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信号通路和 miRNA 调控通路中非甾体抗炎药作用的建模。

Modeling of non-steroidal anti-inflammatory drug effect within signaling pathways and miRNA-regulation pathways.

机构信息

Institute for Medical Informatics, Biometry and Epidemiology, Ludwig-Maximilians-University Munich, Munich, Germany.

出版信息

PLoS One. 2013 Aug 14;8(8):e72477. doi: 10.1371/journal.pone.0072477. eCollection 2013.

Abstract

To date, it is widely recognized that Non-Steroidal Anti-Inflammatory Drugs (NSAIDs) can exert considerable anti-tumor effects regarding many types of cancers. The prolonged use of NSAIDs is highly associated with diverse side effects. Therefore, tailoring down the NSAID application onto individual patients has become a necessary and relevant step towards personalized medicine. This study conducts the systemsbiological approach to construct a molecular model (NSAID model) containing a cyclooxygenase (COX)-pathway and its related signaling pathways. Four cancer hallmarks are integrated into the model to reflect different developmental aspects of tumorigenesis. In addition, a Flux-Comparative-Analysis (FCA) based on Petri net is developed to transfer the dynamic properties (including drug responsiveness) of individual cellular system into the model. The gene expression profiles of different tumor-types with available drug-response information are applied to validate the predictive ability of the NSAID model. Moreover, two therapeutic developmental strategies, synthetic lethality and microRNA (miRNA) biomarker discovery, are investigated based on the COX-pathway. In conclusion, the result of this study demonstrates that the NSAID model involving gene expression, gene regulation, signal transduction, protein interaction and other cellular processes, is able to predict the individual cellular responses for different therapeutic interventions (such as NS-398 and COX-2 specific siRNA inhibition). This strongly indicates that this type of model is able to reflect the physiological, developmental and pathological processes of an individual. The approach of miRNA biomarker discovery is demonstrated for identifying miRNAs with oncogenic and tumor suppressive functions for individual cell lines of breast-, colon- and lung-tumor. The achieved results are in line with different independent studies that investigated miRNA biomarker related to diagnostics of cancer treatments, therefore it might shed light on the development of biomarker discovery at individual level. Particular results of this study might contribute to step further towards personalized medicine with the systemsbiological approach.

摘要

迄今为止,人们普遍认为非甾体抗炎药(NSAIDs)对多种癌症具有显著的抗肿瘤作用。然而,长期使用 NSAIDs 会引起多种副作用。因此,针对个体患者定制 NSAID 的应用已成为迈向个性化医学的必要和相关步骤。本研究采用系统生物学方法构建了一个包含环氧化酶(COX)途径及其相关信号通路的分子模型(NSAID 模型)。该模型整合了四个肿瘤标志性特征,以反映肿瘤发生的不同发展方面。此外,还开发了基于 Petri 网的通量比较分析(FCA),将个体细胞系统的动态特性(包括药物反应性)转化到模型中。该模型应用了具有可用药物反应信息的不同肿瘤类型的基因表达谱来验证 NSAID 模型的预测能力。此外,还基于 COX 途径研究了两种治疗开发策略,即合成致死和 microRNA(miRNA)生物标志物发现。总之,本研究结果表明,该 NSAID 模型涉及基因表达、基因调控、信号转导、蛋白质相互作用和其他细胞过程,能够预测不同治疗干预(如 NS-398 和 COX-2 特异性 siRNA 抑制)下个体细胞的反应。这强烈表明该模型能够反映个体的生理、发育和病理过程。miRNA 生物标志物发现的方法用于鉴定具有致癌和肿瘤抑制功能的 miRNA,针对乳腺癌、结肠癌和肺癌细胞系的个体。所获得的结果与研究癌症治疗相关 miRNA 生物标志物的不同独立研究一致,因此,它可能为个体水平的生物标志物发现的发展提供启示。本研究的特定结果可能有助于进一步推进基于系统生物学的个性化医学。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ec2/3743815/c7d820dfdbfb/pone.0072477.g001.jpg

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