期刊文献+

用文献轮廓挖掘鼻咽癌微阵列表达数据 被引量:2

Mining gene expression microarray data of nasopharyngeal carcinoma by literature profiling
下载PDF
导出
摘要 目的 探索鼻咽癌异常信号通路。方法 根据鼻咽癌微阵列表达谱,采用基于文献轮廓的数据挖掘方法,从Medline文献数据库中提取与基因相关的文献并分析词的频率,再根据重复发生和共发生的过滤标准提取功能相关的词,最后根据词的发生频率对基因进行功能聚类。结果 基因表达谱的112个差异表达基因聚成16组功能类别:4组暗示EBV感染、6组显示鼻咽癌变过程、2组参与能量代谢、1组提示蛋白的异常磷酸化、2组与其它疾病相关、1组与肌肉组织活性相关。肿瘤发生发展过程中常见的P53和Rb信号通路的异常在本研究中则未发现。结论 鼻咽癌的发生发展可能由特殊的信号通路引起。 Objective To study abnormal signal pathway in nasopharyngeal carcinoma (NPC). Method NPC gene expression microarray data was mined by analysis of literature profiles generated by extracting the frequencies of certain terms from the abstracts stored in the Medline literature database. The terms were then filtered on the basis of both repetitive occurrence and co-occurrence among multiple gene entries. Finally, clustering analysis was performed on the retained frequency values, shaping a coherent picture of the functional relationship among large and heterogeneous lists of genes. Result Sixteen function groups were found among 112 abnormally expressed genes, including 4 groups indicative of Epstein-Barr virus (EBV) infection, 6 groups indicative of normal nasopharyngeal tissues that acquired essential capabilities to develop into tumor, 2 groups involved in energy metabolism, 1 group suggesting abnormal phosphorylation of proteins, 2 groups related tother diseases, and 1 group associated with muscle activities. The pathways of p53 and Rb, which were frequently abnormal during tumor progression, were not found in these groups. Conclusion Initiation and progression of NPC may be caused by special signal transduction pathways.
出处 《第一军医大学学报》 CSCD 北大核心 2004年第7期798-801,共4页 Journal of First Military Medical University
基金 广东省"十五"专项基金(A1080201)~~
关键词 鼻咽癌 信号通路 微阵列 数据挖掘 生物信息学 nasopharyngeal carcinoma signal microarray data-mining bioinformation
  • 相关文献

参考文献3

二级参考文献19

  • 1Chaussabel D, Sher A. Mining microarray expression data by literature profiling[J]. Genome Biol, 2002, 3(10): 1-16.
  • 2Chen Y, Dougherty ER, Bittner ML. Ratio-based decisions and the quantitative analysis of cDNA microarray images[J]. J Biomed Optics, 1997, 2(4): 364-74.
  • 3Habets GG, van der Kammen RA, Stare JC, et al. Sequence of the human invasion-inducing TIAMI gene, its conservation in evolution and its expression in tumor cell lines of different tissue origins [J].Oncogene, 1995, 10(7): 1371-6.
  • 4Lambert JM, Lambert QT, Reuther GW, et al. Tiaml mediates Ras activation of Rac by a PI(3)K-independent mechanism [J ]. Nat Cell Biol, 2002, 4(8): 621-5.
  • 5Malliri A, van der Kammen RA, Clark K, et al. Mice deficient in the Rac activator Tiaml are resistant to Ras-induced skin tumours [ J].Nature, 2002, 417(6891): 867-71.
  • 6Sun XF, Ekberg H, Zhang H, et al. Overexpression ofras is an independent prognostic factor in colorectal adenocarcinoma [ J ]. APMIS,1998, 106(6): 657-64.
  • 7Otsuki Y, Tanaka M, Yoshii S, et al. Tumor metastasis suppressor nm23Hl regulates Racl GTPase by interaction with Tiaml [J]. Proc Natl Acad Sci USA, 2001,98(8): 4385-90.
  • 8Amendola R, Martinez R, Negroni A, et al. DR-nm23 expression affects neuroblastoma cell differentiation, integrin expression, and adhesion characteristics [J ]. Med Pediatr Oncol, 2001, 36(1 ): 93-6.
  • 9Bourguignon LY, Zhu H, Shao L, et al. Ankyrin-Tiaml interaction promotes Racl signaling and metastatic breast tumor cell invasion and migration[J]. J Cell Biol, 2000, 150(1): 177-91.
  • 10Martinez R, Venturelli D, Perrotti D, et al. Gene structure, promoter activity, and chromosomal location of the DR-nm23 gene, a related member of the nm23 gene family[J ]. Cancer Res, 1997, 57(6): 1180-7.

共引文献19

同被引文献63

引证文献2

二级引证文献10

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