TGF-β1 treatment for six days, and detect the gene experssion proflie that related to EMT and stemness by qRT-PCR. The results show that. TGF-β1 has no inhibitory effect on the proliferation of Hep3B cells; Hep3B cells experience TGF-β1 treat after having no significant change in their EMT gene experssion, but TGF-β1 up-regulates Hep3B cells stem-related gene expression, and down their differentiation genes expression. This suggests that TGF-β1 to a certain extent affects the liver stem cell line gene expression, but not necessarily the prerequisite for EMT to occur.
出处 《浙江理工大学学报(自然科学版)》 2012年第1期125-128,共4页 Journal of Zhejiang Sci-Tech University(Natural Sciences)
基金 国家973基金资助项目(2010CB529406)
关键词 TGF-Β1 HEP3B EMT 干性基因 TGF-betal Hep3B EMT stem cell gene
  • 相关文献

参考文献9

  • 1Roberts A B, Wakefield L M. The two faces of trans- forming growth factor-β in carcinogenesis[J]. PNAS, 2003, 100(6): 8621-8631. 被引量:1
  • 2Gotzmann J. Hepatocytes convert to a fibroblastoid phe- notype through the cooperation of TGF-β1 and Ha-Ras steps towards invasiveness[J]. Mutation Research/Re- views in Mutation Research, 2004, 566(1): 9-20. 被引量:1
  • 3Sendural A, Guo Wenjun. The epithelial-mesenchymal transition generates cells with properties of stem cells [J]. Cell, 2008, 133(5): 704-715. 被引量:1
  • 4Hiroaki, Ikushima, Tomoki Todo, et al. Autocrine TGF-β signaling maintains tumorigenicity of glioma-Ini- tiating cells through sry-related HMG-Box factors[J]. Cell Stem Cell, 2009, 5(7): 504-514. 被引量:1
  • 5You Hanning, Ding Wei, Bart R C. Epigenetic regula- tion of cancer stem cell marker CD133 by transforming growth factor-β[J]. Hepatalogy, 2010, 49 (5): 1635- 1645. 被引量:1
  • 6Thiery, Paul Jean. Epithelial-mesenchymal transitions in turnout progression[J]. Curr Opin Cell Biol, 2003, 15(6) : 740-746. 被引量:1
  • 7Wu X Z, Chen D. Origin of hepatocellular carcinoma: role of stem cells[J]. Gastroenterol Hepatol, 2006, 21 (7) ; 1093-1098. 被引量:1
  • 8Li C, Heidt D G, Dalerba P, et al. Identification of pan- croatie cancer stem cells[J]. Cancer Res, 2007, 67(3):1030-1037. 被引量:1
  • 9Bolos V, Peinado H. The transcription factor slug re- presses E-cadherin expression and induces epithelial to mesenchymat transitions: a comparison wit h Snail and E47 repressors[J]. Cell Sci, 2003, 34(7): 499-511. 被引量:1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部