期刊文献+

Par3蛋白在胶质瘤中的表达及其临床病理学意义

The Expression and Clinical Pathological Significances of Par3 in Glioma
下载PDF
导出
摘要 目的 检测Partitioning defective 3(Par3)蛋白在胶质瘤组织中的表达,并分析其临床病理学意义。方法 收集70例不同临床分期及不同分化程度胶质瘤组织及20例正常脑组织标本,应用免疫组化技术检测Par3蛋白的表达,并分析其与胶质瘤患者临床病理特征的相关性。结果 与正常脑组织相比,胶质瘤组织中Par3蛋白表达水平显著降低(P〈0.05)。Ⅲ~Ⅳ级胶质瘤组织中Par3蛋白的表达明显低于Ⅰ~Ⅱ级胶质瘤(P〈0.05)。Par3的表达水平与患者的年龄、性别以及病理组织学类型无显著相关性,但与胶质瘤临床分级显著相关(P=0.008)。结论 Par3蛋白在胶质瘤中呈低表达,并与胶质瘤的恶性程度密切相关。 Objective To explore the role of Par3 in the development of glioma by analysis of the expression of Par3 in glioma tissue. Methods A total of 70 cases of human glioma tissue with different clinical stages and differentiation histolog- ical types and 20 cases of normal brain tissue were selected. We detected the expression of Par3 by immunohistochemistry method, and analyzed its correlation with the clinicopathologic features of glioma patients. Results Compared with normal brain tissue, the expression of Par3 protein in glioma tissue decreased significantly (P〈0.05). The expression level of Par3 was significantly lower at stage III- IV than that at stage I - II (P〈0.05). The expression of Par3 presented no correlation with the age, sex and histological types of patients, but had significant correlation with the clinical stages of glioma (P = 0.008). Conclusion The Par3 was lowly expressed in glioma tissue and involved in the development and progression of glioma. It was closely correlated with the malignancy of human glioma.
出处 《肿瘤药学》 CAS 2015年第6期440-443,共4页 Anti-Tumor Pharmacy
关键词 胶质瘤 PAR3 侵袭 临床分期 Glioma Par3 Invasion Clinical stage
  • 相关文献

参考文献22

  • 1Kang JH,Adamson C,Novel chemotherapeutics and other therapies for treating high-grade glioma[J].Expert Opin Investig Drugs,2015,24(10):1361-1379.doi:10.1517/13543784.2015.1048332.
  • 2Wang J,Su HK,Zhao HF,et al.Progress in the application of molecular biomarkers in gliomas[J].Biochem Biophys Res Commun,2015,465(1):1-4.doi:10.1016/j.bbrc.2015.07.148.
  • 3Satoer D,Visch-Brink E,Dirven C,et al.Glioma surgery in eloquent areas:can we preserve cognition?[J].Acta Neurochir(Wien),2016,158(1):35-50.doi:10.1007/s00701-015-2601-7.
  • 4Zhao P,Li Q,Shi ZM,et al.GSK-3 p regulates tumor growth and angiogenesis in human glioma cells[J].Oncotar- get,2015,6(31):31901-31915.doi:10.I B632/oncotarget.5043.
  • 5Ramakrishna R,Pisapia D.Recent molecular advances in our understanding of glioma[J].Cureus,2015,7(7):e287. doi:10.7759/cureus.287.
  • 6Tyurikova 0,Dembitskaya Y,Yashin K,et al.Perspec- tives in Intraoperative Diagnostics of Human Gliomas[J]. Comput Math Methods Med,2015,2015:479014.doi:10.1155/2015/479014.
  • 7Rizzo D,Ruggiero A,Martini M et al.Molecular biology in pediatric high-grade glioma:impact on prognosis and treatment[J].Biomed Res Int,2015,2015:215135.doi:10.1155/2015/215135.
  • 8Reversat A,Yuseff MI7 Lankar D,et al.Polarity protein Par3 controls B-cell receptor dynamics and antigen extrac- tion at the immune synapse[J].Mol Biol Cell,2015,26(7):1273-1285.doi:10.1091/mbc.E14-09-1373.
  • 9Abu-Siniyeh A,Owen DM,Benzing C,et al.The aPKC/Par3/Par6 Polarity Complex and Membrane Order Are Functionally Interdependent in Epithelia During Vertebrate Organogenesis[J].Traffic,2015.doi:10.1111/tra.12339.
  • 10Matsui T,Watanabe T,Matsuzawa K,et al.PAR3 and aPKC regulate Golgi organization through CLASP2 phosphoryla- tion to generate cell polarity[J].Mol Biol Cell,2015,26(4):751-761.doi:10.1091/mbc.E14-09-1382.

二级参考文献3

共引文献1367

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