期刊文献+

脑膜瘤端粒酶的活性在判断复发和恶变中的价值 被引量:1

Value of Telomerase Activity of Meningiomas on Identifying Recurrence and Malignancy
下载PDF
导出
摘要 【目的】探讨端粒酶作为脑膜瘤标志物 ,在肿瘤良恶性鉴别、恶性程度评估以及预后预测等方面的意义。【方法】利用TRAP ELISA方法定量检测 6 1例 (份 )肿瘤标本端粒酶的活性 (以ΔA =A4 50 -A690 表示 ) ,结合肿瘤的分类和患者的临床资料 ,分析端粒酶活性作为肿瘤良恶性及判断预后的标记物的可行性。另取正常脑组织标本 2 0例作为对照。【结果】 30例脑膜瘤中 ,2 9例脑膜瘤均未测到端粒酶活性 ;1例端粒酶阳性 (阳性率 3 3%) ,ΔA =0 2 37;全组ΔA平均值 =0 0 49。 15例恶性脑膜瘤中 14例呈端粒酶阳性 (93%) ,ΔA =1 2 37~ 2 5 16 ;1例端粒酶阴性 ,ΔA =0 0 76 ,全组ΔA平均值 =1 6 30。 16例复发性脑膜瘤端粒酶均阳性 (10 0 %) ,ΔA =1 0 34~ 1 4 78,平均 1 2 5 5。脑膜瘤和复发性脑膜瘤、脑膜瘤和恶性脑膜瘤的端粒酶的阳性率和酶活性表达强度方面差异明显 (P分别为 <0 0 0 1、<0 0 1和 <0 0 0 0 5、<0 0 1)。 2 0例正常脑组织中未检测到端粒酶活性。【结论】端粒酶活性的激活在恶性脑膜瘤和复发性脑膜瘤中是较常见的现象。端粒酶作为肿瘤标志物 ,在脑膜瘤的良恶性鉴别、恶性程度评估、预后预测等方面具有重要的意义。 Objective To explore telomerase activity in meningiomas and its significance in tumor's classification, evaluation of malignancy and prognosis. Methods Telomerase activity of meningiomas (expressed as ΔA=A 450 -A 690 ) was detected quantitatively using telomerase polymerase enzyme linked immunoassay (TRAP-ELISA). Combining with the data, such as tumors histopathological classification and patients' clinical materials, the possibility of telomerase served as tumor marker for differentiating benign and malignant, evaluating malignancy, predicting prognosis in meningioma were discussed. Results Telomerase was only detected positively in one of 30 meningiomas(positive rate:3.3%), ΔA=0.237; average ΔA=0.049. In contrast, 14 of 15(93%) malignant meningiomas were positive for telomerase expression, average ΔA=1.630. In the 16 recurrence meningiomas, all were positive for telomerase expression, average ΔA=1.255. Positive rate for telomerase expression and average value were significant different between meningiomas and recurrent meningiomas(P<0.001 and P<0.01), and also different between meningiomas and malignant meningiomas(P<0.0005 and P<0.01). Telomerase activity was not detected in 20 normal brain tissues. Conclusion Activation of telomerase activity is a common phenomenon in malignant meningiomas. It is an important marker for differentiating benign and malignant, evaluating malignancy and predicting prognosis.
出处 《中山医科大学学报》 CSCD 北大核心 2002年第2期148-150,共3页 Academic Journal of Sun Yat-sen University of Medical Sciences
关键词 脑膜瘤 诊断 端粒酶 预后 复发 恶变 评估 meningioma/diagnosis telomerase prognosis
  • 相关文献

参考文献3

二级参考文献28

  • 1金冬雁(译),分子克隆实验指南(第2版),1996年,401-405,672-688页
  • 2Wen J M,Mol Pathol,1998年,51卷,2期,110页
  • 3Kang M K,Guo W,Park N H.Replicative senescence ofnormalhuman oralkeratinocytesisassociated withthelossoftelomerase activity withoutshorting oftelomeres. Cell Growth and Differentiation . 1998
  • 4CalifanoJ,Ahrendt SA,Meininger G,et al.Detection oftelomerase activity in oralrinses from head and neck squamouscellcancer patients. Cancer Research . 1996
  • 5Hiyama K,Hirai Y,Kyoizum S,etal.Activation oftelomerase in human lymphocytes and hematopoietu progenitorcells. JImmunol . 1995
  • 6Taylor RS,Ramirez RD,Ogoshi M,et al.Detection oftelomerase activityin malignantand nonmalignantskin conditions. Journal of Investigative Dermatology . 1996
  • 7Mao L,EINaggarAK,Fan YH,etal.Telomeraseactivityin head andnecksquamouscellcarcinomaandadjacenttissues. Cancer Research . 1996
  • 8Kannan S,Tahara H,Yokozaki H,etal.Telomeraseactivityin premalignant and malignantlesions of human oral mucosa. Cancer Epidemiology Biomarkers and Prevention . 1997
  • 9Mutirangura A,Supiyaphun P,Trirekapan S,etal.Telomerase activityinoralleukoplakia and head and necksquamouscellcarcinoma. Cancer Research . 1996
  • 10Nimmo ER,Cranston G,Allshire RC.Telomereassociatedchromosome breakageinfission yeastresultsin variegatedexpression ofadjacentgenes. EMBO Journal . 1994

共引文献4

同被引文献9

  • 1Upadhyaya M, Ruggieri M, Maynard J, et al. Gross deletion of the neurofibromatosis type 1 gene are predominantly with material origin and commonly associated with a learing disability, dysmorphic features and developmental delay[J]. Hum Genet, 1998, 102(5):591-7.
  • 2Shay J, Bacchetti S. A survey of telomerase activity in human cancer[J]. Eur J Cancer, 1997, 33(5). 787-91.
  • 3Palmquist R, Zhang A, Xu D, et al. hTERT gene copy number is not associated with hTERT RNA expression or telomerase activity in colorectal cancer [J].Int J Cancer,2005,116(3):395-400.
  • 4Neumeister P, Albanese C, Balent B, et al. Senescence and epigenetic dysregulation in cancer [J].Int J Biochem Cell Biol, 2002, 34(11):1475-90.
  • 5Atkinson SP, Hoare SF, Glasspool RM, et al. Lack of telomerase gene expression in alternative lengthening of telomere cells is associated with chromatin remodeling of the hTR and hTERT gene promoters[J].Cancer Res,2005,65(17):7585-90.
  • 6Joseph C, Poole, Lucy G, et al. Activity, function, and gene regulation of the catalytic subunit of telomerase (hTERT)[J].Gene, 2001, 269(1-2): 1-12.
  • 7Fujiwara AH, Maesawa C, Honda T, et al. Expression of human telomerase reverse transcriptase splice variants is well correlated with low telomerase activity in osteosarcoma cell lines[J].Int J Oncol,2005,26(4):1009-16.
  • 8Kim NW, Piatyszek MA, Prowse KR, et al. Specific association of human telomerase activity with immortal cells and cancer [J].Science, 1994, 266 (5193): 2011 -5.
  • 9王安训,黄洪章.端粒、端粒酶与口腔颌面部肿瘤[J].中山大学学报(医学科学版),1999,19(S1):97-99. 被引量:2

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