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一种由血管内皮生长因子和血管生成素调节的肿瘤血管生成数学模型。

A mathematical model of tumour angiogenesis, regulated by vascular endothelial growth factor and the angiopoietins.

作者信息

Plank M J, Sleeman B D, Jones P F

机构信息

School of Mathematics, University of Leeds, Leeds LS2 9JT, UK.

出版信息

J Theor Biol. 2004 Aug 21;229(4):435-54. doi: 10.1016/j.jtbi.2004.04.012.

Abstract

Angiogenesis--the growth of new blood vessels from existing ones--is a prerequisite for the growth of solid tumours beyond a diameter of approximately 2 mm. In recent years, the angiopoietins have emerged as important regulators of angiogenesis. They mediate a delicate balance between vascular quiescence, regression and new growth, but their mechanism of action is not fully understood. This work attempts to provide a mathematical description of the role of the angiopoietins in angiogenesis. The model is formulated within the framework of reinforced random walks, which allows easy transition between the continuum (macroscopic) and discrete (microscopic) forms. Model predictions are in qualitative agreement with experimental observations, and may have implications for anti-cancer therapies based on the prevention of angiogenesis.

摘要

血管生成——即从现有血管生长出新的血管——是实体肿瘤生长超过约2毫米直径的先决条件。近年来,血管生成素已成为血管生成的重要调节因子。它们介导血管静止、消退和新生长之间的微妙平衡,但其作用机制尚未完全了解。这项工作试图对血管生成素在血管生成中的作用提供一个数学描述。该模型是在强化随机游走的框架内制定的,这使得在连续(宏观)和离散(微观)形式之间能够轻松转换。模型预测与实验观察结果在定性上一致,并且可能对基于预防血管生成的抗癌疗法有影响。

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