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非典型子宫内膜异位症的免疫标记与恶变潜能 被引量:2

The Immunophenotype and Malignant Potential of Atypical Endometriosis
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摘要 目的:了解子宫内膜异位症(EMs)、非典型子宫内膜异位症(AEMs)与子宫内膜异位相关卵巢癌(EAOC)相互的发生发展关系,探讨AEMs在EMs组病变中的角色与恶变潜能。方法:应用免疫组化方法检测82例EMs、EMs伴反应性增生、AEMs与EAOC的PTEN、p53、ki67、ER与PR的蛋白表达,分析EMs系列病变的抑癌基因、细胞增殖活性以及激素受体三方面的变化及其相互关系。结果:单纯EMs、反应性增生、AEMs与EAOC的免疫组化标记显示:随病变进展PTEN的缺失与p53的表达升高,ER/PR的表达下降,ki67的表达有明显阶段性。PTEN的缺失始自反应性增生,自AEMs开始p53表达轻度升高,ER的表达显著下降出现在EAOC,PR的表达显著下降始自反应性增生。结论:EMs-AEMs-EAOC的发生与发展是一个连续的过程,AEMs在PTEN、p53的蛋白表达、细胞增殖活性和激素受体等方面与形态学表现一致,兼具EMs的特点与肿瘤的部分特征,提示AEMs有更高的恶变潜能。 Objective :To investigate the development correlation between EMs ,AEMs and EAOC and to explore the role and malignant potential of AEMs in the serial lesions of EMs .Methods :Immunohistochemical staining was used to detect the expression of PTEN ,p53 ,ki67 ,ER and PR in 82 cases of EMs ,EMs with reactive hyperplasia ,AEMs and EAOC .Results :Immunohistochemistry results of the spectrum of EMs-AEMs-EAOC indicated :with the development of lesions ,PTEN loss and p53 expression increased ;ER and PR expression decreased ;the intensity of ki67 expression showed different staging ;PTEN loss begun from reactive hyperplasia ;increasing of p53 expression from AEMs ;de-creasing of ER expression from EAOC and PR from reactive hyperplasia .Conclusion:The development of EMs-AEMs-EAOC is a consecutive process ;histological changes and immunophenotype are conformity ;AEMs have hold some fea-tures of EMs and tumor not only in histology but also in immunophenotype .These features suggest AEMs have a rela-tively higher potential for tumorigenesis and canceration .
出处 《医学理论与实践》 2014年第15期1975-1977,共3页 The Journal of Medical Theory and Practice
关键词 非典型子宫内膜异位症 免疫表型 恶变潜能 Atypical endometriosis,Immunophenotype,Malignant potential
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参考文献9

  • 1Rouba Ali-Fehmi,Ibrahim Khalifeh,Sudeshna Bandyopadhyay,W. Dwayne Lawrence,Elvio Silva,Dezhong Liao,Fazlul H. Sarkar,Adnan R. Munkarah.Patterns of Loss of Heterozygosity at 10q23.3 and Microsatellite Instability in Endometriosis, Atypical Endometriosis, and Ovarian Carcinoma Arising in Association With Endometriosis[J].International Journal of Gynecological Pathology.2006(3)
  • 2Tomoko Akahane,Akihiko Sekizawa,Tsuyoshi Okuda,Miki Kushima,Hiroshi Saito,Takashi Okai.Disappearance of Steroid Hormone Dependency During Malignant Transformation of Ovarian Clear Cell Cancer[J].International Journal of Gynecological Pathology.2005(4)
  • 3S. Amemiya,A. Sekizawa,J. Otsuka,T. Tachikawa,H. Saito,T. Okai.Malignant transformation of endometriosis and genetic alterations of K-ras and microsatellite instability[J].International Journal of Gynecology and Obstetrics.2004(3)
  • 4Akihiko Sekizawa,Satoshi Amemiya,Junko Otsuka,Hiroshi Saito,Antonio Farina,Takashi Okai,Tetsuhiko Tachikawa.Malignant transformation of endometriosis: application of laser microdissection for analysis of genetic alterations according to pathological changes[J].Medical Electron Microscopy.2004(2)
  • 5Marcela G.del Carmen,Anne E.Smith Sehdev,Amanda NicklesFader,Marianna L.Zahurak,MichaelRichardson,John P.Fruehauf,F. J.Montz,Robert E.Bristow.Endometriosis‐associated ovarian carcinoma[J].Cancer.2003(8)
  • 6Federico Prefumo,Pier Luigi Venturini,Ezio Fulcheri.Analysis of p53 and c-erbB-2 Expression in Ovarian Endometrioid Carcinomas Arising in Endometriosis[J].International Journal of Gynecological Pathology.2003(1)
  • 7M. Er?en,S. Rakar,B. Klan?ar,K. Syrj?nen.Endometriosis-Associated Ovarian Carcinoma (EAOC): An Entity Distinct from Other Ovarian Carcinomas as Suggested by a Nested Case-Control Study[J].Gynecologic Oncology.2001(1)
  • 8Hatice Bayramo?lu,Ender Düzcan.Atypical epithelial changes and mutant p53 gene expression in ovarian endometriosis[J].Pathology Oncology Research.2001(1)
  • 9Ricardo Sainz de la Cuesta,John H. Eichhorn,Laurel W. Rice,Arlan F. Fuller, Jr,Najmosama Nikrui,Barbara A. Goff.Histologic Transformation of Benign Endometriosis to Early Epithelial Ovarian Cancer[J].Gynecologic Oncology.1996(2)

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