期刊文献+

子宫内膜癌组织中DcR3的表达及临床意义

Expression and clinical significance of DcR3 in human endometrial carcinoma tissues
下载PDF
导出
摘要 目的:检测DcR3在正常增生期子宫内膜、子宫内膜非典型增生和子宫内膜癌组织中的表达,探讨它们在子宫内膜癌发生、发展中的作用。方法:用免疫组织化学法检测DcR3在不同子宫内膜组织中的表达情况。结果:DcR3在子宫内膜癌组织中的表达水平均高于子宫内膜非典型增生和增生期子宫内膜组织(P<0.01)。DcR3的表达与子宫内膜癌的临床分期和有无淋巴结转移有关(P<0.05),但与不同病理类型、组织学分级无关(P>0.05)。结论:DcR3在子宫内膜癌的发生、发展过程中可能起着重要的作用。 ObjectiveTo detect the expressions of DcR3 protein in the tissue of proliferative phase endometrium、 endometrial atypical hyperplasia and endometrial carcinoma, and to explore its clinical significance in the development of endometrial carcinoma. Methods : Immunohistochemistry was performed to detect the expressions of DcR3 in differ-ent endometrial tissue. Results: The expression level of DcR3 protein in endometrial carcinoma was significantly high-er than that in proliferative phase endometrium and endometrial atypical hyperplasia ( P 〈 0. 01 ) . The expression of DcR3 was related to the clinical stages and lymph node metastasis of endometrial carcinoma(P 〈0. 05) ,but not cor-related with pathological type and pathological grade of endometrial carcinoma( P 〉 0. 05 ) . Conclusion : DcR3 maybe plays a important role in the tumorigenesis and progress of endometrial carcinoma .
出处 《现代肿瘤医学》 CAS 2017年第17期2785-2788,共4页 Journal of Modern Oncology
基金 佛山市科技局科研课题(编号:2014AB00379)
关键词 子宫内膜癌 免疫组化 DCR3 endometrial carcinoma, immunohistochemistry, DcR3
  • 相关文献

参考文献2

二级参考文献19

  • 1沈宏伟,吴育连,彭淑牖.DcR3基因表达与肝癌细胞的凋亡及其相互关系[J].中华外科杂志,2004,42(22):1396-1397. 被引量:2
  • 2Hong-Wei Shen Shun-Liang Gao Yu-Lian Wu Shu-You Peng.Overexpression of decoy receptor 3 in hepatocellular carcinoma and its association with resistance to Fas ligand-mediated apoptosis[J].World Journal of Gastroenterology,2005,11(38):5926-5930. 被引量:29
  • 3钟智强,兰小鹏,杨湘越,李卫滨,张鲁榕,朱忠勇.DcR3基因在原发性肺癌的扩增和表达及临床意义[J].福州总医院学报,2007,14(3):166-168. 被引量:2
  • 4Jemal A, Siegel R, Ward E, et al. Cancer statistics, 2009 [ J ]. CA Cancer J Clin ,2009,59 (4) :225 - 249.
  • 5Larsen IK, SmKstuen M, Johannesen TB, et al. Data quality at the Cancer Registry of Norway : an overview of comparability, complete- ness,validity and timeliness[ J]. Eur J Cancer,2009,45 ( 7 ) : 1218 - 1231.
  • 6Pitti RM, Masters SA, Lawrence DA, et al. Genomieamp lification of a decoy receptor for fas ligand in lung and colon cancer [ J ]. Na- ture,1998,396(6712) :699 -703.
  • 7Gill RM, Hunt JS. Soluble receptor( DeR3 ) and cellular inhibitor of apoptosis - 2 ( el "AP - 2 ) protect human Cytotrophoblast cells a- gainst LIGHTmediated apoptosis[ J]. Am J Patho1,2004,165 ( 1 ) : 309 -317.
  • 8Bai C, Connolly B, Metzker ML, et al. Overexpression of M68/DcR3 in human gastrointestinal tract tumors independent of gene amplifi- cation and its location in a four- gene cluster[ J]. Proc Natl Acad Sei USA ,2000,97(3 ) : 1230 - 1235.
  • 9Ren Z,Zhu J,Gu H,et al. Decoy receptor 3 polymorphisms are not associated with the risk of esophageal cancer in a Chinese popula- tion[J]. Biomarkers,2014,5:2.
  • 10Yu W,Xu YC,Tao Y,et al. DcR3 regulates the growth and meta- static potential of SW480 colon cancer cells[ J]. Oneol Rep,2013, 30(6) :2741 -2748.

共引文献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