期刊文献+

EGFR和P53在子宫内膜癌中的表达及临床意义 被引量:2

Expression and clinical significance of EGFR and P53 in endometrial carcinoma
下载PDF
导出
摘要 目的探讨EGFR和P53在子宫内膜癌中的表达及其临床意义。方法选取2013年1月至2013年10月在我院已确诊为子宫内膜癌的手术切除蜡块标本40例,并取同期不典型增生子宫内膜和正常子宫内膜组织标本各20例,对入组的这80例患者的组织切片均采用免疫组化的方法进行EGFR和P53蛋白测定,将检测结果与相关临床因素进行统计学分析。结果1EGFR及P53在子宫内膜癌组织中的阳性表达明显高于正常增殖期子宫内膜、不典型增生子宫内膜(P<0.05)。2EGFR及P53的表达与子宫内膜癌患者的肌层浸润深度及淋巴结转移有相关性(P<0.05),而与子宫内膜癌患者的病理分期、组织学分级、患者的年龄以及患者是否绝经无相关性(P>0.05)。3EGFR和P53的表达呈正相关(Rs=0.961,P=0.002)。结论 EGFR和P53可能是内膜癌的发病机制之一,其高表达可作为判断子宫内膜癌病情进展的重要指标。联合检测EGFR和P53对子宫内膜癌的诊断及预后预测更具有意义,也为子宫内膜癌的靶向治疗提供一定的参考。 Objective To discuss the expression and significance of EGFR and P53 in endometrial cancer. Methods Collect cases of hysterectomy in our hospital between January 2013 and October 2013,and choose 40 cases of endometrial cancer tissue sections, 20 cases of patients with atypical hyperplasia endometrium tissue section and 20 cases of normal uterine endometrial bi- opsy. Eighty cases of biopsy patients enrolled underwent EGFR and P53 determination by immunohistochemical methods,the test results were analyzed. Results ① EGFR and P53 positive expression in endometrial cancer organizations are significantly higher than the normal period of endometrial proliferation, atypical hyperplasia of endometrium, the comparison between three groups was statistically significant (P〈0.05 ). ②There were correlations between the expression of EGFR and muscular infil- tration of endometrial carcinoma and lymphatic metastasis, and no correlation with clinical stage, histological grade, age and whether menopause (P〉0.05).③There was a positive correlation between the expression of EGFR and P53 in endometrial carcinoma statistically(Rs=0. 961,P=0. 002). Conclusion EGFR and P53 may be one of the pathogenesis of endometrial car- cinoma, and its high expression can be used as a judge of the important indices for endometrial cancer progression. Combined de- tection of EGFR and P53 in diagnosis of endometrial carcinoma and prognosis prediction is more meaningful,and can provide certain reference for endornetrial cancer targeted therapy.
出处 《滨州医学院学报》 2015年第4期253-256,共4页 Journal of Binzhou Medical University
关键词 子宫内膜癌 EGFR P53 免疫组化 Endometrial carcinoma, EGFR, P53, Immunohistoche-mistry
  • 相关文献

参考文献16

  • 1乐杰.妇产科学[M].7版.北京:人民卫生出版社,2009:92-99.
  • 2Nakamura JL. The epidermal growth factor receptor in malig- nant gliomas: pathogenesis and therapeutic implieations[J]. Ex- pert Opin Ther Targets, 2007,11(4) : 463-472.
  • 3Livasy CA,Reading FC, Moore DT,et al. EGFR expression and HER2/neu overexpression/amplifieation in endometrial earcino- sareoma[J]. Gyneeol Oncol, 2006,100 (1) : 101-106.
  • 4王秀芳,温实.子宫内膜癌中p53基因的表达[J].中国实用医药,2008,3(13):125-126. 被引量:2
  • 5徐澈,赖爱鸾.子宫内膜癌的分子病理学机制与研究进展[J].现代妇产科进展,2010,19(2):140-142. 被引量:4
  • 6Franklin W A,Veve R, Hirsch FR,et al. Epidermal growth factor receptor family in lung cancer and premalignancy[J]. Semin On- col,2002,29 (1) :3-14.
  • 7侯廷军,朱丽荔,陈丽蓉,徐筱杰.EGFR和4-苯胺喹唑啉类抑制剂之间相互作用模式的研究[J].化学学报,2002,60(6):1023-1028. 被引量:10
  • 8Baselga J. Why the epidermal growth factor receptor? The rati- onale for cancer therapy[J]. Oncologist, 2002,7 (S4) : 2-8.
  • 9Smaill JB,Reweastle GW,Loo JA ,et al. Tyrosine kinase inhibi- tors. 17. Irreversible inhihitors of the epidermal growth factor re- ceptor: 4-(phenylamino) quinazoline-and 4-(phenylamino) pyrido [3,2-d] pyrimidine-6-acrylamides bearing additional solubilizing funetions[J]. J Med Chem,2000,43(7) : 1380-1397.
  • 10Ohsaki Y,Tanno S,Fujita Y,et al. Epidermal growth factor re- ceptor expression correlates with poor prognosis in Endometrial carcinoma patients with p53 overexpression[J]. Oncol Rep, 2000,7(3) : 603-607.

二级参考文献26

  • 1Temkin SM, Fleming G. Current treatment of metastatic endometrial cancer[ J]. Cancer Control,2009,16:3845.
  • 2Saegusa M, Hashimura M, Kuwata T, et al. Crosstalk between NF-kappaB/p65 and beta-catenin/TCF4/p300 signalling pathways through alterations in GSK-3beta expression during trans-differentiation of endometrial carcinoma cells[ J]. J Patho1,2007 ,213 :35-45.
  • 3Achiwa Y, Hasegawa K, Udagawa Y. Regulation of the phosphatidylinositol 3-kinase-Akt and the mitogen-activated protein kinase pathways by ursolic acid in human endometrial cancer cells [ J ]. Biosci Biotechnol Biochem, 2007,71:31-37.
  • 4Koinuma K, Shitoh K, Miyakura Y, et al. Mutations of BRAF are associated with extensive hMLH1 promoter methylation in sporadic colorectal carcinomas [ J ]. Int J Cancer,2004,108:237-242.
  • 5Lee YR,Park J,Yu HN,et al. Up-regulation of PI3K/Akt signaling by 17β-estradiol through activation of estrogen receptor-α, but not estrogen receptor-β, and stimulates cell growth in breast cancer cells [J].Biochem Biophys Res Commun,2005,336 : 1221-1226.
  • 6O'Toole SA, Dunn E,Sheppard BL,et al. Oestrogen regulated gene expression in normal and malignant endometrial tissue[ J ]. Maturitas ,2005,51 : 187-198.
  • 7Doll A, Abal M, Rigau M, et al. Novel molecular profiles of endometrial cancer-new light through old windows [ J ]. J Steroid Biochem Mol Biol, 2008,108 : 221-229.
  • 8Hecht JL, Mutter GL. Molecular and pathologic aspects of endometrial carcinogenesis [ J ]. J Clin Oncol, 2006,24 : 4783-4791.
  • 9Konopka B, Janiec-Jankowska A, Czapczak D, et al. Molecular genetic defects in endometrial carcinomas:microsatellite instability, PTEN and beta-catenin ( CTNNB1 ) genes mutations [ J ]. J Cancer Res Clin Oncol,2007,133 : 361-371.
  • 10Adrienne S McCampbell, Russell R Broaddus, et al. Overexpression of the insulin-like growth factor I receptor and activation of the AKT pathway in hyperplastic endometfium [ J ]. Clin Cancer Res, 2006,12 : 6373 -6378.

共引文献266

同被引文献18

引证文献2

二级引证文献3

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