期刊文献+

上皮性卵巢癌中IRSp53的表达及其临床意义 被引量:3

Expression and clinical significance of IRSp53 in epithelial ovarian cancer
下载PDF
导出
摘要 目的探讨胰岛素受体底物p53蛋白(insulin receptor substrate p53,IRSp53)在上皮性卵巢癌(epithelial ovarian cancer,EOC)中的表达,及其与临床病理特征、预后之间的关系。方法采用免疫组化SP法和Western blot法检测不同病理类型卵巢组织中IRSp53的表达。结果 IRSp53在EOC中的阳性率为62.82%,显著高于正常卵巢(4.55%)、良性卵巢肿瘤(18.75%)及交界性卵巢肿瘤(26.67%)(P<0.05)。IRSp53在EOC中的表达与患者血清CA125水平、FIGO分期、分化程度及术后肿瘤残余直径相关(P<0.05)。IRSp53在EOC、正常卵巢、良性卵巢肿瘤和交界性卵巢肿瘤中的表达分别为1.203±0.080、0.240±0.050、0.308±0.354和0.467±0.135,差异有统计学意义(P<0.05)。IRSp53高表达的EOC患者总生存期明显低于IRSp53低表达的患者(P<0.05)。结论 IRSp53在EOC中高表达,IRSp53高表达与患者的不良预后相关,提示IRSp53可能在EOC的发生、发展中发挥重要作用。 Purpose To explore the expression of insulin receptor substrate p53 (IRSp53) in epithelial ovarian cancer (EOC) and correlation with the clinicopathologic features. Methods Immunohistoehemieal of SP and Western blot was performed to detect IRSp53 expression in ovarian tissues. Results The positive expression rate of IRSp53 in EOC (62. 82% ) was significantly higher than normal ovaries (4. 55 % ), benign ovarian tumors ( 18.75% ) and borderline ovarian tumors (26. 67% ) ( P 〈 0. 05 ). Furthermore, IRSp53 expression was associated with high serum CA125 level, advanced FIGO stage, poor grade and dissatisfied residual tumor size (P 〈 0. 05). The expression of IRSp53 in EOC, normal ovaries, benign ovarian tumors and borderline ovarian tumors was 1. 203 ± 0. 080, 0. 240 ±0. 050, 0. 308 ±0. 354, and 0. 467 ±0. 135 respectively, the difference was statistically significant (P 〈0. 05 ). The overall survival with IRSp53 overexpression was lower ( P 〈 0. 05 ). Conclusion IRSp53 overexpression is associated with an unfavorable prognostic outcome, which suggests that IRSp53 may play a crucial role in EOC invasion and metastasis.
作者 匡军 唐良萏
出处 《临床与实验病理学杂志》 CAS CSCD 北大核心 2016年第11期1219-1222,共4页 Chinese Journal of Clinical and Experimental Pathology
基金 国家自然科学基金(81372800/H1621)
关键词 卵巢肿瘤 上皮性卵巢癌 IRSp53 临床病理特征 免疫组织化学 ovarian rieoplasm epithelial ovarian cancer IRSp53 clinicopathologic characteristics immunohistochemitry
  • 相关文献

参考文献2

二级参考文献45

  • 1文萍,胡卫华,窦骏.Wnt/β-catenin信号通路在肿瘤干细胞中作用研究进展[J].中国医药生物技术,2007,2(6):455-457. 被引量:5
  • 2Ko E C, Wang X, Fen'one S. Immunotherapy of malignant diseases. Challenges and strategies [J]. Int Arch Allergy Immunol, 2003,132 (4) :294 - 309.
  • 3Ludwig J A, Weinstein J N. Biomarkers in cancer staging, prognosis and treatment selection[J]. Nat Rev Cancer,2005 ( 11 ) ,5 : 845 - 56.
  • 4Wolff A C, Hammond M E, Schwartz J N, et al. American Society of Clinical Oncology/college of American Pathologists guideline recommendations for human epidermal growth factor receptor 2 testing in breast cancer [ J ]. J Clin 0ncol,2007,25 ( 1 ) : 118 - 45.
  • 5Nakhleh R E, Grimm E E, Idowu M O, et al. Laboratory compliance with the American Society of Clinical Oncology/college of American Pathologists (ASCO/CAP) guidelines for human epidermal growth factor receptor 2 ( HER-2 ) testing : a College of American Pathologists survey of 757 laboratories [ J ]. Arch Pathol Lab Med ,2010,134 (5) :728 - 34.
  • 6Taylor C R, Levenson R M. Quantification of immunohistochemistry-issues concerning methods, utility and semiquantitative assessment Ⅱ [J]. Histopathology,2006,49(4) :411 -24.
  • 7Vogel U F. Confirmation of a low HER-2 positivity rate of breast carcinomas-limitations of immunohistochemistry and in situ hybridization[J]. Diagn Pathol,2010 ,5 :50.
  • 8A11egra C J, Jassup J M, Somerfield M R, et al. American Society of Clinical Oncology provisional clinical opinion: testing for KRAS gene mutations in patients with metastatic colorectal carcinoma to predict response to anti-epidermal growth factor receptor monoclonal antibody therapy[ J]. J Clin Oncol,2009,27 (12) :2091 - 6.
  • 9Menard S, Casalini P, Campiglio M, et al. HER-2 overexpression in various tumor types, focussing on its relationship to the development of invasive breast cancer [ J ]. Ann Oncol, 2001,12 ( S1 ) : 15-9.
  • 10JФrgensen J T. Targeted I-IER-2 treatment in advanced gastric cancer [ J ]. Oncology ,2010,78 ( 1 ) :26 - 33.

共引文献10

同被引文献10

引证文献3

二级引证文献14

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