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DEC1基因过表达对人食管癌ECA109细胞增殖及侵袭能力的影响 被引量:4

Effect of DEC1 gene over-expression on proliferation and invasion abilities of human esophageal cancer ECA109 cells
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摘要 目的:探讨DEC1基因过表达对人食管癌ECA109细胞增殖和侵袭能力的影响及可能机制。方法:将质粒pc DNA3.1(-)/DEC1(DEC1组)和pc DNA3.1(-)(vector组)利用脂质体分别转染至人食管癌ECA109细胞中,通过real-time PCR检测转染48 h后的细胞内DEC1 mRNA表达,Western blot分别检测转染72 h后细胞内DEC1、基质金属蛋白酶9(MMP9)及细胞周期蛋白cyclin D1的蛋白表达;采用CCK-8实验、平板集落实验及Transwell实验分别检测DEC1过表达对细胞的增殖和侵袭能力的影响。结果:与vector组相比,DEC1组中DEC1的表达明显增高(P<0.01);cyclin D1和MMP9的表达明显降低(P<0.05);细胞增殖与侵袭能力明显受到抑制(P<0.01)。结论:过表达DEC1可明显抑制ECA109细胞的增殖和侵袭能力,DEC1可能通过影响MMP9和cyclin D1参与其中。 AIM:To investigate the effect of DEC1 gene over-expression on the proliferation and invasion abili-ties of human esophageal cancer ECA109 cells.METHODS: ECA109 cells were transfected with plasmid pcDNA3.1 (-)/DEC1 (DEC1 group) or pcDNA3.1 (-) (vector group).The mRNA and protein levels of DEC1, cyclin D1 and MMP-9 were evaluated by real-time PCR and Western blot, respectively.The effects of DEC1 over-expression on the prolif-eration and invasion abilities of the ECA109 cells were evaluated by CCK-8 assay, colony formation assay and Transwell test respectively.RESULTS:The DEC1 expression level in ECA109 cells in DEC1 group was significantly higher than that in vector group (P〈0.01), but the levels of MMP9 and cyclin D1 expression were opposite (P〈0.01).However, both the proliferation and invasion abilities of ECA109 cells in DEC1 groups decreased significantly as compared with those in vector group (P〈0.05).CONCLUSION:The over-expression of DEC1 significantly inhibits the proliferation and invasion of ECA109 cells, which may be involved in the expression of cyclin D1 and MMP9.
出处 《中国病理生理杂志》 CAS CSCD 北大核心 2015年第4期620-624,共5页 Chinese Journal of Pathophysiology
关键词 DEC1基因 食管癌 ECA109细胞 细胞增殖 细胞侵袭 DEC1 gene Esophageal cancer ECA109 cells Cell proliferation Cell invasion
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参考文献15

  • 1Jemal A, Bray F, Center MM, et al. Global cancer statis- ties[J1. CA Cancer J Clin, 2011 , 61(2) :69-90.
  • 2郭艳丽,郭炜,邝钢,杨植彬,董稚明.食管鳞状细胞癌中SFRP基因家族启动子区甲基化状态的检测[J].中国病理生理杂志,2011,27(2):278-283. 被引量:9
  • 3Lu P, Yang X, Huang Y , et al. Antitumor activity of a combination of rAd2p53 adenoviral gene therapy and radio- therapy in esophageal carcinoma [ J ]. Cell Biochem Bio- phys, 2011, 59(3) :147-152.
  • 4Shimada H, Ochiai T. Gene therapy for esophageal squa-mous cell carcinoma [ J ]. Front Biosci, 2008, 13 : 3364- 3372.
  • 5Peng Y, Liu W, Xiong J, et al. Down regulation of diffe- rentiated embryonic ehondrocytes 1 (DEC1) is involved in 8-methoxypsoralen-induced apoptosis in HepG2 cells [J]. Toxicology, 2012, 301 ( 1-3 ) :58-65.
  • 6Bhawal UK, Sato F, Arakawa Y, et al. Basic helix-loop- helix transcription factor DEC1 negatively regulates cyclin D1 [J]. J Pathol, 2011, 224(3):420-429.
  • 7Liu Y, Miao Y, Wang J, et al. DEC1 is positively asso- ciated with the malignant phenotype of invasive breast cancers and negatively correlated with the expression of claudin-1 [J]. Int J Mol Med, 2013, 31(4) :855-860.
  • 8Liu Y, Wang L, Lin XY, et al. The transcription factor DEC1 ( BHLHFAO/STRA13/SHARP-2 ) is negatively as- sociated with TNM stage in non-small-ceU lung cancer and inhibits the proliferation through cyclin D1 in A549 and BE1 cells [J]. Tumour Biol, 2013, 34(3):1641-1650.
  • 9Ma W, Shi X, Lu S, et al. Hypoxia-induced overexpres- sion of DEC1 is regulated by HIF-lot in hepatocellular car- cinoma[J]. Oncol Rep, 2013, 30(6):2957-2962.
  • 10Li Y, Bi Z, Yan B, et al. UVB radiation induces expres- sion of HIF-lalpha and VEGF through the EGFR/PI3K/DEC1 pathway[J]. Int J Mol Med, 2006, 18(4):713- 719.

二级参考文献32

  • 1Yamamoto H.Regulation of Wnt signaling pathway and its relationship with tumorigenesis[J].Seikagaku,2008,80(12):1079-1093.
  • 2Urakami S,Shiina H,Enokida H,et al.Combination analysis of hypermethylated Wnt-antagonist family genes as a novel epigenetic biomarker panel for bladder cancer detection[J].Clin Cancer Res,2006,12(7 Pt 1):2109-2116.
  • 3Nojima M,Suzuki H,Toyota M,et al.Frequent epigenetic inactivation of SFRP genes and constitutive activation of Wnt signaling in gastric cancer[J].Oncogene,2007,26(32):4699-4713.
  • 4Takagi H,Sasaki S,Suzuki H,et al.Frequent epigenetic inactivation of SFRP genes in hepatocellular carcinoma[J].J Gastroenterol,2008,43(5):378-389.
  • 5Bird A.Molecular biology.Methylation talk between histones and DNA[J].Science,2001,294(5549):2113-2115.
  • 6Guo W,Dong Z,He M,et al.Aberrant methylation of thrombospondin-1 and its association with reduced expression in gastric cardia adenocarcinoma[J].J Biomed Biotechnol,2010,2010:721485.
  • 7Veeck J,Niederacher D,An H,et al.Aberrant methylation of the Wnt antagonist SFRP1 in breast cancer is associated with unfavourable prognosis[J].Oncogene,2006,25(24):3479-3488.
  • 8Sogabe Y,Suzuki H,Toyota M,et al.Epigenetic inactivation of SFRP genes in oral squamous cell carcinoma[J].Int J Oncol,2008,32(6):1253-1261.
  • 9Nelson WJ,Nusse R.Convergence of Wnt,β-catenin,and cadherin pathways[J].Science,2004,303(5663):1483-1487.
  • 10Urakami S,Shiina H,Enokida H,et al.Epigenetic inactivation of Wnt inhibitory factor-1 plays an important role in bladder cancer through aberrant canonical Wnt/β-catenin signaling pathway[J].Clin Cancer Res,2006,12(2):383-391.

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