CDK12在人类癌症中作用的新见解:癌症治疗的机制和干预措施。

IF 8.9
Journal of pharmaceutical analysis Pub Date : 2025-07-01 Epub Date: 2024-12-28 DOI:10.1016/j.jpha.2024.101173
Wei Dai, Dong Xie, Hao Huang, Jingxuan Li, Caiyao Guo, Fuqiang Cao, Luo Yang, Chengyong Zhong, Shenglan Liu
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引用次数: 0

摘要

细胞周期蛋白依赖性激酶12 (CDK12)的失调可能是由基因组改变或上游效应物的调节引起的,与癌症的发生和进展有关。CDK12过表达或激活足以诱导肿瘤的发生、复发和治疗抵抗。然而,CDK12也可能以上下文依赖的方式发挥肿瘤抑制功能。因此,在未来的临床试验中,靶向CDK12是有必要谨慎的。全面阐明CDK12在肿瘤发生中的双重作用和潜在机制,是推进精准肿瘤学的迫切需要。本文综述了目前对CDK12在癌症中的失调和生物学作用的理解。随后,我们系统地总结了CDK12在不同背景下的致癌和抑瘤作用的功能和机制。最后,我们讨论了CDK12作为一种新的治疗靶点的潜力及其在临床肿瘤学中的意义,为创新癌症治疗策略的未来方向提供了见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
New insights into the dule roles CDK12 in human cancers: Mechanisms and interventions for cancer therapy.

The dysregulation of cyclin-dependent kinase 12 (CDK12), which may result from genomic alterations or modulation by upstream effectors, is implicated in cancer oncogenesis and progression. CDK12 overexpression or activation is sufficient to induce tumor initiation, recurrence, and therapeutic resistance. However, CDK12 may also exert tumor-suppressive functions in a context-dependent manner. Therefore, caution is warranted when targeting CDK12 in future clinical trials. A comprehensive elucidation of the dual roles and underlying mechanisms of CDK12 in carcinogenesis is urgently needed to advance precision oncology. This review provides an overview of the current understanding of the dysregulation and biological roles of CDK12 in cancer. Subsequently, we systematically summarize the functions and mechanisms of the oncogenic and tumor-suppressive roles of CDK12 in different contexts. Finally, we discuss the potential of CDK12 as a novel therapeutic target and its implications in clinical oncology, offering insights into future directions for innovative cancer treatment strategies.

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