期刊文献+

miR-497的生物信息学分析及其在肺腺癌中表达的验证 被引量:1

Bioinformatics analysis of miR- 497 and its expression in lung adenocarcinoma
下载PDF
导出
摘要 目的:对hsa-miR-497进行靶基因和功能生物信息学分析预测,为后续深入研究其生物学功能和调控机制提供实验理论指导,并对其在肺腺癌中的表达进行初步验证。方法:利用PubMed检索miR-497相关文章,通过miRBase在线工具分析miR-497碱基序列、染色体定位等信息。应用Targetscan及miRDB两种预测工具对miR-497进行靶基因预测取其交集,应用R中clusterProfiler包进行靶基因功能富集及信号转导通路富集分析。最后应用RT-PCR定量检测miR-497在新鲜肺腺癌及癌旁组织中的表达。结果:miR-497在多物种间具有高度的保守性,功能富集分析预测的结果显示miR-497调控的靶基因集合功能主要富集于输尿管芽生长、穿膜受体蛋白激酶、肽结合、分支形态发生和膜筏等过程(P<0.05)。KEGG生物通路显著富集于调控干细胞多能性、癌、Wnt及Rap1信号通路等(P<0.001)。miR-497在肺腺癌组织中表达明显低于癌旁组织,差异有统计学意义(P<0.05)。结论:miR-497通过靶基因调控多个生物学过程及疾病通路,尤其在肿瘤方向的生物学功能值得进一步研究,miR-497在肺腺癌中低表达为研究肺腺癌的发生及发展及治疗提供了新的方向。 Objective:To predict the target genes and functional bioinformatics analysis of miR-497,and provide theoretical guidance for further research on the biological function and regulatory mechanism of miR-497.Furthermore,its expression in lung adenocarcinoma was verified.Methods:Using PubMed to retrieve the relevant articles of miR-497,analyze its base sequence,chromosome location and other information through miRBase online tool,and analyze its conservative nature.Then,targetscan and miRDB were applied to predict the intersection of the target gene of miR-497.Finally,the target gene function enrichment and signal transduction pathway enrichment analysis were performed by using the confirmed target gene,the expression of miR-497 in fresh lung cancer and adjacent tissues was quantitatively detected by RT-PCR.Results:The results showed that the miR-497 was highly conservative among multiple species. The target gene function of has-miR-497 was mainly focused on ureteric bud development,transmembrane receprot protein kinase,peptide binding,morphogenesis of a branching and membrane raft(P<0.05).KEGG biological pathway was mainly concentrated on the interaction pathway of regulation of stem cell pluripotent,pathways in cancer,Wnt and Rap1 signaling pathway(P<0.001).The expression of miR-497 in lung cancer tissues was significantly lower than that in adjacent tissues(P<0.05).Conclusion:miR-497 regulates multiple biological processes and disease pathways through target gene,especially in the direction of tumor.Lower expression of miR-497 in lung adenocarcinoma provides a new direction for predicting the occurrence,development and treatment of lung cancer.
作者 胡文铧 范欢 陈婷 王永存 刘曙光 HU Wenhua;FAN Huan;CHEN Ting;WANG Yongcun;LIU Shuguang(Department of Pathology,Affiliated Hospital of Guangdong Medical University,Guangdong Zhanjiang 524000,China;Department of Pathology,the Eighth Affiliated Hospital,Sun Yat-sen University,Guangdong Shenzhen 518000,China;Clinical Research Center,Affiliated Hospital of Guangdong Medical University,Guangdong Zhanjiang 524000,China;Department of Oncology,Affiliated Hospital of Guangdong Medical University,Guangdong Zhanjiang 524000,China)
出处 《现代肿瘤医学》 CAS 北大核心 2021年第5期801-806,共6页 Journal of Modern Oncology
基金 深圳市福田区卫生公益性科研项目(编号:FTWS2018043,FTWS2018047)。
关键词 miR-497-5p 靶基因 基因功能注释 信号通路 生物信息学 肺腺癌 miR-497 target genes gene function annotation signaling pathway bioinformatics lung adenocarcino-ma
  • 相关文献

参考文献2

二级参考文献34

  • 1Xiang X. miRNA-584-Sp exerts tumor suppressive functions in human neuroblastoma through repressing transcription of matrix metalloproteinase 14. Biochimica et Biophysica aeta, 2015,6:1743.
  • 2Huang J, Ni S, Li D, et al. An insertion/deletion polymor- phism at miRNA-122 binding site in the ILIA is associated with a reduced risk of cervical squamous cell carcinoma. Genetic Testing and Molecular Biomarkers,2015,19:331.
  • 3Kouri F, Ritner C, Stegh H. miRNA-182 and the regulati- on of the glioblastoma phenotype-toward miRNA-based precision therapeutics. Cell Cycle, 2015,10:1538.
  • 4BarteI P. MicroRNAs: target recognition and regulatory fun- ctions. Cell, 2009,1:215.
  • 5Enright J. Micro RNA targets in Drosophila. Genome biology, 2003,1:1186.
  • 6Kiriakidou M. A combined computational-experimental ap- proach predicts human micro RNA targets.Genes & Develop- ment,2004,18:1165.
  • 7Rehmsmeier M, Steffen P, Hochsmann M, et al. Fast and ef fective prediction of micro RNA/target duplexes. Rna, 2004, 10:1507.
  • 8Lewis P, Shih H, Jones-Rhoades W, et al. Prediction of mammalian microRNA targets. Cell, 2003,115:787.
  • 9Lewis P, Burge B, Bartet P. Conserved seed pairing, often flanked by adenosines, indicates that thousands of human genes are microRNA targets. Cell, 2005,120:15.
  • 10Rusinov V, Baev V, Minkov N, et al. MicroInspector: a web tool for detection of miRNA binding sites in an RNA seque- nce. Nucleic Acids Research,2005,33:696.

共引文献10

同被引文献8

引证文献1

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