期刊文献+

NF-κB与PCNA在人脑星形细胞瘤中的表达 被引量:1

Expression of NF-κB and PCNA in Brain Astrocytomas
下载PDF
导出
摘要 目的:探讨NF-κB与PCNA在人脑星形细胞瘤以及正常脑组织中的表达情况及其与病理分级之间的相互关系。方法:SP免疫组织化学方法检测77例不同级别的星形细胞瘤及正常脑组织标本NF-κBp65与PCNA的表达情况。结果:除了在星形细胞瘤Ⅲ、Ⅳ级之间无显著性差异外(P>0.05),PCNA在其余各级别星形细胞瘤中的表达有显著性差异(P<0.05),其阳性率随着肿瘤级别的增高而升高。尽管NF-κB的表达总体差异有显著性(P<0.01),但NF-κB在星形细胞瘤相邻各级别之间的表达无显著性差异(P>0.05),然而高度恶性组(Ⅲ~Ⅳ级)阳性率显著高于低度恶性组(Ⅰ~Ⅱ级)阳性率,二者有显著性差异(P<0.01)。结论:NF-κB异常表达可能通过PCNA影响肿瘤细胞增殖活性,免疫组织化学方法联合检测NF-κB与PCNA的表达情况能客观反映星形细胞瘤的增殖恶性程度及预后。 Objective: To evaluate the relationship between the expression of nuclear factor κB (NF-κB) and proliferating cell antigen (PCNA) and pathology grade in brain astrocytomas. Methods: The immunostaining of NF-κBp65 and PCNA in 67 astrocytomas and 10 cases of normal brain tissues were performed by Streptavidin-Peroxidase (SP) method. Results: The result showed the difference of PCNA expression between tumor grades were statistically significant (P<0.05) except those in group III and group IV (P>0.05). Generally, the positive rate of PCNA increased with tumor grade. Though total variance of NF-κB expression among tumor grades was remarkable (P<0.01), there were no significant difference among group I,II,III and IV (P>0.05). However, the positive rate of NF-κB was much higher in tumors with higher grade of malignancy than in those with lower grade of malignancy (P<0.01). Conclusion: The abnormity of NF-κB may increase cellular proliferation activity by PCNA, immunohistochemical analysis of PCNA combined with NF-κB may be useful not only in deciding the grade of malignancy but also in some prognostic value in astrocytomas.
作者 柯超 陈坚
出处 《中国肿瘤临床》 CAS CSCD 北大核心 2004年第9期493-495,共3页 Chinese Journal of Clinical Oncology
基金 湖北省科技厅科研基金资助(编号:2002AA305B08)
  • 相关文献

参考文献11

  • 1Andrey K, Andrey G, Regina S, et al. Prognostic value of tumor associated antigen immunoreactivity and apoptosis in cerebral glioblastomas: an analysis of 168 cases [J].J Glin Pathol, 1999, 52 (3): 574-580
  • 2Shubha G. Control of development and immunity by tel transcription factors in drosophila[J]. Oncogene, 1999, 18(49): 6875 -6887
  • 3Bharti AC, Aggarwal BB. Nuclear factor-kappa B and cancer: its role in prevention and therapy [J]. Biochemical Pharmacology,2002, 64(5): 883-888
  • 4Goro O, Takashi N, Kiyoshi S, et al. Inhibition of nuclear factorκ B activation confers sensitvity to tumor necrosis factor-αby impairment of cell cycle progression in human glioma cells[J].Cancer Res, 1999, 59(17): 4446~4452
  • 5Kayaselcuk F, Zorludemir S, Gumurduhu D, et al. PCNA and Ki-67 in central nervous system tumors: correlation with the histological type and grade[J].J Neurooncol, 2002, 57(2): 115- 121
  • 6Shoichi N, Kazuo W, Masanori K, et al. Aberrant nuclear factorκB activity and its participation in the growth of human malignant astrocytoma[J].J Neurosurg, 2002, 96 (5): 909-917
  • 7武忠弼 杨光华主编.中华外科病理学[M].北京:人民卫生出版社,2002.646.
  • 8Heike LP. Activator and target genes of Rel/NF-κB transcription factors[J]. Oncogene, 1999, 18(49): 6853-6866
  • 9Beatrice R, Celine G. Aberrant rel/nfκb genes and activity in human cancer[J]. Oncogene, 1999, 18(49): 6938-6947
  • 10Delphine J, Juana W, Olivier D, et al. Induction of p21waf/Cipl by TNF-α requires NF-κB activity and antagonizes apoptosis in Ewing tumor cells[J]. Oncogene, 2000, 19(1): 61 -68

共引文献545

同被引文献6

  • 1李道明,李珊珊,赵志花,任秀花,高冬玲,阎爱华.食管鳞癌组织中核转录因子κBP65蛋白及IκBα的表达[J].郑州大学学报(医学版),2004,39(6):967-970. 被引量:2
  • 2周学东.中华口腔医学年鉴(2004年卷)[M].成都:四川科学技术出版社,2005:5
  • 3Handel ML, McMorrow LB, GravaUese EM. Nuclear factor-kappa B in rheumatoid synovium [ J]. Arthritis Rheum, 1995,38(12) :1 762
  • 4Nakayama H, Ikebe T, Beppu M ,et al. High expression levels of nuclear factor K appaB, IK appaB kinase alpha and Akt kinase in squamous cell carcinoma of the oral cavity [J]. Cancer,2001,92(12) :3 037
  • 5Hellin AC,Bentire-Alj M ,Verlaet M ,et al. Roles of nucle-ar faetor-kappaB,P53, and p21/WAFI in daunomycin-induced cell cycle arrest and apoptosis[ J]. J Pharmacol Exp Ther,2000,295 ( 3 ) :870
  • 6高黎,张彦喜,石爱梅.核因子-κBp65与IκBα在口腔白斑及鳞癌中的表达[J].实用口腔医学杂志,2009,25(1):58-61. 被引量:7

引证文献1

二级引证文献2

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