期刊文献+

Stathmin在脑胶质瘤血管内皮细胞中的表达及意义 被引量:1

Expression and significance of Stathmin in human glioma vascular endothelial cells
原文传递
导出
摘要 目的观察Stathmin及CD105在脑胶质瘤血管内皮细胞中的表达,探讨其在脑胶质瘤血管形成中的作用。方法用SP免疫组化法检测10例正常脑组织和78例脑胶质瘤血管内皮细胞中Stathmin和CD105蛋白表达,并通过检测肿瘤微血管密度(MVD)分析肿瘤血管形成。结果正常脑组织血管内皮细胞中Stathmin和CD105均无表达.脑胶质瘤血管内皮细胞中二者均呈高表达;随着胶质瘤病理级别的增高,Stathmin和CD105表达上调,MVD值增高,Stathmin—MVD和CD105-MVD与脑胶质瘤病理分级均成正相关(r=0.912,P〈0.05;r=0.936,P〈0.05);且Stathmin—MVD和CD105-MVD之间也存在正相关(r=0.996,P〈0.05)。结论Stathmin与CD105在脑胶质瘤血管内皮细胞中均呈高表达,在肿瘤微血管形成过程起重要作用。 Objective To observe the expressions of stathmin and CD105 in human glioma vascular endothelial cells and explore their significant roles in glioma angiogenesis. Methods The protein expressions of stathmin and CD105 in the vascular endothelial cells was examined by SP immunohistochemical staining in 10 normal cerebral tissue samples and 78 cases of glioma. The microvessel density (MVD) was measured to analyze the tumor angiogenesis. Results No expression of statnmin and CD 105 was found in the normal human brain tissue; while high expression level of both stathmin and CD105 was showed in the vascular endothelial cells of glioma. The expression level of stathmin and CD105 and the value of MVD increased following the rise of the pathological grades of glioma; significant linear correlation was showed between the values of stathmin-MVD and CD105-MVD and the pathological grades of the glioma (r=0.912, P〈0.05; r=0.936, P〈0.05); stathmin-MVD and CD105-MVD were also positively correlative (r=0.996, P〈0.05). Conclusion The Stathmin and CD105 is highly expressed in the vascular endothelial cells of human glioma, suggesting its important role in the tumor angiogenesis.
出处 《中华神经医学杂志》 CAS CSCD 北大核心 2009年第12期1213-1216,共4页 Chinese Journal of Neuromedicine
关键词 STATHMIN CD105 血管内皮细胞 神经胶质瘤 Stathmin CD105 Vascular endothelial cells Glioma
  • 相关文献

参考文献14

  • 1Mistry SJ, Benham C, Atweh GF, et al. Development of ribozymes that target Stathmin, a major regulator of the mitotic spindle [J]. Antisense Nucleic Acid Drug Dev, 2001, 11 (1): 41-49.
  • 2吴晴,于颖彦,王一,朱莉菲,丁红华,陈栋晖,胡宏慧,周小寒.微血管计数和血管内皮生长因子在胃癌浸润转移中的作用[J].实用癌症杂志,2002,17(2):154-156. 被引量:6
  • 3Mistry S J, Atweh GF. Role of stathmin in the regulation of the mitotic spindle: potential applications in cancer therapy [J]. Mt Sinai J Med, 2002, 69(5): 299-330.
  • 4杨晓亮,曹卫东,章翔.14-3-3蛋白在细胞凋亡中的作用[J].中华神经外科疾病研究杂志,2008,7(1):91-93. 被引量:4
  • 5Kouzu Y, Uzawa K, Koike H, et al. Over-expression of stathmin in oral squamous-cell carcinoma correlation with turnout progression and poor prognosis[J]. Br J Cancer, 2006, 94(5): 717-723.
  • 6Chen G, Wang H, Charib TG, et al. Overexpression of oncoprotein 18 correlates with poor differentiation in lung adenocarcinomas [J]. Mol Cell Proteomies, 2003, 2(2): 107-! 16.
  • 7Alli E, Yang JM, Hait WN, et al. Silencing of stathmin induces tumor-suppressor function in breast cancer cell lines harboring mutant p53[J]. Oncogene, 2007, 26(7): 1003-1012.
  • 8Mistry SJ, Atweh GF. Therapeutic interaetions between stathmin inhibition and chemotherapeutic agents in prostate cancer[J]. Mol Cancer Ther, 2006, 5(12): 3248-3257.
  • 9Balachandran R, Welsh M J, Day BW. Altered levels and regulation of stathminin paclitaxel-resistant ovarian cancer ceils [J]. Oncogene, 2003, 22(55): 8924-8930.
  • 10范熙明,张惠中,张明华,范清宇.Stathmin基因反义核酸对人成骨肉瘤细胞系的生长抑制作用[J].第四军医大学学报,2002,23(5):469-470. 被引量:10

二级参考文献23

  • 1曹卫东,章翔,张剑宁,杨志军,甄海宁,程光,李兵,高大宽,王西玲,宋蕾,谢莉.14-3-3蛋白在人脑胶质瘤中的表达及生物学意义(英文)[J].中华神经外科疾病研究杂志,2006,5(4):292-298. 被引量:4
  • 2van Hemert MJ, Steensma HY, van Heusden GP. 14-3-3proteins: key regulators of cell division, signalling and apoptosis [J]. Bioessays, 2001, 23(10) : 936 -946.
  • 3Baxter HC, Fraser JR, Liu WG, et al. Specific 14-3-3 isoform detection and immunolocalization in prion diseases [ J ]. Biochem Soc Trans, 2002, 30(4) : 387 -391.
  • 4Fu H, Subramanian RR, Masters SC. 14-3-3 proteins: structure, function, and regulation [ J 1. Annu Rev Pharmacol Toxicol, 2000, 40 : 617 -647.
  • 5Chemik IS, Seit-Nebi AS, Marston SB, et al. Small heat shock protein Hsp20 (HspB6) as a partner of 14-3-3 gamma [J]. Mol Cell Biochem, 2007, 295(1 -2) : 9 -17.
  • 6Golubnitschaja O, Yeghiazaryan K, Skowasch D, et al. p21 (WAF1/ CIP1 ) and 14-3-3 sigma gene expression in degenerated aortic valves: A link between cell cycle checkpoints and calcification [ J ]. Amino Acids, 2006, 31(3) : 309 -316.
  • 7Heusser K, Yuan H, Neagoe I, et al. Scavenging of 14-3-3 proteins reveals their involvement in the cell-surface transport of ATP-sensitive K + channels [J]. J Cell Sci, 2006, 119(Pt 20) : 4353 -4363.
  • 8Yano M, Nakamuta S, Wu X, et al. A novel function of 14-3-3 protein: 14-3-3zeta is a heat-shock-related molecular chaperone that dissolves thermal-aggregated proteins [J]. Mol Biol Cell, 2006, 17 (11) : 4769 -4779.
  • 9Angrand PO, Segura I, Volkel P, et al. Transgenic mouse proteomics identifies new 14-3-3 associated proteins involved in cytoskeletal rearrangements and cell signaling [ J ]. Mol Cell Proteomics, 2006, 5 (12) : 2211 -2227.
  • 10Danial NN, Korsmeyer SJ. Cell death: critical control points [ J]. Cell, 2004, 116(2) : 205 -219.

共引文献16

同被引文献3

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