异质性肿瘤细胞群的随机药效学研究。

IF 2.2 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Van Thuy Truong, Paolo Vicini, James Yates, Vincent Dubois, Grant Lythe
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引用次数: 0

摘要

标准药效学模型为常微分方程,不具有随机性和异质性。我们开发并分析了用药物治疗的异质性肿瘤细胞群的随机模型,其中每个细胞具有与生存相关的不同属性值。一旦药物将细胞的值降低到阈值以下,细胞就容易死亡。种群中最后一个细胞的消除是确定性模型中不可用的自然终点。我们在一组肿瘤细胞中找到了这种消失时间的概率密度公式,在药物的影响下,每个肿瘤细胞都有不同的调节值。肿瘤种群大小与平均灭绝时间呈对数关系。我们还分析了重复用药剂量下的人群和随后的恢复情况。随机细胞死亡和分裂事件(以及相关的机制参数)决定了细胞群体的最终命运。我们确定了将长期肿瘤人口增长与成功的多剂量治疗分开的临界分裂率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Stochastic pharmacodynamics of a heterogeneous tumour-cell population.

Standard pharmacodynamic models are ordinary differential equations without the features of stochasticity and heterogeneity. We develop and analyse a stochastic model of a heterogeneous tumour-cell population treated with a drug, where each cell has a different value of an attribute linked to survival. Once the drug reduces a cell's value below a threshold, the cell is susceptible to death. The elimination of the last cell in the population is a natural endpoint that is not available in deterministic models. We find formulae for the probability density of this extinction time in a collection of tumour cells, each with a different regulator value, under the influence of a drug. There is a logarithmic relationship between tumour population size and mean time to extinction. We also analyse the population under repeated drug doses and subsequent recoveries. Stochastic cell death and division events (and the relevant mechanistic parameters) determine the ultimate fate of the cell population. We identify the critical division rate separating long-term tumour population growth from successful multiple-dose treatment.

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来源期刊
CiteScore
4.90
自引率
4.00%
发文量
39
审稿时长
6-12 weeks
期刊介绍: Broadly speaking, the Journal of Pharmacokinetics and Pharmacodynamics covers the area of pharmacometrics. The journal is devoted to illustrating the importance of pharmacokinetics, pharmacodynamics, and pharmacometrics in drug development, clinical care, and the understanding of drug action. The journal publishes on a variety of topics related to pharmacometrics, including, but not limited to, clinical, experimental, and theoretical papers examining the kinetics of drug disposition and effects of drug action in humans, animals, in vitro, or in silico; modeling and simulation methodology, including optimal design; precision medicine; systems pharmacology; and mathematical pharmacology (including computational biology, bioengineering, and biophysics related to pharmacology, pharmacokinetics, orpharmacodynamics). Clinical papers that include population pharmacokinetic-pharmacodynamic relationships are welcome. The journal actively invites and promotes up-and-coming areas of pharmacometric research, such as real-world evidence, quality of life analyses, and artificial intelligence. The Journal of Pharmacokinetics and Pharmacodynamics is an official journal of the International Society of Pharmacometrics.
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