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FRAT1和β-catenin在人类脑胶质瘤中的表达及其意义 被引量:3

Expression of FRAT1 and β-catenin in human brain glioma and their significances
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摘要 目的 探讨FRAT1、β-catenin蛋白在人类脑胶质瘤中的表达情况及两者关系,研究二者与临床病理分级的关系.方法 应用免疫组织化学方法检测FRAT1及β-catenin蛋白在84例人类脑胶质瘤组织和6例人正常脑组织中的表达水平.结果 人类脑胶质瘤组织中FRAT1与β-catenin蛋白表达阳性率分别为66.7%(56/84)和77.4%(65/84),人正常脑组织均未见FRAT1与β-catenin蛋白表达.在Ⅰ、Ⅱ、Ⅲ、Ⅳ级脑胶质瘤标本中,FRAT1免疫反应评分分别为1.25±1.77、2.64±3.13、4.63±3.17和6.52±3.42,与人正常脑组织相比,差异有统计学意义(P<0.01),β-catenin分别为1.06±1.18、2.86±2.75、4.74±3.07和7.15±1.90,与人正常脑组织相比,差异有统计学意义(P<0.01).FRAT1与β-catenin表达水平随着脑胶质瘤病理级别的增高而升高(r=0.55,P< 0.01;r=0.70,P<O.01),且FRAT1与β-catenin表达水平呈正相关(r=0.77,P< 0.01).结论 FRAT1与β-catenin高表达可能与人类脑胶质瘤的发生、发展密切相关.为Wnt/β-catenin信号通路的研究开辟了新的领域,也为脑胶质瘤病理诊断和基因治疗提供了新的靶点. Objective To investigate the expression of FRAT1 and β-catenin in human brain glioma,analyze the correlation between the expression and clinical pathological grades and the correlation of the two genes.Methods FRAT1 and β-catenin were detected by immunohistochemistry in 84 human brain glioma tissues and 6 human normal brain tissues.Results 66.7 % (56/84) and 77.4 % (65/84) of human brain glioma tissues expressed FRAT1 and β-catenin protein,whereas no FRAT1 and β-catenin protein expression was detected in human normal brain tissues.The expression levels of FRAT1 and ββ-catenin increased markedly with the ascending of pathologic grade of tumor specimens (r =0.55,P 〈 0.01,r =0.70,P 〈 0.01),there was a positive correlation between FRAT1 and β-catenin (r =0.77,P 〈 0.01).Conclusion FRAT1 and β-catenin over-expression maybe closely related with occurrence and development of human brain gliomas.The results provide important supplements for the research of Wnt/β-catenin pathway.Meanwhile,FRAT1 may act as a valuable biomarker for molecular diagnosis of glioma and a potential target for gene therapy of glioma.
出处 《肿瘤研究与临床》 CAS 2013年第5期309-311,315,共4页 Cancer Research and Clinic
基金 基金项目:国家自然科学基金青年基金(81201991) 山西省基础研究计划青年科技研究基金(2012021035-5) 山西医科大学青年基金(02201116) 山西医科大学第一医院博士启动基金(YB1111)
关键词 神经胶质瘤 免疫组织化学 FRAT1 Β-CATENIN WNT Β-CATENIN信号通路 Glioma Immunohistochemistry FRAT1 β-catenin Wnt/β-catenin pathway
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参考文献12

  • 1Hess KR, Broglio KR, Bondy ML. Adult glioma incidence trends inthe United States, 1977-2000. Cancer, 2004, 101: 2293-2299.
  • 2Saitoh T, Mine T, Katoh M. Molecular cloning and expression of proto-oncogene FRAT1 in human cancer. Int J Oncol, 2002,20: 785-789.
  • 3Wang Y, Hewitt SM, Liu S, et al. Tissue microarray analysis of humanFRAT1 expression and its correlation with the subcellular localisationof beta-catenin in ovarian tumours. Br J Cancer, 2006, 94: 686-691.
  • 4Wang Y, Liu S, Zhu H, et al. FRAT1 overexpression leads to aberrantactivation of beta-catenin/TCF pathway in esophageal squamous cellcarcinoma. Int J Cancer, 2008, 123: 561-568.
  • 5Jonkers J, Weening JJ, van der Valk M, et al. Overexpression of Fratlin transgenic mice leads to glomerulosclerosis and nephroticsyndrome, and provides direct evidence for the involvement of Fratl inlymphoma progression. Oncogene, 1999, 18: 5982-5990.
  • 6Saitoh T, Katoh M. FRAT1 and FRAT2, clustered in humanchromosome 10q24.1 region, are up-regulated in gastric cancer. Int JOncol, 2001, 19:311-315.
  • 7Zhang Y, Yu JH, Lin XY, et al. Overexpression of Fratl correlateswith malignant phenotype and advanced stage in human non-small celllung cancer. Virchows Arch, 2011, 459: 255-263.
  • 8Louis DN, Ohgaki H, Wiestler OD, et al. The 2007 WHOclassification of tumours of the central nervous system. ActaNeuropathol, 2007, 114: 97-109.
  • 9Remmele W, Hildebrand U, Hienz H A, et al. Comparativehistological, histochemical, immunohistochemical and biochemicalstudies on oestrogen receptors, lectin receptors, and Barr bodies inhuman breast cancer. Virchows Arch A Pathol Anat Histopathol,1986, 409: 127-147.
  • 10van der Flier LG, Sabates-Bellver J, Oving I, et al. The IntestinalWnt/TCF Signature. Gastroenterology, 2007,132: 628-632.

同被引文献32

  • 1Charles DS,David HR. Glioma stem cells:a midterm exam[J].{H}CELL,2008.832-847.
  • 2Singh SK,Clarke !D,Terasaki M. Identification ofa cancer stem cell in human brain tumors[J].{H}CANCER RESEARCH,2003.5821-5828.
  • 3Nakagawa M,Koyanagi M,Tanabe K. Generation of induced pluripotent stem cells without Myc from mouse and human fibroblasts[J].{H}Nature Biotechnology,2008.101-106.
  • 4Baboo RM,Maher EA,Ligon KL. Epidermal growth factor receptor and lnk4a/aft:convergent mechanisms governing terminal differentiation and transformation along the neural stem cell to astrocyte axis[J].{H}CANCER CELLS,2002.269-277.
  • 5Li J,Yen C,Liaw D. PTEN,a putative protein tyrosine phosphatase gene mutated in human brain,breast and prostate cancer[J].{H}SCIENCE,1997.1943-1947.
  • 6Chow LM,Baker SJ. PTEN function in normal and neoplastic growth[J].{H}CANCER LETTERS,2006.184-196.
  • 7Fan X,Aalto Y,Sanko SG. Genetic profile,PTEN mutation and therapatic role of PTEN in glioblastomas[J].{H}International Journal of Oncology,2002.1141-1150.
  • 8Yang L,Xie G,Fan Q. Activation ofthe hedgehog-signaling pathway in human cancer and the clinical implications[J].{H}ONCOGENE,2010.469-481.
  • 9Beauchamp E,Bulut G,Abaan O. GLI1 is a direct transcriptional target of EWS-FLI1 oncoprotein[J].{H}Journal of Biological Chemistry,2009.9074-9082.
  • 10Mercher T,Cornejo MG,Sears C. Notch signaling specifies megakaryocyte development from hematopoietic stem cells[J].Cell Stem Cell,2008.314-326.

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