期刊文献+

FSCN1与Vimentin在结肠癌中的表达与意义

Expression and significance of FSCN1 and Vimentin in colon cancer
下载PDF
导出
摘要 目的探讨FSCN1与Vimentin在人结肠癌中的表达与意义。方法采用免疫组化方法检测人结肠癌及癌旁组织中FSCN1与Vimentin的表达情况,并分析二者在结肠癌中的表达情况与临床病理参数的关系及二者表达的相关性。进一步检测人结肠癌SW-480细胞中FSCN1与Vimentin的调控关系,并研究FSCN1与人结肠癌细胞侵袭转移的关系。结果FSCN1、Vimentin在结肠癌组织中的表达均显著高于癌旁组织(P<0.001)。结肠癌中FSCN1与Vimentin表达呈显著正相关,FSCN1、Vimentin在结肠癌组织中的表达均与TNM分期、淋巴结转移、分化程度均呈正相关(P<0.001)。敲低SW-480细胞中的FSCN1后,VimentinmRNA与蛋白表达水平明显降低(P<0.05)。FSCN1干扰后,SW-480细胞的侵袭、迁移能力明显降低(P<0.05)。结论FSCN1、Vimentin在结肠癌组织中呈高表达,并均与结肠癌转移有关。FSCN1对Vimentin具有正向调控作用,FSCN1可能参与结肠癌细胞EMT过程进而调节结肠癌的转移。 Objective To investigate the expression and value of FSCN1 and Vimentin in human colon cancer.Methods The expression of FSCN1 and Vimentin were detected by immunohistochemical staining in colon cancer and adjacent tissues,and the expression of FSCN1 and Vimen-tin and clinicopathological parameters was analyzed.Furthermore,the regulation of FSCN1 and Vimentin in human colon cancer cell line SW-480 was detected,and the relationship between FSCN1 and invasion and migration of colon cancer cells was researched by cell experiments.Results The expression of FSCN1 and Vimentin in colon cancer tissues were significantly higher than those in adjacent tissues(P<0.001).The expression of FSCN1 and Vimentin in colon cancer was significantly positively correlated,and the expression of FSCN1 and Vimentin in colon cancer tissue was positively correlated with TNM stage,lymph node metastasis and differentiation degree(P<0.001).Knockdown of FSCN1 in SW-480 cells significantly reduced the expression of vimentin mRNA and protein(P<0.05).After the interference of FSCN1,the invasion and migration ability of SW 480 cells decreased significantly(P<0.05).Conclusion FSCN1 and Vimentin are highly expressed in colon cancer,and they are related to the metastasis of colon cancer.FSCN1 has a positive regulatory effect on Vimentin.FSCN1 may be involved in the EMT process of colon cancer cells and then regulate the metastasis of colon cancer.
作者 邱辉 QIU Hui(Department of Oncology,Xintai People's Hospital,Tai'an,Shandong,271200,China)
出处 《当代医学》 2021年第26期1-4,共4页 Contemporary Medicine
基金 泰安市科技发展计划(引导计划)(2018NS0246)。
关键词 结肠癌 FSCN1 VIMENTIN 上皮-间质转化 Colon cancer FSCN1 Vimentin EMT
  • 相关文献

参考文献3

二级参考文献28

  • 1Jawhari AU, Buda A, Jenkins M, et al. Fascin, an actin-bundling protein, modulates colonic epithelial cell invasiveness and differentiation in vitro[J]. Am J Pathol, 2003, 162(1): 69-80.
  • 2Buda A, Pignatelli M. Cytoskeletal network in colon cancer: from genes to clinical application[J]. Int J Biochem Cell Biol, 2004, 36(5): 759-65.
  • 3Ozerhan IH, Ersoz N, Onguru O, et al. Fascin expression in colorectal carcinomas[J]. Clinics (Sao Paulo), 2010, 65(2): 157-164.
  • 4Hashimoto Y, Skacel M, Adams JC. Association of loss of epithelial syndecan-1 with stage and local metastasis of colorectal adenocarcinomas: an study of clinically annotated tmnors[J]. BMC Cancer, 2008, 8:185.
  • 5Sato J, Fujiwara M, Kawakami T, et al. Fascin expression in dendritic cells and tumor epithelium in thymoma and thymic carcinoma [J]. Oncol Lett, 2011, 2(6): 1025-1032.
  • 6Qualtrough D, Smallwood K, Littlejohns D, et al. The actin-bundling protein fascin is overexpressed in inflammatory bowel disease and may be important in tissue repair[J]. BMC Gastroenterol, 2011, 11:14.
  • 7Gao W, Zhang C, Feng Y, et al. Fascin-1, ezrin and paxillin contribute to the malignant progression and are predictors of clinical prognosis in laryngeal squamous cell carcinoma[J]. PLoS One, 2012, 7(11): e50710.
  • 8Gun BD, Bahadir B, Bektas S, et al. Clinicopathological significance of fascin and CD44v6 expression in endometrioid carcinoma [J]. Diagn Pathol, 2012, 7:80.
  • 9Jung EJ, Lee JH, Min BW, et al, Clinicopathologic s!gnificance of fascin, extracellular matrix metalloproteinase inducer, and ezrin expressions in colorectal adenocareinoma[J]. Indian J Pathol Microbi- ol, 2011, 54(1): 32-36.
  • 10Oh SY, Kim YB, Sub KW, et al. Prognostic impact of fascin-1 expression is more significant in advanced colorectal cancer[J]. J Surg Res, 2012, 172(1): 102-108.

共引文献884

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