期刊文献+

泌乳素腺瘤基因表达谱的建立与分析 被引量:1

Establishment and analysis of gene-expression profiles in prolactinomas
下载PDF
导出
摘要 目的建立和分析泌乳素腺瘤的基因表达谱。方法应用人全基因组寡核苷酸芯片HG-U133A2.0检测2例泌乳素腺瘤组织和2例混合的正常垂体组织的基因表达谱,对差异表达基因进行筛选和生物信息学分析。结果成功建立正常垂体与泌乳素腺瘤的基因表达谱,筛选出与泌乳素腺瘤相关的上调基因313条,下调基因856条。这些差异基因功能聚类显示主要涉及分子结合、凋亡或肿瘤相关、代谢、信号传导、细胞周期等多个分子通路。结论基因表达谱的建立有助于分析、研究泌乳素腺瘤的分子机制。 Objective To establish and analyze the gene-expression profiles in the prolactinomas.Methods The gene expression profiles in 2 prolactinoma samples and 2 normal pooled pituitary tissues samples were determined by the whole genome oligonucleotide microarray(Affymetrix 133 plus 2.0).Differentially expressed genes were screened out and their bioinformatics was analyzed.Results The gene expression profiles in the normal pooled pituitary tissues and prolactinomas were successful established.There were 313 up-regulated genes and 856 down-regulated genes in the prolactinomas compared to the normal pooled pituitary tissues.These differentially expressed genes mainly involved in the molecular pathways of molecular binding,apoptosis or tumor,metabolism,signal transduction activity and cell-cycle.Conclusions The establishment of gene expression profiles in the prolactinoma is helpful to analysis the molecular mechanism of pathogenesis of the prolactinoma.
出处 《中国临床神经外科杂志》 2010年第7期400-403,共4页 Chinese Journal of Clinical Neurosurgery
关键词 泌乳素腺瘤 寡核苷酸芯片 基因表达谱 Prolactinoma Oligonucleotide microarray Gene expression profile
  • 相关文献

参考文献7

  • 1Heaney AP,Melmed S.Molecular targets in pituitary tumours[J].Nat Rev Cancer,2004,4(4):285-295.
  • 2Melmed S.Mechanisms for pituitary tumorigenesis:the plastic pituitary[J].J Clin Invest,2003,112(11):1603-1618.
  • 3Qian X,Scheithauer BW,Kovacs K,et al.DNA microarrays:recent developments and applications to the study of pituitary tissues[J].Endocrine,2005,28(1):49-56.
  • 4干小强,卢亦成,丁学华.生物芯片在垂体腺瘤分子机制研究中的应用[J].中国微侵袭神经外科杂志,2007,12(2):91-93. 被引量:5
  • 5Abdullah-Sayani A,Bueno-de-Mesquita JM,van de Vijver MJ.Technology insight:tuning into the genetic orchestra using microarrays--limitations of DNA microarrays in clinical practice[J].Nat Clin Pract Oncol,2006,3(9):501-516.
  • 6Jagannathan J,Dumont AS,Prevedello DM,et al.Genetics of pituitary adenomas:current theories and future implications[J].Neurosurg Focus,2005,19(5):E4.
  • 7Levy A,Lightman S.Molecular defects in the pathogenesis of pituitary tumours[J].Front Neuroendocrinol,2003,24(2):94-127.

二级参考文献15

  • 1HEANEY A P, MELMED S. Molecular targets in pituitary tumors [J]. Nat Rev Cancer, 2004, 4(4): 285-295.
  • 2MELMED S. Mechanisms for pituitary tumorigenesis: the plastic pituitary [J]. J Clin Invest, 2003, 112(11): 1603-1618.
  • 3STEARS R L, MARTINSKY T, SCHENA M. Trends in microarray analysis [J]. Nat Med, 2003, 9(1): 140-145.
  • 4ASA S L, EZZAT S, The pathogenesis of pituitary tumours[J]. Nat Rev Cancer, 2002, 2(11): 836-849.
  • 5Al-SHRAIM M, AL-GAHTANY M, AL-OTAIBI M, et al.Molecular biology of pituitary tumors [J]. Endocrinology,2004, 14: 359-367.
  • 6MOHAMMAD H P, SEACHRIST D D, QUIRK C C, et al.Reexpression of p8 contributes to tumorigenic properties of pituitary cells and appears in a subset of prolactinomas in transgenic mice that hypersecrete luteinizing hormone [J].Mol Endocrinol, 2004, 18(10): 2583-2593.
  • 7FURUMOTO H, YING H, CHANDRAMOULI G V, et al.An unliganded thyroid hormone beta receptor activates the cyclin D1/cyclin-dependent kinase/retinoblastoma/E2F pathway and induces pituitary tumorigenesis [J]. Mol Cell Biol,2005, 25(1): 124-135.
  • 8ZHAN X, EVANS C O, OYESIKU N M, et al. Proteomics and transcriptomics analyses of secretagogin down-regulation in human non-functional pituitary adenomas [J]. Pituitary, 2003, 6(4): 189-202.
  • 9WOOD W M, SARAPURA V D, DOWDING J M, et al.Early gene expression changes preceding thyroid hormone-induced involution of a thyrotrope tumor [J]. Endocrinology,2002, 143(2): 347-359.
  • 10EVANS C O, YOUNG A N, BROWN M R, et al. Novel patterns of gene expression in pituitary adenomas identified by complementary deoxyribonucleic acid microarrays and quantitative reverse transcription-polymerase chain reaction[J]. J Clin Endocrinol Metab, 2001, 86(7): 3097-3107.

共引文献4

同被引文献5

引证文献1

二级引证文献2

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