基于多尺度agent的框架与基于约束的癌症代谢网络模型相结合,用于模拟无血管肿瘤生长

IF 3.743 Q2 Biochemistry, Genetics and Molecular Biology Molecular BioSystems Pub Date : 2017-07-24 DOI:10.1039/C7MB00050B
Mehrdad Ghadiri, Mahshid Heidari, Sayed-Amir Marashi and Seyed Hasan Mousavi
{"title":"基于多尺度agent的框架与基于约束的癌症代谢网络模型相结合,用于模拟无血管肿瘤生长","authors":"Mehrdad Ghadiri, Mahshid Heidari, Sayed-Amir Marashi and Seyed Hasan Mousavi","doi":"10.1039/C7MB00050B","DOIUrl":null,"url":null,"abstract":"<p >In recent years, many efforts have been made in the field of computational modeling of cancerous tumors, in order to obtain a better understanding and predictions of their growth patterns. Furthermore, constraint-based modeling of metabolic networks has become increasingly popular, which is appropriate for the systems-level reconstruction of cell physiology. The goal of the current study is to integrate a multiscale agent-based modeling framework with a constraint-based metabolic network model of cancer cells in order to simulate the three dimensional early growth of avascular tumors. In order to develop the integrated model, a previously published generic metabolic network model of cancer cells was introduced into a multiscale agent-based framework. This model is initiated with a single tumor cell. Nutrients can diffuse through the simulation space and the cells uptake or excrete metabolites, grow, proliferate or become necrotic based on certain defined criteria and flux values of particular reactions. The simulation was run for a period of 20 days and the plots corresponding to various features such as the growth profile and necrotic core evolution were obtained. These features were compared with the ones observed in other (experimental) studies. One interesting characteristic of our modeling is that it provides us with the ability to predict gene expression patterns through different layers of a tumor, which can have important implications, especially in drug target selection in the field of cancer therapy.</p>","PeriodicalId":90,"journal":{"name":"Molecular BioSystems","volume":null,"pages":null},"PeriodicalIF":3.7430,"publicationDate":"2017-07-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1039/C7MB00050B","citationCount":"13","resultStr":"{\"title\":\"A multiscale agent-based framework integrated with a constraint-based metabolic network model of cancer for simulating avascular tumor growth†\",\"authors\":\"Mehrdad Ghadiri, Mahshid Heidari, Sayed-Amir Marashi and Seyed Hasan Mousavi\",\"doi\":\"10.1039/C7MB00050B\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >In recent years, many efforts have been made in the field of computational modeling of cancerous tumors, in order to obtain a better understanding and predictions of their growth patterns. Furthermore, constraint-based modeling of metabolic networks has become increasingly popular, which is appropriate for the systems-level reconstruction of cell physiology. The goal of the current study is to integrate a multiscale agent-based modeling framework with a constraint-based metabolic network model of cancer cells in order to simulate the three dimensional early growth of avascular tumors. In order to develop the integrated model, a previously published generic metabolic network model of cancer cells was introduced into a multiscale agent-based framework. This model is initiated with a single tumor cell. Nutrients can diffuse through the simulation space and the cells uptake or excrete metabolites, grow, proliferate or become necrotic based on certain defined criteria and flux values of particular reactions. The simulation was run for a period of 20 days and the plots corresponding to various features such as the growth profile and necrotic core evolution were obtained. These features were compared with the ones observed in other (experimental) studies. One interesting characteristic of our modeling is that it provides us with the ability to predict gene expression patterns through different layers of a tumor, which can have important implications, especially in drug target selection in the field of cancer therapy.</p>\",\"PeriodicalId\":90,\"journal\":{\"name\":\"Molecular BioSystems\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":3.7430,\"publicationDate\":\"2017-07-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1039/C7MB00050B\",\"citationCount\":\"13\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Molecular BioSystems\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2017/mb/c7mb00050b\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"Biochemistry, Genetics and Molecular Biology\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular BioSystems","FirstCategoryId":"1085","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2017/mb/c7mb00050b","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 13

摘要

近年来,为了更好地理解和预测癌性肿瘤的生长模式,在癌性肿瘤的计算建模领域做出了许多努力。此外,基于约束的代谢网络建模越来越受欢迎,这适用于细胞生理学的系统级重建。本研究的目标是将基于多尺度agent的建模框架与基于约束的癌细胞代谢网络模型相结合,以模拟无血管肿瘤的三维早期生长。为了开发集成模型,将先前发表的癌细胞通用代谢网络模型引入到基于多尺度agent的框架中。该模型以单个肿瘤细胞为起始点。营养物质可以通过模拟空间扩散,细胞摄取或排泄代谢物,根据特定反应的特定标准和通量值生长、增殖或坏死。模拟运行了20天,得到了与生长剖面和坏死核演化等各种特征相对应的图。这些特征与其他(实验性)研究中观察到的特征进行了比较。我们的模型的一个有趣的特点是,它为我们提供了通过肿瘤的不同层预测基因表达模式的能力,这可能具有重要的意义,特别是在癌症治疗领域的药物靶点选择方面。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
A multiscale agent-based framework integrated with a constraint-based metabolic network model of cancer for simulating avascular tumor growth†

In recent years, many efforts have been made in the field of computational modeling of cancerous tumors, in order to obtain a better understanding and predictions of their growth patterns. Furthermore, constraint-based modeling of metabolic networks has become increasingly popular, which is appropriate for the systems-level reconstruction of cell physiology. The goal of the current study is to integrate a multiscale agent-based modeling framework with a constraint-based metabolic network model of cancer cells in order to simulate the three dimensional early growth of avascular tumors. In order to develop the integrated model, a previously published generic metabolic network model of cancer cells was introduced into a multiscale agent-based framework. This model is initiated with a single tumor cell. Nutrients can diffuse through the simulation space and the cells uptake or excrete metabolites, grow, proliferate or become necrotic based on certain defined criteria and flux values of particular reactions. The simulation was run for a period of 20 days and the plots corresponding to various features such as the growth profile and necrotic core evolution were obtained. These features were compared with the ones observed in other (experimental) studies. One interesting characteristic of our modeling is that it provides us with the ability to predict gene expression patterns through different layers of a tumor, which can have important implications, especially in drug target selection in the field of cancer therapy.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Molecular BioSystems
Molecular BioSystems 生物-生化与分子生物学
CiteScore
2.94
自引率
0.00%
发文量
0
审稿时长
2.6 months
期刊介绍: Molecular Omics publishes molecular level experimental and bioinformatics research in the -omics sciences, including genomics, proteomics, transcriptomics and metabolomics. We will also welcome multidisciplinary papers presenting studies combining different types of omics, or the interface of omics and other fields such as systems biology or chemical biology.
期刊最新文献
Correction: Dynamic properties of dipeptidyl peptidase III from Bacteroides thetaiotaomicron and the structural basis for its substrate specificity – a computational study Pharmacology of predatory and defensive venom peptides in cone snails Staphylococcus aureus extracellular vesicles (EVs): surface-binding antagonists of biofilm formation† Mechanism of the formation of the RecA–ssDNA nucleoprotein filament structure: a coarse-grained approach Conformational heterogeneity in tails of DNA-binding proteins is augmented by proline containing repeats†
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1