期刊文献+

PSMA7对A549细胞表面黏附分子表达的影响 被引量:1

Effects of PSMA7 changes on adhesion molecule expression on A549 cell
下载PDF
导出
摘要 目的探讨PSMA7表达量的变化对A549细胞表面黏附分子ICAM-1,VCAM-1和CD44表达的影响。方法采用流式细胞仪分别检测高表达PSMA7的A549细胞[pcDNA3.1(-)/PSMA7组]和低表达PSMA7的A549细胞(shPSMA7组)表面黏附分子ICAM-1,VCAM-1和CD44的表达情况。结果与高表达阴性对照组[pcDNA3.1(-)组]相比,pcDNA3.1(-)/PSMA7组的ICAM-1(t=86.325,P=0.000)和VCAM-1(t=16.337,P=0.000)的表达量均显著降低,CD44表达量则无明显变化(t=-0.545,P=0.615),而与低表达阴性对照组(shNC组)相比,shPSMA7组ICAM-1(t=-119.827,P=0.000)和VCAM-1(t=-26.68,P=0.000)表达量均显著增高,CD44表达量则无明显变化(t=-848,P=0.444)。与pcDNA3.1(-)组相比,pcDNA3.1(-)/PSMA7组穿膜侵袭细胞的数量明显减少(t=3.553,P=0.024),而shPSMA7组明显高于shNC组(t=-3.207,P=0.033)。结论高表达或干扰PSMA7可影响A549细胞表面黏附分子ICAM-1,VCAM-1的表达,提示PSMA7可能因此参与肺腺癌细胞的侵袭和转移。 To observe the effect of PSMA7 changes on adhesion molecule expression on A549 cell, flow cytometry was used to detect the expression of ICAM-1, VCAM-1 and CD44 in pcDNA3.1(-)/PSMA7 A549 cell line and shPSMA7 A549 cell line. Compared with pcDNA3.1(-) group, the expression of ICAM-1 (t=86.325, P= 0.000) and VCAM-1 (t=16.337, P=0.000) in pcDNA3.1(-)/PSMA7 group was significantly decreased, but CD44 expression (t=-0.545, P=0.615) did not change; compared with shNC group, the expression of ICAM-1 (t=-119.827, P=0.000) and VCAM-1 (t=-26.68, P=0.000) in shPSMA7 group was significantly increased, but CD44 expression (t=-848, P=0.444) did not change; compared with pcDNA3.1(-) group, the number of migrated A549 cells in pcDNA3.1(-)/PSMA7 group was significantly decreased (t=3.553,P=0.024); and compared with shNC group, migrated A549 cells of shPSMA7 group significantly increased (t=-3.207,P=0.033). In conclusion, over- and low- expression of PSMA7 maybe affect the expression of adhesion molecule ICAM-1 and VCAM-1 in A549 cell line.
出处 《免疫学杂志》 CAS CSCD 北大核心 2014年第4期288-292,共5页 Immunological Journal
基金 国家自然科学基金(81101534) 广东省科技计划项目(2010B031600307) 广东省自然科学基金(S2012010010824) 中山市科技计划项目(20113A076)
关键词 PSMA7 高表达 干扰 A549细胞 黏附分子 PSMAT Overexpression Interference A549 cells Adhesion molecule
  • 相关文献

参考文献4

二级参考文献33

  • 1叶苏娟,冯志华,朱文,蔡春季,李潞,孙丽亚,万海粟,马力,周清华.nm23-H1基因转染前后人大细胞肺癌细胞株抑制消减cDNA文库的构建[J].中国肺癌杂志,2008,11(4):482-488. 被引量:2
  • 2Sayaka Otake,Hiroaki Takeda,Shoichiro Fujishima,Tadahisa Fukui,Tomohiko Orii,Takeshi Sato,Yu Sasaki,Shoichi Nishise,Sumio Kawata.Decreased levels of plasma adiponectin associated with increased risk of colorectal cancer[J].World Journal of Gastroenterology,2010,16(10):1252-1257. 被引量:14
  • 3王蔚,孙青,韩金祥,丁彦青,韩慧霞,杨磊,翁德胜.用基因芯片研究人肺癌转移相关基因[J].临床与实验病理学杂志,2005,21(2):155-158. 被引量:3
  • 4车国卫,周清华,覃扬,王艳萍,陈小禾,朱文,孙芝琳.nm23-H1基因转染L9981肺癌细胞前后基因表达谱的变化[J].生命科学研究,2006,10(1):77-81. 被引量:3
  • 5Huang J, Kwong J, Sun EC, et al. Proteasome complex as a potential cellular target of hepatitis B virus X protein. J Virol, 1996,70 (8): 5582.
  • 6Dong J, Chen W, Welford A, et al. The proteasome alpha-subunit XAPC7 interacts specifically with Rab7 and late endosomes. J Biol Chem, 2004,279(20) :21334.
  • 7Semenza GL O2 regulated gene expression: transcriptional control of cardio respiratory physiology by HIF-1. J Appl Physiol, 2004, 96 (3):1173.
  • 8Liu X, Huang W, Li C, et al. Interaction between c-Abl and Arg tyrosine kinases and proteasome subunit PSMA7 regulates protea-some degradation. Mol Ceil, 2006,22(3) :317.
  • 9Lin HK, Altuwaijri S, Lin WJ, et al. Proteasome activity is required for androgen receptor transcriptional activity via regulation of androgen receptor nuclear transloeation and interaction with coregulators in prostate cancer cells. J Biol Chem, 2002, 277(39): 36570.
  • 10Shi YY, Wang HC, Yin YH, et al. Identification and analysis of tumour-associated antigens in hepatocellular carcinoma. Br J Cancer, 2005,92(5) :929.

共引文献18

同被引文献1

引证文献1

二级引证文献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