Laboratory of Cell Biology, National Cancer Institute, National Institutes of Health, Bethesda, MD 20742, USA.
Drug Resist Updat. 2012 Feb-Apr;15(1-2):90-7. doi: 10.1016/j.drup.2012.01.003. Epub 2012 Mar 3.
Resistance to chemotherapy is a key impediment to successful cancer treatment that has been intensively studied for the last three decades. Several central mechanisms have been identified as contributing to the resistance. In the case of multidrug resistance (MDR), the cell becomes resistant to a variety of structurally and mechanistically unrelated drugs in addition to the drug initially administered. Mathematical models of drug resistance have dealt with many of the known aspects of this field, such as pharmacologic sanctuary and location/diffusion resistance, intrinsic resistance, induced resistance and acquired resistance. In addition, there are mathematical models that take into account the kinetic/phase resistance, and models that investigate intracellular mechanisms based on specific biological functions (such as ABC transporters, apoptosis and repair mechanisms). This review covers aspects of MDR that have been mathematically studied, and explains how, from a methodological perspective, mathematics can be used to study drug resistance. We discuss quantitative approaches of mathematical analysis, and demonstrate how mathematics can be used in combination with other experimental and clinical tools. We emphasize the potential benefits of integrating analytical and mathematical methods into future clinical and experimental studies of drug resistance.
化疗耐药性是成功治疗癌症的主要障碍,过去三十年来,人们对此进行了深入研究。已经确定了几种导致耐药性的核心机制。在多药耐药性 (MDR) 的情况下,细胞不仅对最初给予的药物,而且对多种结构和机制上无关的药物都具有耐药性。耐药性的数学模型已经涉及到该领域的许多已知方面,例如药理避难所和位置/扩散耐药性、内在耐药性、诱导耐药性和获得性耐药性。此外,还有一些数学模型考虑了动力学/相位耐药性,以及基于特定生物学功能(如 ABC 转运蛋白、细胞凋亡和修复机制)的细胞内机制的模型。本综述涵盖了已在数学上进行研究的 MDR 方面,并解释了从方法论的角度来看,如何使用数学来研究耐药性。我们讨论了定量的数学分析方法,并展示了如何将数学与其他实验和临床工具结合使用。我们强调了将分析和数学方法整合到未来的耐药性临床和实验研究中的潜在好处。