期刊文献+

E2F-1和p21^(WAF1/CIP1)在良恶性多形性腺瘤中的定量表达和意义 被引量:1

Quantitive expression and significance of E2F-1 and p21^(WAF1/CIP1) in pleomorphic adenoma and malignant pleomorphic adenoma
下载PDF
导出
摘要 目的 研究E2F - 1和 p2 1WAF1/CIP1在良、恶性多形性腺瘤中的表达和意义。方法 实验分为正常组、多形性腺瘤组 (PA)和恶性多形性腺瘤组 (MPA)。利用免疫组化和原位杂交的方法对三组分别进行E2F - 1和p2 1WAF1/CIP1的染色 ,并进行灰度值测量和统计学分析。结果 E2F - 1主要表达在肿瘤性上皮组织 ,软骨样细胞和粘液样组织中也有少量表达。在MPA组中的表达显著高于PA组 ,二者与正常组之间也有显著性差异。P2 1WAF1/CIP1主要在腺管状结构、上皮条索和团块鳞状化生结构的细胞浆中表达 ,在PA和MPA组中的表达均较弱 ,但MPA组比PA组更弱。结论 E2F - 1和p2 Objective To study the expression and significance of E2F-1 and p21 WAF1/CIP1 in the pathogenesis of pleomorphic adenoma and malignant pleomorphic adenoma.Methods Samples were divided into normal group, pleomorphic adenoma (PA) and malignant pleomorphic adenoma group (MPA). E2F-1 protein and p21 WAF1/CIP1 mRNA were stained by immunohistochemistry and in situ hybridization separately. The grey values were measured by image analysis system and analyzed by statistic method.Results Positive signals of E2F-1 were mainly found in neoplastic epithelium. E2F-1 was also expressed in chondroid and myxiod areas. Expression of E2F-1 was much higher in group MPA than in group PA. There was also a significant difference between normal group and group PA, MPA (P< 0.05). Staining of p 21WAF1/CIP1 appeared in ductlike spaces, strands epithelium and squamous epithelial cells. Staining of p21 WAF1/CIP1 was weak in group PA and MPA. However, Expression of p21WAF1/CIP1 was much weaker in group MPA than in PA group(P< 0.05). Conclusion E2F-1 and p21 WAF1/CIP1 can be useful indicators to evaluate the degree of malignance of pleomorphic adenoma.
出处 《现代口腔医学杂志》 CAS CSCD 2004年第5期406-408,共3页 Journal of Modern Stomatology
关键词 P21^WAF1/CIP1 多形性腺瘤 定量表达 恶性 正常 MPA 细胞 粘液 上皮 软骨 Pleomorphic adenoma Malignant Cell cycle
  • 相关文献

参考文献1

  • 1[美]萨姆布鲁克(Sambrook,J·)等 著,金冬雁等.分子克隆实验指南[M]科学出版社,1992.

同被引文献6

  • 1于世风.口腔组织病理学[M].5版.北京:人民卫生出版社,2003:282.
  • 2Serrano M, Hannom GJ, Beach D. A new regulatory motif in cell-cycle control causing specific inhibition of cyclin D/ CDK4 [ J ]. Nature, 1993,336 ( 6456 ) :704 - 707.
  • 3Ewen ME, Sluss HK, Sherr C J, et al. Functional interaction of the retinoblastoma protein with mammalian D-type cyclins[J]. Cell, 1993,73(3): 487 -497.
  • 4Xiong Y, Menninger J, Beach D, et al. Molecular cloning and chromosomal mapping of CCND genes encoding human D-type cyclins [ J ]. Genomics, 1992, 13 (3) :575 - 584.
  • 5I~yer P, Trembley JH, Katona R, et al. Role of CDK/cyclin complexes in transcription and RNA splicing [ J]. Cell Signal, 2005,17(9) : 1033 - 1051.
  • 6Tashiro E, Tsuchiya A, Imoto M. Functions of cyclin D1 as an oncogene and regulation of cyclin D1 expression [ J ]. Cancer Sci, 2007, 98(5) :629 -635.

引证文献1

二级引证文献3

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