Predicting mechanism of biphasic growth factor action on tumor growth using a multi-species model with feedback control.

Anna Konstorum, Stephanie A Sprowl, Marian L Waterman, Arthur D Lander, John S Lowengrub
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Abstract

A large number of growth factors and drugs are known to act in a biphasic manner: at lower concentrations they cause increased division of target cells, whereas at higher concentrations the mitogenic effect is inhibited. Often, the molecular details of the mitogenic effect of the growth factor are known, whereas the inhibitory effect is not. Hepatoctyte Growth Factor, HGF, has recently been recognized as a strong mitogen that is present in the microenvironment of solid tumors. Recent evidence suggests that HGF acts in a biphasic manner on tumor growth. We build a multi-species model of HGF action on tumor cells using different hypotheses for high dose-HGF activation of a growth inhibitor and show that the shape of the dose-response curve is directly related to the mechanism of inhibitor activation. We thus hypothesize that the shape of a dose-response curve is informative of the molecular action of the growth factor on the growth inhibitor.

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利用带反馈控制的多物种模型预测双相生长因子对肿瘤生长的作用机制
众所周知,许多生长因子和药物都以双相方式发挥作用:浓度较低时,它们会导致目标细胞的分裂增加,而浓度较高时,其促有丝分裂作用会受到抑制。通常,生长因子有丝分裂作用的分子细节是已知的,而抑制作用则不为人知。肝细胞生长因子(HGF)最近被认为是一种存在于实体瘤微环境中的强有丝分裂原。最近的证据表明,HGF 对肿瘤生长的作用是双相的。我们利用高剂量 HGF 激活生长抑制剂的不同假设,建立了一个 HGF 对肿瘤细胞作用的多物种模型,结果表明剂量-反应曲线的形状与抑制剂的激活机制直接相关。因此我们假设,剂量反应曲线的形状可以说明生长因子对生长抑制剂的分子作用。
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