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Analysis of a mathematical model for the growth of tumors under the action of external inhibitors

机译:在外部抑制剂作用下肿瘤生长的数学模型的分析

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In this paper we make rigorous analysis to a mathematical model for the growth of nonnecrotic tumors under the action of external inhibitors. By external inhibitor we mean an inhibitor that is either developed from the immune system of the body or administered by medical treatment to distinguish with that secreted by tumor itself. The model modifies a similar model proposed by H. M. Byrne and M. A. J. Chaplain. After simply establishing the well-posedness of the model, we discuss the asymptotic behavior of its solutions by rigorous analysis. The result shows that an evolutionary tumor will finally disappear, or converge to a stationary state (dormant state), or expand unboundedly, depending on which of the four disjoint regions Delta(1), ... ,Delta(4) the parameter vector (A(1), A(2)) belongs to, how large the scaled apoptosis number (σ) over tilde is, and how large the initial radius R-0 of the tumor is. Finally, we discuss some biological implications of the result, which reveals how a tumor varies when inhibitor supply is increased and nutrient supply is reduced. [References: 16]
机译:在本文中,我们对在外部抑制剂作用下非坏死性肿瘤生长的数学模型进行了严格的分析。外部抑制剂是指从机体免疫系统发展而来的抑制剂,或通过药物治疗与肿瘤本身分泌的抑制剂区分开的抑制剂。该模型修改了H. M. Byrne和M. A. J. Chaplain提出的类似模型。简单建立模型的适定性之后,我们通过严格的分析讨论其解的渐近行为。结果表明,根据参数向量四个不相交区域Delta(1),...,Delta(4)中的哪一个,进化肿瘤最终将消失或收敛至静止状态(休眠状态)或无限扩展。 (A(1),A(2))属于,在代字号上缩放的凋亡数(σ)有多大,以及肿瘤的初始半径R-0有多大。最后,我们讨论了该结果的一些生物学含义,揭示了当抑制剂供应增加和营养供应减少时肿瘤如何变化。 [参考:16]

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