期刊文献+

实时荧光定量PCR检测人脑胶质瘤、髓母细胞瘤中SAMD 14的表达

Expression of SAMD14 in human glioma and medulloblastoma detected by quantitative real time PCR
下载PDF
导出
摘要 目的分析人胶质瘤和髓母细胞瘤中SAMD 14 mRNA的表达情况及其与临床参数间的关系。方法使用实时荧光定量PCR(qRT-PCR)检测10例正常人脑组织、24例胶质瘤患者和11例髓母细胞瘤患者肿瘤组织中SAMD 14 mRNA的相对表达量,分析其表达与患者临床病理学特征的关系。结果胶质瘤、髓母细胞瘤组织中SAMD 14 mRNA的表达水平低于正常脑组织,胶质瘤中SAMD14 mRNA的表达水平高于髓母细胞瘤组织(P<0.05)。SAMD 14 mRNA相对表达量与性别、年龄、肿瘤直径和KPS评分等因素无关(P>0.05)。结论 SAMD 14 mRNA的低表达可能与胶质瘤和髓母细胞瘤的发生、发展有关。 ObjectiveTo analyze the expression of SAMD 14 mRNA in human glioma and medulloblastoma ,and to study their association with clinical features of glioma and medulloblastoma. MethodsThe expression of SAMD 14 mRNA was detected in 10 human normal brain tissues, 24 glioma tissues and 11 medulloblastoma tissues by qRT-PCR, then the relationship of their expression and clinical features were analyzed. ResultsThe expression of SAMD 14 mRNA was lower in glioma and medulloblastoma tissues than in human normal brain tissues. The expression of SMAD14 mRNA was higher in glioma tissues than in medulloblastoma tissues(P<0.05). There is no significant difference between the expression of SMAD14 mRNA and clinical features(Sex, age, tumor diameter and KPS scores,etc). ConclusionThe low expression of SAMD 14 were possibly related to tumorigenesis of glioma and medulloblastoma.
出处 《微创医学》 2017年第2期162-165,186,共5页 Journal of Minimally Invasive Medicine
基金 国家自然科学基金(编号:81460382 81560408) 广西自然科学基金(编号:2014GXNSFAA118231 2014GXNSFAA118089) 广西医科大学青年科学基金(编号:GXMUYSF201409)
关键词 胶质瘤 髓母细胞瘤 SAMD 14 荧光定量PCR Glioma Medulloblastoma SAMD 14 qRT-PCR
  • 相关文献

参考文献1

二级参考文献22

  • 1Iwami K,Natsume A,Wakabayashi T. Cytokine networks in glioma[J]. Neurosurg Rev,2011,34(3):253-263;discussion 263-264.doi:10.1007/s10143-011-0320-y.
  • 2Zhu VF,Yang J,Lebrun DG,et al. Understanding the role ofcytokines in Glioblastoma Multiforme pathogenesis[J]. CancerLett,2012,316(2):139-150. doi:10.1016/j.canlet.2011.11.001.
  • 3Bettelli E,Korn T,Oukka M,et al. Induction and effector functions ofT(H)17 cells[J]. Nature,2008,453(7198):1051-1057. doi:10.1038/nature07036.
  • 4Murugaiyan G,Saha B. Protumor vs antitumor functions of IL-17[J].J Immunol, 2009, 183 (7) : 4169- 4175. doi: 10.4049/jimmunol.0901017.
  • 5Ma W,Wang K,Du J,et al. Multi- dose parecoxib provides animmunoprotective effect by balancing T helper 1(Th1),Th2,Th17and regulatory T cytokines following laparoscopy in patients withcervical cancer[J]. Mol Med Rep,2015,11(4):2999-3008. doi:10.3892/mmr.2014.3003.
  • 6Hu J,Ye H,Zhang D,et al. U87MG glioma cells overexpressing IL-17 acclerate early-stage growth and cause a higher level of CD31mRNA expression in tumor tissues[J]. Oncol Lett,2013,6(4):993-999. doi:10.3892/ol.2013.1518.
  • 7Hu J,Mao Y,Li M,et al. The profile of Th17 subset in glioma[J].Int Immunopharmacol,2011,11(9):1173-1179. doi:10.1016/j.intimp.2011.03.015.
  • 8Maruyama T,Kono K,Mizukami Y,et al. Distribution of Th17 cellsand FoxP3(+)regulatory T cells in tumor-infiltrating lymphocytes,tumor-draining lymph nodes and peripheral blood lymphocytes inpatients with gastric cancer[J]. Cancer Sci,2010,101(9):1947-1954. doi:10.1111/j.1349-7006.2010.01624.x.
  • 9Cardoso CR,Garlet GP,Crippa GE,et al. Evidence of the presenceof T helper type 17 cells in chronic lesions of human periodontaldisease[J]. Oral Microbiol Immunol,2009,24(1):1- 6. doi:10.1111/j.1399-302X.2008.00463.x.
  • 10Gaffen SL. Structure and signalling in the IL-17 receptor family[J]. Nat Rev Immunol,2009,9(8):556- 567. doi:10.1038/nri2586.

共引文献4

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