中国肿瘤临床
中國腫瘤臨床
중국종류림상
CHINESE JOURNAL OF CLINICAL ONCOLOGY
2014年
16期
1021-1025
,共5页
王红艳%郑少秋%涂永生%张雅洁
王紅豔%鄭少鞦%塗永生%張雅潔
왕홍염%정소추%도영생%장아길
miR-29b%肺癌%靶基因%生物信息学
miR-29b%肺癌%靶基因%生物信息學
miR-29b%폐암%파기인%생물신식학
miR-29b%lung cancer%target gene%bioinformatics
目的:应用生物信息学分析A549细胞中在CD133阳性低表达的miR-29b的靶基因及其功能,为以miR-29b为靶点的肿瘤研究提供线索。方法:利用miRNA PCR芯片筛选A549细胞中CD133阳性和CD133阴性差异表达的miRNA,选用miRecords预测miR-29b的靶基因,合并已证实的靶基因,利用GOEAST和DAVID数据库对所得靶基因进行功能富集分析和信号转导通路富集分析。结果:A549细胞中与CD133阴性比较,miR-29b在CD133阳性中表达下调。miR-29b靶基因有106个,其靶基因功能富集于结合和细胞外基质形成等作用(P<0.01);信号转导通路显著富集于JAK-STAT和TGF-β等信号转导通路(P<0.05)。结论:miR-29b可能与肺癌转移相关,miR-29b的靶基因显著富集在与肿瘤相关的信号通路中。
目的:應用生物信息學分析A549細胞中在CD133暘性低錶達的miR-29b的靶基因及其功能,為以miR-29b為靶點的腫瘤研究提供線索。方法:利用miRNA PCR芯片篩選A549細胞中CD133暘性和CD133陰性差異錶達的miRNA,選用miRecords預測miR-29b的靶基因,閤併已證實的靶基因,利用GOEAST和DAVID數據庫對所得靶基因進行功能富集分析和信號轉導通路富集分析。結果:A549細胞中與CD133陰性比較,miR-29b在CD133暘性中錶達下調。miR-29b靶基因有106箇,其靶基因功能富集于結閤和細胞外基質形成等作用(P<0.01);信號轉導通路顯著富集于JAK-STAT和TGF-β等信號轉導通路(P<0.05)。結論:miR-29b可能與肺癌轉移相關,miR-29b的靶基因顯著富集在與腫瘤相關的信號通路中。
목적:응용생물신식학분석A549세포중재CD133양성저표체적miR-29b적파기인급기공능,위이miR-29b위파점적종류연구제공선색。방법:이용miRNA PCR심편사선A549세포중CD133양성화CD133음성차이표체적miRNA,선용miRecords예측miR-29b적파기인,합병이증실적파기인,이용GOEAST화DAVID수거고대소득파기인진행공능부집분석화신호전도통로부집분석。결과:A549세포중여CD133음성비교,miR-29b재CD133양성중표체하조。miR-29b파기인유106개,기파기인공능부집우결합화세포외기질형성등작용(P<0.01);신호전도통로현저부집우JAK-STAT화TGF-β등신호전도통로(P<0.05)。결론:miR-29b가능여폐암전이상관,miR-29b적파기인현저부집재여종류상관적신호통로중。
Objective:This paper aims to bioinformatically analyze the target genes of miR-29b and to provide clues for cancer research targeting miR-29b. Methods:The differential expression levels of miRNAs in CD133+and CD133-A549 cells were detected using the miRNA PCR chip. Real-time polymerase chain reaction was performed to verify the partially differential expression of miR-NAs. Target genes of miR-29b were predicted by miRecords and analyzed by gene ontology and signal transduction pathway enrich-ment analysis. Results: The miR-29b expression was significantly decreased in the CD133+A549 cells compared with that in the CD133-cells. The number of miR-29b target genes was 106. The functions of these target genes were enriched in binding and extracel-lular matrix structural constituent (P<0.01). The JAK-STAT and TGF-βsignal transduction pathways were significantly enriched (P<0.05). Conclusion:The abnormal expression of miR-29b may be related to metastasis. Some of the predicted target genes of miR-29b were significantly enriched in the signaling pathways in relation to the tumors.