The molecular determinants of phenotypic plasticity in homeostasis and neoplasia.

Cancer heterogeneity and plasticity Pub Date : 2024-01-01 Epub Date: 2024-12-13 DOI:10.47248/chp2401020010
Bradley Balk, David W Goodrich
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引用次数: 0

Abstract

Phenotypic plasticity, the capacity of cells to transition between distinct phenotypic and lineage states over time, is a genetically and epigenetically encoded trait essential for normal development and adult tissue homeostasis. In cancer, phenotypic plasticity programs can be deployed aberrantly to enable disease progression and acquired therapeutic resistance. Cancer phenotypic plasticity is a current barrier to achieving cures for advanced cancers using available molecularly targeted therapies. This review summarizes the complex and interconnected molecular pathways implicated in phenotypic plasticity, both in the context of normal tissue homeostasis and cancer. Molecular pathways convergent between these contexts are highlighted while pathways enabling plasticity are distinguished from those that specify the phenotype of already plastic cells. Key unresolved questions in the field are discussed along with emerging technologies that may be used to help answer them.

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内稳态和肿瘤中表型可塑性的分子决定因素。
表型可塑性是细胞随时间在不同表型和谱系状态之间转换的能力,是正常发育和成人组织稳态所必需的遗传和表观遗传编码特征。在癌症中,表型可塑性程序可以异常地部署,使疾病进展和获得治疗耐药性。癌症表型可塑性是目前使用分子靶向治疗实现晚期癌症治疗的障碍。这篇综述总结了在正常组织稳态和癌症的背景下,涉及表型可塑性的复杂和相互关联的分子途径。在这些背景之间的分子途径被强调,而使可塑性的途径与那些指定已经塑性细胞表型的途径是区分开来的。讨论了该领域尚未解决的关键问题,以及可能用于帮助回答这些问题的新兴技术。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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