Department of Toxicology and Cancer Biology, University of Kentucky, Lexington, KY, USA.
Department of Mathematics, University of Kentucky, Lexington, KY, USA.
Bull Math Biol. 2023 Aug 30;85(10):89. doi: 10.1007/s11538-023-01197-6.
Modeling cell signal transduction pathways via Boolean networks (BNs) has become an established method for analyzing intracellular communications over the last few decades. What's more, BNs provide a course-grained approach, not only to understanding molecular communications, but also for targeting pathway components that alter the long-term outcomes of the system. This has come to be known as phenotype control theory. In this review we study the interplay of various approaches for controlling gene regulatory networks such as: algebraic methods, control kernel, feedback vertex set, and stable motifs. The study will also include comparative discussion between the methods, using an established cancer model of T-Cell Large Granular Lymphocyte Leukemia. Further, we explore possible options for making the control search more efficient using reduction and modularity. Finally, we will include challenges presented such as the complexity and the availability of software for implementing each of these control techniques.
通过布尔网络 (BNs) 对细胞信号转导途径进行建模,已成为过去几十年中分析细胞内通讯的一种既定方法。更重要的是,BNs 提供了一种粗粒度的方法,不仅可以理解分子通讯,还可以针对改变系统长期结果的途径成分。这被称为表型控制理论。在这篇综述中,我们研究了各种控制基因调控网络的方法的相互作用,如:代数方法、控制核、反馈顶点集和稳定基序。该研究还将包括使用 T 细胞大颗粒淋巴细胞白血病的既定癌症模型对方法进行比较讨论。此外,我们还探索了使用简化和模块化使控制搜索更有效的可能选择。最后,我们将包括提出的挑战,例如复杂性和实施这些控制技术中的每一种的软件可用性。