作为癌症模型的囚徒困境。

Convergent science physical oncology Pub Date : 2016-09-01 Epub Date: 2016-07-04 DOI:10.1088/2057-1739/2/3/035002
Jeffrey West, Zaki Hasnain, Jeremy Mason, Paul K Newton
{"title":"作为癌症模型的囚徒困境。","authors":"Jeffrey West, Zaki Hasnain, Jeremy Mason, Paul K Newton","doi":"10.1088/2057-1739/2/3/035002","DOIUrl":null,"url":null,"abstract":"<p><p>Tumor development is an evolutionary process in which a heterogeneous population of cells with different growth capabilities compete for resources in order to gain a proliferative advantage. What are the minimal ingredients needed to recreate some of the emergent features of such a developing complex ecosystem? What is a tumor doing before we can detect it? We outline a mathematical model, driven by a stochastic Moran process, in which cancer cells and healthy cells compete for dominance in the population. Each are assigned payoffs according to a Prisoner's Dilemma evolutionary game where the healthy cells are the cooperators and the cancer cells are the defectors. With point mutational dynamics, heredity, and a fitness landscape controlling birth and death rates, natural selection acts on the cell population and simulated 'cancer-like' features emerge, such as Gompertzian tumor growth driven by heterogeneity, the log-kill law which (linearly) relates therapeutic dose density to the (log) probability of cancer cell survival, and the Norton-Simon hypothesis which (linearly) relates tumor regression rates to tumor growth rates. We highlight the utility, clarity, and power that such models provide, despite (and because of) their simplicity and built-in assumptions.</p>","PeriodicalId":91466,"journal":{"name":"Convergent science physical oncology","volume":"2 3","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2016-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5701760/pdf/nihms913703.pdf","citationCount":"0","resultStr":"{\"title\":\"The prisoner's dilemma as a cancer model.\",\"authors\":\"Jeffrey West, Zaki Hasnain, Jeremy Mason, Paul K Newton\",\"doi\":\"10.1088/2057-1739/2/3/035002\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Tumor development is an evolutionary process in which a heterogeneous population of cells with different growth capabilities compete for resources in order to gain a proliferative advantage. What are the minimal ingredients needed to recreate some of the emergent features of such a developing complex ecosystem? What is a tumor doing before we can detect it? We outline a mathematical model, driven by a stochastic Moran process, in which cancer cells and healthy cells compete for dominance in the population. Each are assigned payoffs according to a Prisoner's Dilemma evolutionary game where the healthy cells are the cooperators and the cancer cells are the defectors. With point mutational dynamics, heredity, and a fitness landscape controlling birth and death rates, natural selection acts on the cell population and simulated 'cancer-like' features emerge, such as Gompertzian tumor growth driven by heterogeneity, the log-kill law which (linearly) relates therapeutic dose density to the (log) probability of cancer cell survival, and the Norton-Simon hypothesis which (linearly) relates tumor regression rates to tumor growth rates. We highlight the utility, clarity, and power that such models provide, despite (and because of) their simplicity and built-in assumptions.</p>\",\"PeriodicalId\":91466,\"journal\":{\"name\":\"Convergent science physical oncology\",\"volume\":\"2 3\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2016-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5701760/pdf/nihms913703.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Convergent science physical oncology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1088/2057-1739/2/3/035002\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2016/7/4 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Convergent science physical oncology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1088/2057-1739/2/3/035002","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2016/7/4 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

肿瘤的发展是一个进化过程,在这一过程中,具有不同生长能力的异质细胞群为获得增殖优势而争夺资源。要重现这样一个发展中的复杂生态系统的某些突发特征,需要哪些最基本的成分?在我们检测到肿瘤之前,它在做什么?我们概述了一个由随机莫兰过程驱动的数学模型,在这个模型中,癌细胞和健康细胞为争夺群体中的优势地位而竞争。根据 "囚徒困境 "进化博弈,健康细胞是合作者,而癌细胞是叛逃者,两者各自分配报酬。通过点突变动态、遗传和控制出生率和死亡率的适应度景观,自然选择作用于细胞群,模拟出 "类癌 "特征,如异质性驱动的冈pertz肿瘤生长、将治疗剂量密度与癌细胞存活概率(对数)线性关联的对数致死定律,以及将肿瘤消退率与肿瘤生长率线性关联的诺顿-西蒙假说。我们强调了这些模型的实用性、清晰度和强大功能,尽管(也正因为)它们很简单,而且有内置假设。
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

摘要图片

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
The prisoner's dilemma as a cancer model.

Tumor development is an evolutionary process in which a heterogeneous population of cells with different growth capabilities compete for resources in order to gain a proliferative advantage. What are the minimal ingredients needed to recreate some of the emergent features of such a developing complex ecosystem? What is a tumor doing before we can detect it? We outline a mathematical model, driven by a stochastic Moran process, in which cancer cells and healthy cells compete for dominance in the population. Each are assigned payoffs according to a Prisoner's Dilemma evolutionary game where the healthy cells are the cooperators and the cancer cells are the defectors. With point mutational dynamics, heredity, and a fitness landscape controlling birth and death rates, natural selection acts on the cell population and simulated 'cancer-like' features emerge, such as Gompertzian tumor growth driven by heterogeneity, the log-kill law which (linearly) relates therapeutic dose density to the (log) probability of cancer cell survival, and the Norton-Simon hypothesis which (linearly) relates tumor regression rates to tumor growth rates. We highlight the utility, clarity, and power that such models provide, despite (and because of) their simplicity and built-in assumptions.

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
自引率
0.00%
发文量
0
期刊最新文献
Time for a change: considering the rights of study participants to ownership of their personal research-grade genomic data Meeting report: The physics of life—merging clinical, biological and physical sciences approaches for cancer research Changing cell mechanics—a precondition for malignant transformation of oral squamous carcinoma cells Heterogeneous radiotherapy dose-outcomes response in parotid glands Secondary use of electronic medical records for clinical research: Challenges and Opportunities.
×
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