期刊文献+

胃癌细胞基质金属蛋白酶-2、9的表达及对细胞迁移的影响 被引量:6

Expression of Matrix Metalloproteinase-2 and-9 and Effect on Invasion of Two Gastric Cancer Cell Lines
下载PDF
导出
摘要 目的研究基质金属蛋白酶-2、9(matrix metalloproteinase-2、9,MMP-2、9)在胃癌细胞株HGC-27和SGC-7901的表达及对细胞迁徙转移的影响。方法采用Real-time PCR检测MMP-2、9 mRNA的含量;以ELISA检测培养上清液中MMP-2、9的相对浓度;通过明胶酶谱法测定培养上清液中的MMP-2、9比活。用Transwell小室迁徙实验、同质黏附和异质黏附实验比较两株细胞体外迁徙黏附能力。结果HGC-27中MMP-2和MMP-9 mRNA含量高于SGC-7901。HGC-27上清液MMP-2、9相对浓度均高于SGC-7901,且MMP-2比活高于SGC-7901,两株细胞MMP-9比活相近。HGC-27穿膜细胞数和异质黏附细胞数高于SGC-7901,同质黏附细胞数低于SGC-7901,差异均有统计学意义(P<0.05)。结论迁徙和异质黏附能力较强、同质黏附能力较弱的胃癌细胞HGC-27的MMP-2、9表达较强,提示MMP-2、9高表达可能促进胃癌细胞迁徙转移。 Objective To compare the expression of MMP-2 and MMP-9 and explore the effects of MMP- 2 and MMP-9 on invasion and metastasis of gastric cancer cell lines HGC27 and SGC7901. Methods The mRNA levels of MMP-2 and MMP-9 were detected using Real-time PCR. Relative concentrations of MMP-2 and MMP-9 in the culture medium were measured with ELISA. Though gelatinase zymography, specific activities of MMP-2 and MMP-9 in the culture medium were analyzed. By transwells chamber model assay, the invasion abilities of two cell lines were compared, and using homogeneous adhesion and heterogeneous adhesion experiments their adhesion ability were compared. Results The level of MMP-2 and MMP-9 mRNA in HGC-27 were higher than that in SGC-7901. The relative concentrations of MMP- 2 and MMP-9 in HGC-27 culture medium were higher than that in SC,-C-7901 culture medium. The spe- cific activity of MMP-2 in HGC-27 culture medium was stronger than that in SGC-7901 medium, meanwhile, the specific activities of MMP-9 were similar in two cell lines. For HGC-27, transmembrane cell count and heterogeneous adhesion cell count were more than the SCK2-7901, and homogeneous adhesion cell count was less than SGC-7901 (P〈0. 05). Conclusion Compared with SGC-7901, the expressions of MMP-2 and MMP-9 of HGC-27 were higher, and the invasion and heterogeneity adhesion ability were stronger, but the homogeneous adhesion capacity was weaker. The results suggest that the expression of MMP-2 and MMP-9 may promote the invasion and metastasis of cancer cell.
出处 《肿瘤防治研究》 CAS CSCD 北大核心 2010年第1期12-15,共4页 Cancer Research on Prevention and Treatment
基金 宁夏自然科学基金资助项目(NZ0772) 宁夏国际科技合作计划资助项目(2005-86)
关键词 基质金属蛋白酶 胃癌细胞 迁徙 转移 Matrix metalloproteinases Gastric cancer cell Invasion Metastasis
  • 相关文献

参考文献4

二级参考文献19

  • 1Johansson N,Ahonen M,kahanv M.Matrix metalloproteinases in tumor invasion.Cell Mol Life Sci,2000;57(1):5.
  • 2Curran S,Murray GI.Matrix metalloproteinases in tumor invasion and metastasis.J Pathol,1999;189(3):300.
  • 3Talvensaari A,Apaja-Sarkkinen M,Hiyhtya M, et al.Martrix Metalloproteinases 2 immunoactive Protein Appears Early in Cervical Epithelial Dedifferentiation.Gynecol Oncol,1999;72:306.
  • 4Kawano N,Osawa H, Ito T, et al.Expression of Gelatinase A,Tissue Inhibitor of Metalloproteinases-2,Matrilysin,and Trypsin(ogen) in Lung Neoplasms: An Immunohistochemical Study. Human Pathol,1997;28(5):614.
  • 5Davidson B,Goldberg I,Kopoloric J,et al.Expresssion of matrix metalloproteinase-9 in squamous cell carcinoma of the uterine cervix-clinicopathologic study using immunohistochemistry and mRNA in situ hybridization.Gynecol Oncol,1999;72:380.
  • 6Davidson B, Goldberg I, Kopolovic J, et al.MMP-2 and TIMP-2 expression correlates with poor prognosis in cervical carcinoma-a clinicopathologic study using immunohistochemistry and mRNA in situ hybridization.Gynecol Oncol,1999;73:372.
  • 7Jones JL, Glynn P, Walker RA, Expression of MMP-2 and MMP-9, their inhibitors, and the activitor MT1-MMP in primary breast carcinomas. J Pathol,1999;189(2):161.
  • 8Yurchenco PD,Schittny JC.Molecular architecture of basement membranes[J].FASEB J,1990,4(6):1577.
  • 9Curran S,Murray GJ.Matrix metalloproteinases in tumor invasion and metastasis[J].J Pathol,1999,189(3):300.
  • 10Nagase H,Barrett AJ,Woessner JF.Nomenclature and glossary of the matrix metalloproteinase[J].Matrix Supl,1992,1(1):421.

共引文献58

同被引文献80

  • 1陈谦学,王军民,吴立权,刘刚,黄乔春,邵步云.基质金属蛋白酶及其抑制剂在边缘系统胶质瘤侵袭中的作用[J].肿瘤防治研究,2005,32(6):336-338. 被引量:2
  • 2金东岭,时志民,田珂.乳腺癌中cyclinD2、CDK4的表达及其临床意义[J].肿瘤防治研究,2005,32(8):481-483. 被引量:6
  • 3黄金玲,蔡横,顾武军.加味小陷胸汤抗肿瘤作用的实验研究[J].中国中医药科技,2007,14(4):251-252. 被引量:13
  • 4Shaw JP, Utz PJ, Durand DB, Toole JJ, Emmel EA, Crabtree GR. Identification of a putative regulator of early T cell activation genes [J]. Science, 1988, 241(4862): 202-205.
  • 5Hogan PG, Chen L, Nardone J, Rao A. Transcriptional regulation by calcium, calcineurin, and NFAT [ J]. Genes Dev, 2003, 17 (18) : 2205-2232.
  • 6Crabtree GR, Olson EN. NFAT signaling: Choreographing the social lives of cells [ J]. Cell, 2002, 109(Suppl 1 ) : S67-S79.
  • 7Oh-hora M, Rao A. The calcium/NFAT pathway: Role in development and function of regulatory T cells [ J]. Microbes Infect, 2009, 11 (5) : 612-619.
  • 8Chuvpilo S, Zimmer M, Kerstan A, Glockner J, Avots A, Escher C, et al. Alternative polyadenylation events contribute to the induction of NF-ATc in effector T cells [ J]. Immunity, 1999, 10 (2) : 261-269.
  • 9Fougere M, Gaudineau B, Barbier J, Guaddachi F, Feugeas JP, Auboeuf D, et al. NFA33 transcription factor inhibits breast cancer cell motility by targeting the lipocalin 2 gene [ J]. Oncogene, 2010, 29(15) : 2292-2301.
  • 10Penna A, Demuro A, Yeromin AV, Zhang SL, Safrina O, Parker I, et al. The CRAC channel consists of a tetramer formed by Stiminduced dimerization of Orai dimers [ J ]. Nature, 2008, 456 (7218) : 116-120.

引证文献6

二级引证文献30

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