期刊文献+

丙酮酸激酶M2在膀胱尿路上皮癌中的表达研究及临床意义 被引量:1

Expression and Significance of Pyruvate Kinase M2 in Bladder Urothelial Carcinoma
下载PDF
导出
摘要 目的:探讨丙酮酸激酶M2(PKM2)在膀胱尿路上皮癌中的表达及其意义。方法:应用免疫组化SP法,分别检测50例膀胱尿路上皮细胞癌组织及15例正常膀胱组织中PKM2的表达,并结合临床资料进行分析。结果:PKM2在膀胱尿路上皮癌组织及正常膀胱组织中的阳性表达率分别为94.0%(47/50)和13.3%(1/15),比较差异有统计学意义(P<0.05)。随着膀胱尿路上皮癌病理分级及临床分期的增高,PKM2的表达增高,差异有统计学意义(P<0.05)。结论:PKM2在膀胱尿路上皮癌组织表达明显高于非癌组织,表明其在膀胱尿路上皮癌的发生发展中起重要作用,与膀胱尿路上皮癌的分期、转移有关。 Objective:To study the expression and significance of PKM2 in bladder urothelial carcinoma. Method:The expression of PKM2 was detected by immunohistochemistry in tissue sections from 50 cases of bladder urothelial carcinoma and 15 cases of normal bladder mucosa,and their correlation with clinical data features were analyzed.Result:The PKM2 expression rate in bladder urothelial carcinoma and normal bladder tissues were 94.0% and 13.3%,the difference was statistically significant(P〈0.05).With the increase of pathological grade and clinical stage in bladder urothelial carcinoma,the expression of PKM2 was increased,the difference was statistically significant(P〈0.05). Conclusion:The expression of PKM2 was higher in the bladder urothelial carcinoma than those in the noncancerous bladder tissue,which indicates that it may play an important role during the development of bladder urothelial carcinoma.And relationship to bladder urothelial carcinoma pathological grade,clinical stage and metastasis.
出处 《中国医学创新》 CAS 2016年第11期12-15,共4页 Medical Innovation of China
关键词 能量代谢 膀胱尿路上皮癌 丙酮酸激酶M2 免疫组化 Energy metabolism Bladder urothelial carcinoma Pyruvate kinase M2 Immunohistochemical stain
  • 相关文献

参考文献19

  • 1那彦群,叶章群,孙颖浩,等主编.中国泌尿外科疾病诊断治疗指南[M].2014版.北京.人民卫生出版社,2014:217-218.
  • 2Sylvester R J, van der Meijden A P, Ooster linck W, et al.Predicting recurrence and progress ion in individual patients with stage Ta-T1 bladder cancer using EORTC risk tables: A combined analysis of 2596 patients from seven EORTC trials[J].Eur Urol, 2006, 49 ( 3 ) : 466-477.
  • 3Shelley M D, Mason M D, Kynaston H.Intravesical therapy for superficial bladder cancer: a systematic review of rand0mised trials and meta-analyses[J].Cancer Treat Rev, 2010, 36 (3) : 195-205.
  • 4Eigenbrodt E, Basenau D, Holthusen S, et al.Quantification of tumor type M2 pyruvate kinase ( Tu M2-PK ) in human carcinomas[J].Anticancer Research, 1997, 17 (4B) : 3153- 3156.
  • 5詹成,时雨,王群.丙酮酸激酶M2型应用于肿瘤诊断与治疗的研究进展[J].中华肿瘤防治杂志,2013,20(13):1043-1046. 被引量:10
  • 6Mazurek S.Pyruvate kinase type M2: A key regulator of the metabo|ic budget system in tumor cells[J].International Journal of Biochemistry & Cell Biology, 2011, 43 ( 7 ) : 969-980.
  • 7Bayley J P, Devilee P.The Warburg effect in 2012 [J].Curr OpinOncol, 2012, 24 ( 1 ) : 62-67.
  • 8Clower C V, Chatterjee D, Wang Z, et al.The alternative splicing repressors hnRNP A1/A2 and PTB influence pyruvate kinase isoform expression and cell metabolism[J].Proc Natl Acad Sci USA, 2010, 107 (5) : 1894-1899.
  • 9Mazurek S, Bosehek C B, Hugo F, et al.Pyruvate kinase type M2 and its role in tumor growth and spreading[J].Semin Cancer Biol, 2005, 15 (4) : 300-308.
  • 10Bluemlein K, Grtining N M, Feichtinger R G, et al.No evidence for a shift in pyruvate kinase PKM 1 to PKM2 expression during tumorigenesis[J].Oncotarget, 2011, 2 (5): 393-400.

二级参考文献2

共引文献18

同被引文献3

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