期刊文献+

p16与PCNA表达与脑胶质瘤分级的相关性及意义 被引量:7

Correlation between the expression of p16 and PCNA in grades of glioma
下载PDF
导出
摘要 目的: 研究p16 与增殖性细胞核抗原( P C N A)蛋白在各级人脑胶质瘤中的表达率及与胶质瘤病理分级的关系.方法: 利用免疫组化方法检测52 例胶质瘤手术标本中p16 与 P C N A 蛋白的表达水平,并比较二者的相关性,及其与胶质瘤病理分级的关系. 结果: 随着胶质瘤病理级别的升高p16 蛋白的表达率逐渐降低, Ⅰ~Ⅳ级阳性率分别为 75. 0% ,647% ,42.8% 和33.3% ,低度恶性组(Ⅰ~Ⅱ级)与高度恶性组(Ⅲ~Ⅳ级)有显著差异( P< 0.05). P C N A 表达强度随胶质瘤病理级别的升高而增加( P< 0.05). 所选病例的平均 P C N A 指数( P C N A L I)为 27.1, p16 与 P C N A 表达存在负相关(r= 0.485, P< 0.05). 结论: p16 及 P C N A 蛋白的表达对分析判断胶质瘤病理分级的适用性及恶性转化具有一定意义. AIM: To investigate the expression of p16 and PCNA protein in glioma and their correlation with pathological characteristics of glioma. METHODS: The expression of p16 and PCNA protein expression were observed by immunohistochemical method in 52 formalin fixed paraffin embedded glioma sections. RESULTS: Expressions of p16 protein significantly decreased with the increase of grades of glioma malignancy. The levels of p16 deletion between low malignant group(Ⅰ~Ⅱ)and high malignant group(Ⅲ~Ⅳ) were significantly different( P <0.05). Expressions of PCNA protein increased with the pathological grades of glioma( P <0.05). The mean PCNA label index (PCNA LI) was 27.1 and glioma with low PCNA LI had higher rates of p16 protein expression( P <0.05). CONCLUSION: Expressions of p16 and PCNA are of some significance in evaluating the pathological grades and biological behavior of glioma.
出处 《第四军医大学学报》 1999年第7期597-599,共3页 Journal of the Fourth Military Medical University
基金 全军"九五"科研基金
关键词 脑肿瘤 胶质瘤 P16基因 增殖细胞核抗原 glioma genes, p 16 proliferation cell nuclear antigen immunohistochemistry
  • 相关文献

参考文献22

二级参考文献65

共引文献299

同被引文献46

  • 1孙彦辉,张亚卓,王忠诚,孙梅珍,赵东海.MGMT在脑胶质瘤组织中的表达及其与患者生存期的关系[J].癌症,2004,23(9):1052-1055. 被引量:36
  • 2郭强,孙晓霞,徐亮.抑癌基因PTEN的表达与胃癌生物学行为及预后的关系[J].中国误诊学杂志,2004,4(11):1776-1778. 被引量:6
  • 3曾敬,饶慧兰,侯景辉,张萌,赵美卿,吴秋良.不同级别胶质瘤中c-kit的表达及与预后的关系[J].诊断病理学杂志,2004,11(6):448-448. 被引量:1
  • 4Li J, Yen C, Lian D, et al. PTEN, a putative protein tyrosine phos- phatase gene mutated in human brain, breast, and prostate cancer[J]. Scienee,1997,275:1943-1947.
  • 5Steck PA,Pershouse MA,Jasser SA,et al. Identification of a candi- date tumor suppressor gene, MMACI, at chromosome 10q23. 3 that is mutated in multiple advanced cancers[ J]. Nat Genet, 1997,15: 356 - 362.
  • 6Li DM ,Sun H. TEP1, encoded by a candidate tumor suppressor lo- cus,is a novel protein tyrosine phosphatase regulated by transforming growth factor 13 [ J ]. Cancer Res, 1997,57:2124 - 2129.
  • 7Taniyama K, Goodison S, L to R, et al. PTEN expression is main- tained in sporadic colorectal tumors [ J ]. J Pathol, 2001,194 ( 3 ) : 341 - 348.
  • 8Reika I,Takashi K,Yoichi A. Association of p16 homozygous dele- tions with clinicopathologic characteristics and EGFR/KRAS/p53 mutations in lung adenocarcinoma C lin[ J ]. Cancer Res,2008,14: 3746.
  • 9Alfred K,Yin L,Chung Y. Clinicopathological roles of alterations of tumor suppressor gene p16 in papillary thyroid carcinoma[ J]. Ann Surg Onco1,2007,14 : 1772.
  • 10Burd CJ,Petre CE,Moghadam H,et al. CyclinD1 binding to the an- drogen receptor (AR) NH2 - terminal domain inhibits activation function-association and reveals dual roles for AR corepression [ J ]. Mol Endocrino1,2005 ,19 :607.

引证文献7

二级引证文献46

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