RB1, Cancer Lineage Plasticity, and Therapeutic Resistance

Letian Zhang, David W. Goodrich
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Abstract

Lineage plasticity, a cell's capacity to switch lineage-restricted gene expression states, is required for normal tissue homeostasis. Cancer lineage plasticity is increasingly observed as a mechanism of resistance to therapy, particularly molecularly targeted therapies. These therapies often owe their superior efficacy to the lineage-restricted nature of their therapeutic target, so cancers can evade such therapies by changing lineage states. As increasingly effective molecularly targeted therapies are deployed, cancer lineage plasticity is likely to be a growing clinical problem. Lineage plasticity reflects a nongenetic, potentially reversible transcriptional adaptation, but oncogenic genetic mutations likely drive elevated lineage plasticity that is typical of cancer cells. Here key concepts relevant to cancer lineage plasticity are presented, evidence implicating loss of the RB1 tumor-suppressor gene in driving cancer lineage plasticity is reviewed, and possible therapeutic approaches to counter cancer lineage plasticity are discussed.
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RB1,肿瘤谱系可塑性和治疗耐药性
谱系可塑性是细胞转换谱系限制基因表达状态的能力,是正常组织稳态所必需的。癌症谱系可塑性越来越多地被认为是一种抵抗治疗的机制,特别是分子靶向治疗。这些疗法通常将其优越的疗效归功于其治疗靶点的谱系限制性质,因此癌症可以通过改变谱系状态来逃避这些疗法。随着越来越有效的分子靶向治疗的部署,癌症谱系可塑性可能是一个日益严重的临床问题。谱系可塑性反映了一种非遗传的、潜在可逆的转录适应,但致癌基因突变可能会提高谱系可塑性,这是癌细胞的典型特征。本文介绍了与癌症谱系可塑性相关的关键概念,综述了RB1肿瘤抑制基因缺失在驱动癌症谱系可塑性中的证据,并讨论了对抗癌症谱系可塑性的可能治疗方法。
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