中国肿瘤临床
中國腫瘤臨床
중국종류림상
CHINESE JOURNAL OF CLINICAL ONCOLOGY
2014年
13期
856-860
,共5页
黄卉%曲育莹%王秋玲%岳贵娟%李娜%李建生
黃卉%麯育瑩%王鞦玲%嶽貴娟%李娜%李建生
황훼%곡육형%왕추령%악귀연%리나%리건생
金龙胶囊%基因芯片%系统生物学%脑肿瘤%机制
金龍膠囊%基因芯片%繫統生物學%腦腫瘤%機製
금룡효낭%기인심편%계통생물학%뇌종류%궤제
Jinlong capsules%gene chip%systems biology%brain tumor%mechanism
目的:利用系统生物学技术分析中药复方金龙胶囊抗脑肿瘤的分子机制。方法:取金龙胶囊组及空白对照组小鼠的原位脑肿瘤组织样本进行基因芯片检测,通过比对获取差异基因;使用一步过连通测算和多步骤隐藏节点测算获得拓扑基因;采用富集分析法分析其生物功能;借助MetaCore平台构建分子机制网络图。结果:与对照组相比,金龙胶囊组共有37个差异基因(倍数>2),106个拓扑基因。金龙胶囊的靶点主要集中在细胞粘附和凋亡、免疫应答、神经组织发育等。结论:金龙胶囊通过诱导神经细胞特有基因表达和抑制干扰素信号转导发挥抗脑肿瘤作用。
目的:利用繫統生物學技術分析中藥複方金龍膠囊抗腦腫瘤的分子機製。方法:取金龍膠囊組及空白對照組小鼠的原位腦腫瘤組織樣本進行基因芯片檢測,通過比對穫取差異基因;使用一步過連通測算和多步驟隱藏節點測算穫得拓撲基因;採用富集分析法分析其生物功能;藉助MetaCore平檯構建分子機製網絡圖。結果:與對照組相比,金龍膠囊組共有37箇差異基因(倍數>2),106箇拓撲基因。金龍膠囊的靶點主要集中在細胞粘附和凋亡、免疫應答、神經組織髮育等。結論:金龍膠囊通過誘導神經細胞特有基因錶達和抑製榦擾素信號轉導髮揮抗腦腫瘤作用。
목적:이용계통생물학기술분석중약복방금룡효낭항뇌종류적분자궤제。방법:취금룡효낭조급공백대조조소서적원위뇌종류조직양본진행기인심편검측,통과비대획취차이기인;사용일보과련통측산화다보취은장절점측산획득탁복기인;채용부집분석법분석기생물공능;차조MetaCore평태구건분자궤제망락도。결과:여대조조상비,금룡효낭조공유37개차이기인(배수>2),106개탁복기인。금룡효낭적파점주요집중재세포점부화조망、면역응답、신경조직발육등。결론:금룡효낭통과유도신경세포특유기인표체화억제간우소신호전도발휘항뇌종류작용。
This article focuses on the research of molecular mechanism of brain tumor treatment using the Jinlong capsule via system biology technology. Methods:Human Genome U133 Plus 2.0 gene chip was used to detect the genes of samples, in-cluding the brain tumor tissues of nude mice after Jinlong capsule intervention and those of blank control group mice. Differentially ex-pressed genes were identified based on fold change between the two groups. To identify the upstream regulators of the response signa-tures, the differentially expressed genes were subjected to interactome analysis by one-step overconnectivity test and multi-step hidden node algorithm. A set of genes preferentially connected to differentially expressed genes via direct interactions and pathways (called to-pologically significant genes) was generated. Concurrent pathway enrichment analysis on key pathways, processes, and functional units of both differentially expressed genes and topologically significant genes was performed to identify the most likely signaling pathways connecting regulators and effector genes. Finally, condition-specific networks (called causal network) were built to model molecular events by using a set of manually annotated protein interactions, pathways, and proteins and a toolkit of algorithms and filters on Meta-Core platform. Results:A total of 37 differentially expressed genes have been identified between Jinlong capsule-treated sample and ve-hicle sample with fold change of 2. Connection analysis identified 106 topologically significant genes. The main feature of the causal network is stimulation of neural cell specific genes that regulate normal cell physiology, particularly developmental processes and apop-tosis. Another important effect of the Jinlong capsule is its inhibition of the gene markers of interferon response, suggesting signaling in-hibition, followed by de-activation of immune response. Conclusion:Jinlong capsule exerts an anti-neoplastic effect by inducing stimu-lation of neural cell and by inhibiting interferon signal transduction.