Dai Wei, Xie Dong, Huang Hao, Li Jingxuan, Guo Caiyao, Cao Fuqiang, Yang Luo, Zhong Chengyong, Liu Shenglan
Jiangxi Province Key Laboratory of Pharmacology of Traditional Chinese Medicine, School of Pharmacy, Gannan Medical University, Ganzhou, Jiangxi, 341000, China.
Key Laboratory of Prevention and Treatment of Cardiovascular and Cerebrovascular Diseases, Ministry of Education, Jiangxi Provincial Key Laboratory of Tissue Engineering, School of Rehabilitation Medicine, Gannan Medical University, Ganzhou, Jiangxi, 341000, China.
J Pharm Anal. 2025 Jul;15(7):101173. doi: 10.1016/j.jpha.2024.101173. Epub 2024 Dec 28.
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.
细胞周期蛋白依赖性激酶12(CDK12)的失调可能源于基因组改变或上游效应器的调节,与癌症的发生和进展有关。CDK12的过表达或激活足以诱导肿瘤起始、复发和治疗抗性。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时需要谨慎。迫切需要全面阐明CDK12在致癌作用中的双重作用和潜在机制,以推进精准肿瘤学。本综述概述了目前对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肿瘤抑制作用的功能和机制。最后,我们讨论了CDK12作为新型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见解。