期刊文献+

P33^(ING1b)在口腔鳞状细胞癌中的表达及其临床意义 被引量:1

Expression and clinical significance of P33^(ING1b) protein in oral squamous cell carcinoma
下载PDF
导出
摘要 目的:观察P33ING1b蛋白在口腔鳞状细胞癌中的表达情况,探讨其临床病理意义。方法:采用免疫组织化学ABC法,检测20例正常口腔黏膜和57例口腔鳞状细胞癌石蜡存档标本中P33ING1b的表达情况,并分析P33ING1b蛋白表达情况与患者临床病理特征的关系。结果:P33ING1b在大部分正常黏膜有表达,以细胞核为主,阳性表达率为90.00%,在口腔鳞状细胞癌中的表达以细胞核、细胞质共同着色为主,阳性表达率为24.56%,二者比较差异有显著性(P<0.05)。口腔鳞状细胞癌中淋巴结转移组阳性表达率为46.15%(12/26),淋巴结无转移组阳性表达率为6.45%(2/31),二者比较有显著性差异(P<0.05)。结论:P33ING1b蛋白在口腔鳞状细胞癌的发生发展中可能有重要的作用。其表达由细胞核转移到细胞质可能是主要机制;P33ING1b蛋白的表达与淋巴结转移有关,可以作为判断预后的一个潜在生物学标志。 Objective:To study the expression and clinical significance of P33^ING1b protein in oral squamous cell carcinoma(OSCC). Methods: ABC imnmnohistochemical method was used to investigate the expression of P33^ING1b protein in paraffin blocks of 20 cases of normal oral mucosa and 57 of OSCC. The relationship between P33^ING1b expression and clinical data of the patients was analyzed. Results:In normal oral mucosa P33^ING1b protein was observed mostly in cell nuclear, but in OSCC in cell nuclear and cytoplasm. P33^ING1b was expressed in 90.00% of the cases of normal mucosa and 24, 56% of OSCC( P 〈 0.05 ). The positive rate of P33^ING1b protein expression was 46. 15% (12/26) in lymph node metastasis group and 6.45% (2/31) in non-metastasis group( P 〈 0.05). The P33^ING1b protein expression was not correlated witb gender, age, as well as tumor location (P 〉 0.05). Conclusions:The P33^ING1b may play an important role in the tumorgenesis and development of OSCC,one of the mechanism most probably is the translocation of the protein from nuclear to cytoplasm.
出处 《实用口腔医学杂志》 CAS CSCD 北大核心 2006年第6期811-813,共3页 Journal of Practical Stomatology
基金 河北省科技攻关计划资助项目(编号052761632)
关键词 P33^ING1B 口腔 鳞状细胞癌 免疫组织化学 分化程度 转移 P33^ING1b, Protein Mouth Squamous cell carcinoma Immunohistochemistry Differentiation Metastasis
  • 相关文献

参考文献7

  • 1Garkavtsev I,Kazarov A,Gudkov A,et al.Suppression of the noval growth inhibitor p33ING1 promototes neoplastic transformation.Nat Genet,1996,14(4):415 被引量:1
  • 2Helbing CC,Veillette C,Riabowol K,et al.A noval candidate tumour suppressor gene,ING1,is involved in the regulation of apoptosis.Cancer Res,1997,57(7):1255 被引量:1
  • 3Garkavtsev I,Riabowol K.Extension of the replicative life span of human diploid fibroblasts by inhibition of the p33ING1 candidate tumor suppressor.Mol Cel Biol,1997,17(4):2014 被引量:1
  • 4Garkavtsev I Grigorian IA,Ossovskaya VS,et al.The candidate tumour suppressor p33ING1 cooperate with p53 in cell growth control.Nature,1998,391(6664):295 被引量:1
  • 5王自强,蔡志民,余佩武.大肠癌中抑癌基因p33/ING1 mRNA的表达及意义[J].第三军医大学学报,2001,23(3):349-351. 被引量:3
  • 6丁厚中,杨海人,李海,蔡晓凤,李良波,李才华,吴晓阳,杨栋,冷新,倪灿荣,朱明华.P33^(ING1)在胃癌组织中的表达及其意义[J].第二军医大学学报,2001,22(1):57-60. 被引量:6
  • 7贺修桃,吕建华,唐佳新,廖克军,朱明山,车世友,梅进,汪斐,罗惠珍,鲁平,毛先华,刘竹君,杨美珍,徐刚,刘迎福,贺修胜.P33^(ING1b)蛋白表达与胃癌分化程度的关系[J].中国医师杂志,2005,7(2):154-156. 被引量:1

二级参考文献6

共引文献7

同被引文献8

  • 1章烨,王雅杰,姜斌,薛春燕,王梅,李平,顾军.ING1b基因蛋白在乳腺癌组织的表达及临床意义[J].临床肿瘤学杂志,2004,9(5):452-455. 被引量:4
  • 2Garkavtsev I, Kazarov A, Gudkov K, et al. Suppresion of the novel growth inhibitor P33/ING1 promotes neoplastic transformation [J]. Nat Genet, 1996,14(3) :415 -420. 被引量:1
  • 3Garkavtsev I, Demetrick D, Riabowol K. Cellular localization and chromosome mapping of a novel candidate tumor suppressor gene (ING1) [J]. Cytogenet Cell Genet, 1997, 76(3-4) :176- 178. 被引量:1
  • 4Zeremski M, Horrigan SK, Grlgorian IA, et al. Localization of the candidate tumor suppressor gene ING1 to human chromosome 13q34 [J ]. Somat Cell Mol Genet, 1997,23 (3): 233 - 236. 被引量:1
  • 5Gunduz M, Ouchida M, Fukushima K, at el. Genomic structure of the human INGI gene and tumor-specific mutation detected in head arid neck squamous cell carcinomas [J]. Cancer Res, 2000,60(12) :3143- 3146. 被引量:1
  • 6Garkavtsev I, Grigorian LA, Ossovskaya VS, et al. The candidate tumor suppression p33/ING1 cooperates with p53 in cell growth control [J ]. Nature, 1998,391(6664) : 295 - 298. 被引量:1
  • 7Shinoura N, Muramatsu Y, Nishimura M, et al. Adenovirus- mediated transfer of p33/ING1 with p53 drastically augments apoptosis in gliomas [J ]. Cancer Res, 1999,59 (21) :5521 - 5528. 被引量:1
  • 8Cox LS. Multiple pathways control cell growth and transformation: overlapping and independent activities of p53 and p21 Cipl/WAF1/Sdil [J]. Pathol, 1997, 183(7): 134 - 140. 被引量:1

引证文献1

二级引证文献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