期刊文献+

MR-1S在卵巢癌组织中的表达及意义

Expression of MR-1S in Ovarian Carcinoma and Its Significance
原文传递
导出
摘要 【目的】探讨s型人肌原纤维生成调节因子(MR-1S)在卵巢癌组织中的表达及意义。【方法】收集本院近三年手术治疗的120例卵巢癌患者组织(A组),同时选取60例卵巢良性肿瘤组织(B组)和50例卵巢正常组织(c组),采用荧光定量PCR法检测三组MR—ISmRNA的表达,分析其表达与其,临床分期和病理分级之间的相关性。【结果】A组、B组和C组中MR-1SmRNA表达量分别为(2.33±0.41)、(0.89±0.78)、(0.58±0.23),三组比较差异有统计学意义(P〈0.05);A组中的MR-1SmRNA表达与患者的临床分期及病理分级间不相关(P〉0.05),但上皮性癌中浆液性癌组织中的MR-1SmRNA表达量显著高于粘液性癌和内膜性癌,其差异有统计学意义(P〈O.05)。【结论】MR_1s基因在卵巢癌组织中高表达,可成为卵巢癌诊断的一个新的标志物。 [Objective]To explore the expression of human short-type myfibrillogenesis regulator-I (MR- IS) in ovarian cancer and its significance. [Methods]The tissues ~'rom 120 patients with ovarian cancer under- going surgical treatment in our hospital were collected in recent 3 years(group A). At the same time, 60 cases of benign ovarian cancer tissues(group B) and 50 cases of normal ovarian tissues(group C) were collected. Fluorescence quantitative PCR method was used to detect the expression of MR-1S mRNA. The relationship of MR-1S mRNA expression with the clinical stage and pathologic grading was analyzed. [Results]The expres- sion levels of MR-1S mRNA in group A, group B and group C were (2.33+0.41), (0.89+0.78) and (0.58 +0.23) respectively, and there was significant difference( P d0.05). MR-1S mRNA expression in group A was not associated with clinical stage and pathological grading. The expression levels of MR-1S mRNA in se- rous carcinoma of epidermal cancer were significantly higher than those in mucinous and endometrioid carcinoma, and there was significant difference( P d0.05). [Conclusion]MR-IS gene is highly expressed in ovarian cancer tissues, and it may be a new biomarker for the diagnosis of ovarian cancer.
作者 郑桂芹
出处 《医学临床研究》 CAS 2013年第5期905-907,共3页 Journal of Clinical Research
关键词 卵巢肿瘤 病理学 Ovarian Neoplasms/PA
  • 相关文献

参考文献15

  • 1饶志跃,杨国奋,蔡木炎,邓海霞,廖奕佶,谢丹.EZH2基因在卵巢癌发生发展中的作用及其临床病理意义[J].中国肿瘤临床,2010,37(23):1321-1325. 被引量:8
  • 2Cao Q. Yu J, Dhanasekaran SM, et al . Repression of E-cad-herin by the polycomb group protein EZH2 in cancer [ J].Oncogene ,2008,27(58):7274-7284.
  • 3张惜胡.临床妇科肿瘤学[M].第2版.上海:复旦大学出版社,2002:203-208.
  • 4Aoto T.Saitoh N, Sakamoto Y, et al . Polycomb group pro-tein-associated chromatin is reproduced in post-mitotic G1phase and is required for S phase progression [J]. J BiolChem,2008,283(27) :18905-18915.
  • 5Bryant RJ, Winder SJ,Cross SS, et al . The Polycomb Groupprotein EZH2 regulates actin polymerization in human pros-tate cancer cells[J]. Prostate ,2008, 68(3):255-263.
  • 6于明东,李书忠.实时荧光定量PCR法检测人骨肉瘤耐MTX细胞系中RFC、DHFR、GST-π的mRNA表达[J].中国矫形外科杂志,2009,17(11):858-861. 被引量:12
  • 7Rosa MI, Silva GD,de Azedo Simoes PW,et al . The preva-lence of human papillomavirus in ovarian cancer: a systematicreview[J], Int J Gynecol Cancer ,2013,23(3) :437-441.
  • 8Vargas-Herndndez VM. Endometriosis as a risk factor for o-varian cancer[J]. Cir Cir ,2013,81(2) :163-168.
  • 9Gupta D,Braun DP,Staren ED, et al . Longitudinal health-re-lated quality of life assessment: implications for prognosis inovarian cancer[J]. J Ovarian Res ,2013,6(1) :17.
  • 10Freitag P. Follow-up after the treatment of ovarian cancer -really without CA 125[J], Ceska Gynekol , 2012 , 77(6) : 540-542.

二级参考文献36

共引文献29

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