期刊文献+

RhoE在胶质瘤组织中的表达及意义 被引量:1

Expression and significance of RhoE in glioma tissue
下载PDF
导出
摘要 目的探讨RhoE蛋白在胶质瘤恶性进展中的作用以及与临床预后的关系。方法应用免疫组化法检测2例正常脑组织和37例不同病理级别人脑胶质瘤瘤组织中RhoE蛋白表达情况,评估RhoE蛋白表达与胶质瘤的病理分级及临床预后的关系。结果 RhoE蛋白在正常脑组织和胶质瘤中的免疫染色评分分别为7.00±1.00和3.32±0.372。RhoE蛋白表达与胶质瘤恶性程度呈负相关,相关系数r=-0.733。RhoE蛋白免疫染色评分小于4的胶质瘤患者生存期较短(P<0.05)。结论 RhoE在胶质瘤的发生进展中呈负调控作用,RhoE的低表达与胶质瘤临床预后较差相关,其表达情况对判断胶质瘤患者的预后有一定的参考价值。 Objective To investigate the roles of RhoE in the malignant progression of glioma and evaluate the relationship between expression of RhoE and clinical prognosis. Methods Expression of RhoE protein was assessed by immunohistochemistry in 2 normal brain tissues and 37 glioma samples of different tumor grade and was statistically analyzed in combination with the follow- up survival data of patients. Results The IRS of RhoE in normal brain tissues and glioma samples was 7.00± 1.00 and 3.32 ± 0.372 respectively. Decreasing expression of RhoE is closely correlated with increasing tumor grade of glioma ( r = -0. 733 ). The glioma patients with IRS less than 4 had significantly shorter overall survival ( P 〈 0.05 ). Conclusions Reduced expression of RhoE may take part in the development of glioma. Low expression of RhoE may correlate with poor prognosis of glioma patients and expression of RhoE maybe helpful to evaluate prognosis of glioma patients.
作者 朱明亮 袁晖
机构地区 解放军第
出处 《临床神经外科杂志》 CAS 2012年第5期266-268,共3页 Journal of Clinical Neurosurgery
关键词 RHOE 胶质瘤 免疫组织化学 预后 RhoE glioma immunohistochemistry prognosis
  • 相关文献

参考文献10

  • 1Titus B, Schwartz MA,Theodorescu D. Rho proteins in cell migration and metastasis [ J ]. Crit Rev Eukaryot Gene Expr,2005,15 : 103.
  • 2Hiromichi N, Keiji S. HA1077,a Rho kinase inhibitor, suppresses glioma-indueed angiogenesis by targeting the Rho-ROCK and the mitogen-activated protein kinase kinase/extracellular signal- regulated kinase (MEK,/ERK) signal pathways J]. Cancer Sci, 2011,102:393.
  • 3Rattan R, Giri S, Singh AK, et al. Rho/ROCK Pathway as a Target of Tumor Therapy [ J. J Neurosci Res,2006,83:243.
  • 4Riento K, Villalonga P, Garg R, et al. Function and regulation of RhoE [ J]. Biochem Soc Trans,2005 ,33 :649.
  • 5Guasch RM, Scambler P, Jones G. E, et al. RhoE Regulates Actin Cytoskeleton Organization and Cell Migration [ J]. Mol Cell Bio1,1998,18 : 4761.
  • 6Priam V, Silvia FM, Anne JR. RhoE Inhibits 4E-BP1 Phosphoryl- ation and elF4E Functionlmpairing Cap-dependent Translation [J. J Biol Chem,2009,284:35287.
  • 7Belgiovine C, Frapolli R, Bonezzi K, et al. Reduced expression of the ROCK inhibitor Rnd3 is associated with increased invasiveness and metastatic potential in mesenchymal tumor cells [ J ]. PLoS One,2010,5 : 14154.
  • 8Bektic J, Pfeil K, Berger AP. Small G-protein RhoE is under- expressed in prostate cancer and induces cell cycle arrest and apoptosis [ J ]. Prostate,2005,64:332.
  • 9Yan B, Chour HH, Peh BK, et al. RhoA protein expression correlates positively with degree of malignancy in astrocytomas [ J ]. Neurosci Lett,2006,407 : 124.
  • 10Poch E, Minambres R, Mochol E,et al. RhoE interferes with Rb inactivation and regulates the proliferation and survival of the U87 human glioblastoma cell line [ J ]. Exp Cell Res,2007,313:719.

同被引文献10

  • 1Guasch RM, Scambler P, Jones GE, et al. RhoE regulates actin cytoskeleton organization and cell migration [ J ]. Mol Cell Biol, 1998,18:4761.
  • 2Bektic J, Pfeil K, Berger AP. Small G-protein RhoE is underex- pressed in prostate cancer and induces cell cycle arrest and apoptosis [ J ]. Prostate,2005,64:332.
  • 3Klein RM, Aplin AE. Rnd3 regulation of the actin cytoskeleton promotes melanoma migration and invasive outgrowth in three dimensions[ J]. Cancer Res ,2009,69:2224.
  • 4Kanzawa T,Ito H, Kondo Y, et al. Current and future gene therapy for malignant gliomas[ J]. J Biomed Biotechnol,2003 ,3 :25.
  • 5Tamiya T, Takao S, Iehikawa T, et al. Date I : Successful chemother- apy for congenital malignant gliomas : a report of two cases [ J ]. Pediatr Neurosurg,2006,42:240.
  • 6Van Meir EG, Hadjipanayis CG, Norden AD, et al. Exciting new advances in neuro-oncology: the avenue to a cure for malignant glioma[ J]. CA Cancer J Clin ,2010,60 : 166.
  • 7Schmitz ML, dos Santos Silva MA, Baeuerle PA. Transactivation domain 2 of p65 NF-kappa B. Similarity to TA1 and phorbol ester- stimulated activity and phosphorylation in intact cells [ J ]. J Biol Chem, 1995,270 : 15576.
  • 8Karin M, Ben-Neriah Y. Phosphorylation meets ubiquitination: the control of NF- kappa B activity [ J ]. Annu Rev Immunol,2000,18:621.
  • 9Li L, Gondi CS, Dinh DH, et al. Transfection with anti-p65 intrabody suppresses invasion and angiogenesis in glioma cells by blocking nuclear factor-kappaB transcriptional activity[ J]. Clin Cancer Res, 2007,13:2178.
  • 10袁晖,朱明亮.RhoE表达上调抑制U87细胞增殖与侵袭[J].中华神经外科疾病研究杂志,2012,11(6):516-519. 被引量:1

引证文献1

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