Department of Human Anatomy and Cell Sciences, University of Manitoba, Max Rady College of Medicine, Winnipeg, Manitoba, Canada; Electrophysiology Research Center, Neuroscience Institute, Tehran University of Medical Sciences, Tehran, Iran.
Department of Human Anatomy and Cell Sciences, University of Manitoba, Max Rady College of Medicine, Winnipeg, Manitoba, Canada.
Biochim Biophys Acta Mol Basis Dis. 2024 Oct;1870(7):167332. doi: 10.1016/j.bbadis.2024.167332. Epub 2024 Jul 1.
Malignant cell plasticity is an important hallmark of tumor biology and crucial for metastasis and resistance. Cell plasticity lets cancer cells adapt to and escape the therapeutic strategies, which is the leading cause of cancer patient mortality. Epithelial cells acquire mobility via epithelial-mesenchymal transition (EMT), whereas mesenchymal cells enhance their migratory ability and clonogenic potential by acquiring amoeboid characteristics through mesenchymal-amoeboid transition (MAT). Tumor formation, progression, and metastasis depend on the tumor microenvironment (TME), a complex ecosystem within and around a tumor. Through increased migration and metastasis of cancer cells, the TME also contributes to malignancy. This review underscores the distinction between invasion pattern morphological manifestations and the diverse structures found within the TME. Furthermore, the mechanisms by which amoeboid-associated characteristics promote resistance and metastasis and how these mechanisms may represent therapeutic opportunities are discussed.
恶性细胞可塑性是肿瘤生物学的一个重要标志,对于转移和耐药性至关重要。细胞可塑性使癌细胞能够适应和逃避治疗策略,这是癌症患者死亡的主要原因。上皮细胞通过上皮-间充质转化(EMT)获得迁移能力,而间充质细胞通过获得阿米巴样特征通过间充质-阿米巴样转化(MAT)增强其迁移能力和克隆形成能力。肿瘤的形成、进展和转移依赖于肿瘤微环境(TME),这是肿瘤内和周围的一个复杂生态系统。通过增加癌细胞的迁移和转移,TME 也促进了恶性肿瘤的发生。本综述强调了侵袭模式形态表现与 TME 内发现的不同结构之间的区别。此外,还讨论了阿米巴样相关特征促进耐药性和转移的机制,以及这些机制如何成为治疗机会。