期刊文献+

Snail介导的EMT在上皮性卵巢癌组织中的作用 被引量:3

Effects of Snail mediated EMT in epithelial ovarian carcinoma
下载PDF
导出
摘要 目的检测Snail、E-cadherin及Vimentin在上皮性卵巢癌组织中的表达,探讨Snail介导的上皮间质转化(EMT)在卵巢癌发生、发展及转移中的作用。方法采用免疫组化法分别检测Snail、E-cadherin、Vimentin在48例卵巢浆液性腺癌、卵巢交界性浆液性肿瘤及卵巢浆液性腺瘤中的表达,探讨EMT相关因子表达强度的相关性及与临床病理特征之间的关系。结果 (1)Snail、Vimentin在卵巢浆液性腺癌中的表达率为(68.75%/66.67%),高于卵巢交界性浆液性腺瘤的(41.67%/37.50%)及卵巢浆液性腺瘤的(25.00%/18.75%),结果均具有显著的统计学差异(P<0.05),E-cadherin在卵巢浆液性腺癌中的表达率为27.08%,低于与卵巢交界性浆液性腺瘤的54.17%及卵巢浆液性腺瘤的75.00%,结果均具有统计学差异(P<0.05)。而卵巢交界性浆液性腺瘤组与卵巢浆液性腺瘤组比较,三种蛋白的表达均无统计学差异(P>0.05)。(2)Snail、E-cadherin及Vimentin的表达高低与FIGO分期、分化级别、有无淋巴结转移及腹膜种植有关。(3)在卵巢浆液性腺癌中,Snail与Vimentin的表达呈正相关(r=0.477,P<0.05),Snail与E-cadherin的表达呈负相关(r=-0.601,P<0.05),而E-cadherin与Vimentin表达的相关性不明显(r=-0.206,P>0.05)。结论在上皮性卵巢癌组织中,Snail、Vimentin表达上调,E-cadherin表达下调,提示Snail介导的EMT可能与卵巢癌的发生、发展及浸润转移有关。 Objective To Study the effect on Snail mediated epithelial mesenchymal transition (EMT) in ovarian cancer occurrence, development and metastasis. Methods Immunohistochemical staining was detected Snail, E-cadherin,in 48 cases of ovarian serous adenocarcinoma,ovarian serous borderline tumors and ovarian serous adenomas Vimentin,investigate the correlation between the expression of EMT -related factors and the strength and relationship between clinicopathological features. Results(1)The expression of Snail,Vimentin in ovarian serous adenocarcinoma was 68.75% and 66.67%,higher than in borderline serous ovarian tumors (41.67% and 37.50) and in ovarian serous adenomas( 25.00%and 18.75%),with significant difference(P〈0.05),the expression of E-cadherin in ovarian serous adenocarcinoma of the rate of 27.08%,lower than in borderline serous ovarian tumors(54.17%) and in ovarian serous adenomas(75.00%),with significant difference(P 〈 0.05). Between the borderline ovarian serous cystadenoma and ovarian serous adenoma group,there was statistical difference in the expression of the three proteins(P &gt; 0.05).(2)The expression level of Snail and FIGO, E-cadherin and Vimentin staging,differentiation level,there was no lymph node metastasis and peritoneal implants.(3)in ovarian serous adenocarcinoma, the expression of Snail positively correlated with Vimentin (r=0.477,P 〈 0.05),the expression of Snail was negatively correlated with E-cadherin(r=-0.601,P 〈 0.05),and the expression of E-cadherin and Vimentin correlation is not obvious(r=-0.206,P〈 0.05). Conclusion In epithelial ovarian cancer,Snail,Vimentin upregulation,E-cadherin downregulation,suggesting that Snail-mediated EMT may be transferred with ovarian cancer,development and infiltration.
作者 唐青 侯建青
出处 《中国医药科学》 2014年第7期9-13,20,共6页 China Medicine And Pharmacy
关键词 SNAIL E-CADHERIN VIMENTIN 上皮性卵巢癌 上皮间质转化 Snail E-cadherin Vimentin Epithelial ovarian cancer Epithelial-mesenchymal transition
  • 相关文献

参考文献15

  • 1Lee JM, Dedhar S, Kalluri R, et al.The epithelial- mesenchymal transition: new insights in signaling, development', and disease[J].J Cell Biol,2006, 172 ( 7 ): 973-98.
  • 2Yuen HF, Chan YK, Grills C, et al.Polyomavirus enhancer activator 3 protein promotes breast can cer metastatic progression throtLgh Snail-induced epithelial mesenchymal tran sition[J].J Pathol,2011,224 ( 1 ): 78-89.
  • 3Argast GM, Krueger JS, Thomson S, et al.Inducible expression of TGF L3, Snail and ZebI recapitulates EMT in vitro and in vivo in a NSCLC model[J].Clin Exp Metastasis, 2011,28 ( 7 ): 593-614.
  • 4Vleminckx K, Vakaet L, Jr, Mareel M, et al.Genetic manipulation of E-cadherin expression by epithelial tumor cells reveals an invasion suppressor role[J].Cell, 1991,66 ($): 107-119.
  • 5Perl AK, Wilgenbus P, Dahl U, et al.A causal role for E-cadherin in the transition from adenoma to carcinoma[J]. Nature, 1998,392 ( 11 ): 190-193.
  • 6Mareel MM, Behrens J, Birchmeier W, et al.Down- regulation of E-cadherin expression in Madin Darby canine kidney ( MDCK ) cells inside tumors of nude mice[J].Int J Cancer, 1991,47 ( 9 ) : 922-928.
  • 7Cheng JC, Auersperg N, Leung PC.Inhibition of p53 represses E-cadherin expression by increasing DNA methyltransferase-1 and promoter methy/ation in serous borderline ovarian tumor cells[J]. Oncogene, 2011,30 ( 13 ) : 3930-3942.
  • 8Cheng JC, Auersperg N, Leung PC.Inhibition of p53 induces invasion of serous borderline ovarian tumor cells by accentuating PI3K/Akt-mediated suppression of E-cadherin[J].Oncogene, 2011,30 ( 1 ) : 1020-1031.
  • 9Lowy AM, Clements WM, Bishop J, et al. 13 -catenin/ wnt signaling regulates expression of the membrane type 3 matrix metalloproteinase in gastric cancer[J].Cancer Res, 2012,66 ( 9 ): 4734-4741.
  • 10Nabais S, Machado JC, Lopes C, et al.Patterns of beta- catenin expression ingastric carcinoma- clinicopathological relevance and mutation analysis[J].Int Surg Pathol, 2011, 11 (1): 1-9.

二级参考文献4

  • 1Hamilton SR, Aaltonen LA. World health organization classification of Tumours. pathology and genetics of tumours of the digestive system lyon: IARC Press, 2000. 37-67.
  • 2Greene FL, ed. AJCC Cancer Staging Manual. 6th ed. Berlin: Springer-Verlag, 2002. 50-61.
  • 3Elloul S. Snail Slug and Smad interacting protein 1 as novel parameters of disease aggressiveness in metastatic ovarian and breast carcinoma Cancer, 2005, Apr 15; 103(8):1631-1643.
  • 4Miyoshi A. Snail accelerates cancer invasion by up regulating MMP expression and is associated with poor prognosis of hepatocellular carcinoma. Br J Cancer, 2005,92(2):252-258.

共引文献8

同被引文献54

  • 1孙朝阳,李娜,周波,杨宗元,卢运萍,翁丹卉.卵巢癌细胞上皮间质转化及侵袭转移过程中microRNA-9的调控作用[J].肿瘤防治研究,2014,41(4):316-319. 被引量:3
  • 2Berx G,Staes K,van Hengel J,et al.Cloning and characterization of human invasion suppressor gene E-cadherin(CDH1)[J].Genomics,1995,26(2):281-289.
  • 3Lin Y,Dong C,Zhou BP.Epigenetic regulation of EMT:the Snail story[J].Current pharmaceutical design,2014,20(11):1698-1705.
  • 4Tiwari N,Gheldof A,Tatari M,et al.EMT as the ultimate survival mechanism of cancer cells[J].Seminars in Cancer Biology,2012,22(3):194-207.
  • 5Zhang H,Liu CY,Zha ZY,et al.TEAD transcription factors mediate the function of TAZ in cell growth and epithelial-mesenchymal transition[J].J Biol Chem,2009,284:13355-13362.
  • 6Gao J,Zhu Y,Nilsson M,et al.TGF-βisoforms induce EMT independent migration of ovarian cancer cells[J].Cancer Cell International,2014,4(1):72.
  • 7Voronkov A,Krauss S.Wnt/beta-Catenin Signaling and Small Molecule Inhibitors[J].Current Pharmaceutical Design,2013,19(4):634-664.
  • 8Arend RC,Londoo-Joshi AI,Straughn JM,et al.The Wnt/β-catenin pathway in ovarian cancer:A review[J].Gynecol Oncol,2013,131(3):772-779.
  • 9Trécul A,Morceau F,Dicato M,et al.Dietary compounds as potent inhibitors of the signal transducers and activators of transcription(STAT)3 regulatory network[J].Genes&Nutrition,2012,7(2):111-125.
  • 10Abubaker K,Luwor RB,Escalona R,et al.Targeted Disruption of the JAK2/STAT3 Pathway in Combination with Systemic Administration of Paclitaxel Inhibits the Priming of Ovarian Cancer Stem Cells Leading to a Reduced Tumor Burden[J].Front Oncol,2014,4:75.

引证文献3

二级引证文献11

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