ROS1-dependent cancers - biology, diagnostics and therapeutics.

ROS1-dependent cancers - biology, diagnostics and therapeutics.
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DOI:
10.1038/s41571-020-0408-9
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发表时间:
2021-01
期刊:
Nature reviews. Clinical oncology
影响因子:
--
通讯作者:
Davare MA
Davare MA
中科院分区:
其他
文献类型:
--
作者:
Drilon A;Jenkins C;Iyer S;Schoenfeld A;Keddy C;Davare MA

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原癌基因ROS 1编码一种受体酪氨酸激酶,在人类中具有未知的生理作用。涉及ROS 1的体细胞染色体融合产生嵌合癌蛋白,其驱动成人和儿科患者的多种癌症。针对ROS 1的酪氨酸激酶抑制剂(TKI)对这些癌症具有治疗活性,尽管只有早期的多激酶抑制剂获得了监管批准,特别是用于治疗ROS 1融合阳性的非小细胞肺癌;组织学不可知的批准尚未获得批准。患者可能出现对ROS 1 TKI耐药的内在或外在机制。影响耐药性获得的潜在因素包括特定ROS 1癌蛋白的亚细胞定位和TKI特性,如优先参与的激酶构象和ROS 1以外的靶点谱。重要的是,耐药性的多克隆性质仍有待探索。为改善颅内活性和减轻ROS 1内在耐药机制而开发的更高亲和力的下一代ROS 1 TKI已证明在这些方面具有临床疗效,因此突出了序贯ROS 1 TKI治疗的效用。选择性ROS 1抑制剂尚未开发出来,因此ROS 1抑制的特定不良反应无法从可用多激酶抑制剂的毒性特征中去卷积。在此,我们讨论了ROS 1的非恶性和恶性生物学,ROS 1融合存在的诊断挑战以及在治疗初始和获得性耐药环境中靶向ROS 1融合蛋白的策略。
The proto-oncogene ROS1 encodes a receptor tyrosine kinase with an unknown physiological role in humans. Somatic chromosomal fusions involving ROS1 produce chimeric oncoproteins that drive a diverse range of cancers in adult and paediatric patients. ROS1-directed tyrosine kinase inhibitors (TKIs) are therapeutically active against these cancers, although only early-generation multikinase inhibitors have been granted regulatory approval, specifically for the treatment of ROS1 fusion-positive non-small-cell lung cancers; histology-agnostic approvals have yet to be granted. Intrinsic or extrinsic mechanisms of resistance to ROS1 TKIs can emerge in patients. Potential factors that influence resistance acquisition include the subcellular localization of the particular ROS1 oncoprotein and the TKI properties such as the preferential kinase conformation engaged and the spectrum of targets beyond ROS1. Importantly, the polyclonal nature of resistance remains underexplored. Higher-affinity next-generation ROS1 TKIs developed to have improved intracranial activity and to mitigate ROS1-intrinsic resistance mechanisms have demonstrated clinical efficacy in these regards, thus highlighting the utility of sequential ROS1 TKI therapy. Selective ROS1 inhibitors have yet to be developed, and thus the specific adverse effects of ROS1 inhibition cannot be deconvoluted from the toxicity profiles of the available multikinase inhibitors. Herein, we discuss the non-malignant and malignant biology of ROS1, the diagnostic challenges that ROS1 fusions present and the strategies to target ROS1 fusion proteins in both treatment-naive and acquired-resistance settings.
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