期刊文献+

FOXC2在结直肠癌中的表达及意义 被引量:7

Expression of FOXC2 and its clinical pathologic significance in colorectal cancer
下载PDF
导出
摘要 目的检测FOXC2在结直肠癌(CRC)细胞和组织中的表达,探讨FOXC2的异常表达与结直肠癌发生、发展的关系及其临床意义。方法蛋白免疫印迹法和实时定量PCR法检测FOXC2在结直肠癌细胞、结直肠癌活检组织及相应癌旁正常组织中蛋白和mRNA表达水平的差异;采用免疫组化方法检测102例结直肠癌石蜡组织切片中FOXC2的表达,并分析其与结直肠癌的临床病理因素的关系。结果 FOXC2蛋白和mRNA在具有高转移潜能的HCT116和SW620结直肠癌细胞株中均高表达,在低转移潜能的HT29细胞株中低表达,且结直肠癌组织中FOXC2蛋白和mRNA表达水平显著高于正常结直肠黏膜组织;此外,FOXC2的表达水平与Dukes分期、T分期以及远处转移呈正相关性(P<0.05)。结论 FOXC2在结直肠癌中高表达,其表达水平与结直肠癌进展密切相关,可作为预测结直肠癌进展和转移的分子标记物之一。 Purpose To investigate the expression and clinicopathologic significance of FOXC2 in colorectal cancer.Methods FOXC2 protein and mRNA expression in colorectal cancer( CRC) cell lines,CRC biopsies and their matched adjacent tissues were detected by real time RT-PCR and Western blot,respectively. Immunohistochemincal analysis was used to examine the expression of FOXC2 in 102 cases of paraffin-embedded colorectal cancer tissues. Results FOXC2 protein and mRNA were highly expressed in aggressive colorectal cancer cell lines HCT116 and SW620,but relatively lower expressed in less aggressive cell line HT29. In addition,both of FOXC2 mRNA and protein expression levels were significantly higher in colorectal cancer biopsies than that in their matched adjacent tissues. FOXC2 was strongly expressed in paraffin-embedded colorectal cancer tissues. Additionally,strong expression of FOXC2 was significantly associated with Dukes stage,T classification and distant metastasis( P〈0. 05). Conclusion FOXC2 is highly expressed in colorectal cancer. High expression of FOXC2 is closely related to progression of CRC. FOXC2 may serve as a novel molecular marker for prediction of colorectal cancer progression and metastasis.
出处 《诊断病理学杂志》 CSCD 2016年第4期272-275,共4页 Chinese Journal of Diagnostic Pathology
基金 国家自然科学基金项目(81172055) 广州市珠江科技新星专项项目(2012J2200052)
关键词 结直肠癌 FOXC2 表达 分子标记物 Colorectal cancer FOXC2 Expression Biomarker
  • 相关文献

参考文献19

  • 1Siegel R,Ma J,Zou Z,et al.Cancer statistics,2014[J].CA:A Cancer J Clini,2014,64(1):9-29.
  • 2Siegel R,Desantis C,Jemal A.Colorectal cancer statistics,2014[J].CA Cancer J Clin,2014,64(2):104-117.
  • 3葛畅,王鲁平,许春伟,方园,张玉萍.结直肠锯齿状病变中p16基因甲基化状态和蛋白表达的研究[J].诊断病理学杂志,2014,21(3):169-174. 被引量:4
  • 4Bosman SJ,Vermeer TA,Dudink RL,et al.Abdominosacral resection:long-term outcome in 86 patients with locally advanced or locally recurrent rectal cancer[J].Eur J Surg Oncol,2014,40(6):699-705.
  • 5Kume T.Specification of arterial,venous,and lymphatic endothelial cells during embryonic development[J].Histol Histopathol,2010,25(5):637-646.
  • 6Gronning LM,Baillie GS,Cederberg A,et al.Reduced pde4expression and activity contributes to enhanced catecholamineinduced camp accumulation in adipocytes from foxc2 transgenic mice[J].FEBS lett,2006,580(17):4126-4130.
  • 7Kume T.Foxc2 transcription factor:A newly described regulator of angiogenesis[J].Trends Cardi Rasc Med,2008,18(6):224-228.
  • 8Ren YH,Liu KJ,Wang M,et al.De-sumoylation of foxc2 by senp3 promotes the epithelial-mesenchymal transition in gastric cancer cells[J].Oncotarget,2014,5(16):7093-7104.
  • 9Zheng CH,Quan Y,Li YY,et al.Expression of transcription factor foxc2 in cervical cancer and effects of silencing on cervical cancer cell proliferation[J].Asian Pac J Cancer Prev,2014,15(4):1589-1595.
  • 10Pietrowski D,Wiehle P,Sator M,et al.Regulation of the angiopoietin-2 gene by hcg in ovarian cancer cell line OVCAR-3[J].Hom Metab Res,2010,42(5):328-333.

二级参考文献17

  • 1杨艳芳,胡晓琴,梁小波,李佩珍.p16基因在结直肠癌中的表达及与术后生存期的关系[J].现代预防医学,2012,39(22):5911-5912. 被引量:3
  • 2Snover DC. Update on the serrated pathway to colorectal carcinoma [ J ]. Hum Pathol, 2011,42 ( 1 ) : 1 - 10.
  • 3Hamilton SR, Bosman FT, Boffetta P. Carcinoma of the colon and rectum[A]. WHO Classification of tumors of the digestive system. Pathology and genetics tumours and digestive system[ M]. 4th edi. Switzerland : WHO press, 2010. 134 - 146, 160 - 165.
  • 4Kurita S, Ohkoshi S, Yano M, et al. Progression of hypermethylation of the p16(INK4A) gene from normal liver to nontumorous liver and hepatocellular carcinoma: an evaluation using quantitative PCR analysis [ J]. Dig Dis Sci, 2009,54 (1) :80 -88.
  • 5Ogino S, Kawasaki T, Brahmandam M, et al. Precision and performance characteristics of bisnlfite conversion and real - time PCR (MethyLight) for quantitative DNA methylation analysis [J]. J Mol Diagn, 2006,8(2):209-217.
  • 6Eads CA, Lord RV, Kurumboor SK, et al. Fields of aberrant CpG island hypermethylation in Barrettb esophagus and associated adenocarcinoma [ J ]. Cancer Res, 2000,60 ( 18 ) : 5021 - 5026.
  • 7Jemal A, Siegel R, Xu J, et al. Cancer statistics, 2010[J]. CA Cancer J Clin, 2010,60(5 ) :277 - 300.
  • 8Kaji E, Uraaka T, Kato J, et al. Externalization of saw-tooth architecture in small serrated polyps implies the presence of methylation of IGFBP7[J]. Dig Dis Sci, 2012,57(5) :1261 -1270.
  • 9Jass J R, Whitehall V L, Young J, et al. Emerging concepts in colorectal neoplasia[J]. Gastroenterology, 2002,123(3) :862 -876.
  • 10Dong S M, Lee E J, Jeon E S, et al. Progressive methylation during the serrated neoplasia pathway of the colorectum[ J]. Mod Pathol, 2005,18(2) :170 - 178.

共引文献3

同被引文献65

  • 1赵俊卿,李云峰,杨之斌.肿瘤细胞发生细胞上皮-间质转变机制的研究[J].肿瘤,2010,30(10):890-893. 被引量:27
  • 2杨倩,马翔,李华驰,等.基因组学与蛋白质组学在结直肠癌研究中的进展[J].中国临床医师杂志,2013,7(3):131.
  • 3Guarino M, Rubino B, Ballabion G.The role of epithelial-mesen- chymal transition in cancer pathology [ J 1. Pathology, 2007, 39 (3) :305-318.
  • 4David JM, Rajasekaran AK. Dishonomhle discharge: The oncogenic roles ofcleaved E-cadherin fragments [ J 1. Cancer Res, 2012,2 (12) : 2917-2923.
  • 5Shimeld SM, Degnan B, Luke GN. Evolutionary genomics of the Fox genes: origin of gene families and the ancestry of gene clusters [ J ]. Genomics, 2010, 95 ( 5 ) : 256- 260.
  • 6Lindley LE, Briegel KJ. Molecular characterization of TGF beta- induced epithelial-mesenchyma] transition in normal finite lifespan human mammary epithelial cells [ J 1. Biochem Biophys Res Commun, 2010, 399(4):659-664.
  • 7Ren YH, Liu KJ, Wang M, et al. De-sumoylation of foxc2 by senp3 promotes the epithelial-mesencbymal transition in gastric cancer cell[ J ]. Oncotarget, 2014,5 (16) : 7093- 7104.
  • 8Ren YH, Liu KJ, Wang M, et al. Dc-sumoylation of foxc2 by senp3 promotesthe epithelial-mesenchymal transition in gastric cancer cells [ J ].Oncotarget, 2014,5 (16) :7093-7104.
  • 9You W, Gao H, Fan L, et al. Foxc2 regulates osteogenesis and angiogenesis of bone marrow mesenchylnal stem cells [ J ]. BMC Muscul Dis ,2013,14( 1 ) : 1235-1245.
  • 10Ye J, Wu D, Wu E, et al. The cancer stem cell niche :cross talk between cancer stem cells and their mi Tumour Biol,2014,35(5) :3945-3951.

引证文献7

二级引证文献27

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