癌症转移动力学的计算建模、机器学习和图像分析综述

Shreyas U. Hirway, Seth H. Weinberg
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引用次数: 0

摘要

癌症是一种危及生命的过程,源于细胞中的基因突变,导致肿瘤的形成,是美国死亡的主要原因,继发性转移是死亡的主要驱动因素。最佳转移环境的形成是肿瘤转移前必不可少的过程。这个过程被称为转移前生态位形成,涉及到常驻成纤维细胞样细胞和巨噬细胞的激活。引入这种环境的肿瘤介导因子转化驻留细胞,分泌额外的生长因子并重塑细胞外基质,这被认为促进肿瘤在继发性环境中的定植和转移。此外,转移的一个重要组成部分是上皮-间质转化的生物学过程,癌细胞可以利用这一过程改变其表型,根据需要进行迁移和增殖。在这篇综述中,我们讨论了癌症生长和迁移研究的最新进展。计算模型的重点是生化信号和多细胞动力学检查。还探讨了机器学习模型和分类癌症相关数据的图像分析。通过这篇综述,我们重点介绍了癌症和转移信号的重要方面的研究进展以及研究这些动态的计算工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A review of computational modeling, machine learning and image analysis in cancer metastasis dynamics

A review of computational modeling, machine learning and image analysis in cancer metastasis dynamics

Cancer is a life-threatening process that stems from genetic mutations in cells, which leads to the formation of tumors, and is a major cause of deaths in the United States, with secondary metastasis being a major driver of fatality. The development of an optimal metastatic environment is an essential process prior to tumor metastasis. This process, called pre-metastatic niche formation, involves the activation of resident fibroblast-like cells and macrophages. Tumor-mediated factors introduced to this environment transform resident cells that secrete additional growth factors and remodel the extracellular matrix, which is thought to promote tumor colonization and metastasis in the secondary environment. Furthermore, an important component of metastasis is the biological process of epithelial–mesenchymal transition, which can be exploited by cancer cells to change their phenotype, to migrate and proliferate as necessary. In this review, we discuss recent advances in the investigation of cancer growth and migration. Computational models that focus on biochemical signaling and multicellular dynamics are examined. Machine learning models and image analysis that classify cancer-related data are also explored. Through this review, we highlight advances in the study of important aspects of cancer and metastasis signaling and computational tools to study these dynamics.

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CiteScore
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