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A THEORETICAL EXPLANATION OF 'CONCOMITANT RESISTANCE'

机译:“伴随电阻”的理论解释

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Concomitant resistance is a tumor growth dynamic which results when the growth of a second tumor implant is inhibited by the presence of the first. Recently, we modeled tumor growth in the presence of a regenerating liver after partial hepatectomy (Michelson and Leith, Bull. Math. Biol. 57, 345-366, 1995), with an interlocking pair of growth control triads to account for the accelerated growth observed in both tissues. We also modeled tumor dormancy and recurrence as a dynamic equilibrium achieved between proliferating and quiescent subpopulations. In this paper those studies are extended to initially model the concomitant resistance case. Two interlocking model systems are proposed. In one an interactive competition between the tumor implants is described, while in the other purely proportional growth inhibition is described. The equilibria and dynamics of each system when the coefficients are held constant are presented for three subcases of model parameters. We show that the dynamic called concomitant resistance can be real or apparent, and that if the model coefficients are held constant, the only way to truly achieve concomitant resistance is by forcing one of the tumors into total quiescence. If this is the true state of the inhibited implant, then a non-constant recruitment signal is required to insure regrowth when the inhibitor mass is excised. We compare these theoretical results to a potential explanation of the phenomenon provided by Prehn.
机译:伴随的抗性是当第二肿瘤植入物的生长被第一个肿瘤植入物的生长抑制时导致的肿瘤生长动力学。最近,我们模拟了部分肝切除术后再生肝脏存在下的肿瘤生长情况(Michelson和Leith,Bull。Math。Biol。57,345-366,1995),其中有一对联锁的生长控制三联体以说明加速的生长在两个组织中观察到。我们还将肿瘤休眠和复发建模为增殖和静态亚群之间实现的动态平衡。在本文中,这些研究已扩展到最初对伴随抵抗的情况进行建模。提出了两个互锁模型系统。一种描述了肿瘤植入物之间的相互作用,而另一种描述了纯比例生长抑制。对于模型参数的三个子情况,给出了当系数保持恒定时每个系统的平衡和动力学。我们表明,动态的所谓伴随耐药性可以是真实的或明显的,并且如果模型系数保持恒定,则要真正实现伴随耐药性的唯一方法是迫使其中一个肿瘤完全静止。如果这是被抑制的植入物的真实状态,则在切除抑制物质量时需要非恒定的募集信号以确保再生。我们将这些理论结果与Prehn提供的现象的潜在解释进行了比较。

著录项

  • 来源
    《Bulletin of Mathematical Biology》 |1995年第5期|p.733-747|共15页
  • 作者

    SETH MICHELSON; JOHN T. LEITH;

  • 作者单位

    Department of Biomathematics, Scientific Information Services, Syntex Drug Discovery Research, 3401 Hillview Avenue, Palo Alto, CA 94393, U.S.A.;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 普通生物学;
  • 关键词

  • 入库时间 2022-08-18 00:19:57

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