Huang Xing, Zhang Gang
Zhejiang Provincial Key Laboratory of Pancreatic Disease, School of Medicine, Zhejiang University, Hangzhou, China.
Front Cell Dev Biol. 2020 Nov 12;8:602352. doi: 10.3389/fcell.2020.602352. eCollection 2020.
Drugs targeting the cyclin-dependent kinase 4/6 (CDK4/6)-retinoblastoma 1 (RB1) axis have shown efficacy against multiple solid cancers, but their therapeutic potential in pancreatic cancer remains poorly defined. A recent report proposed that a "tailored" combination of first-line and second-line CDK4-targeting drugs would hold promise for pancreatic cancer treatment. Indeed, this therapeutic strategy exhibited significantly suppressive effects on pancreatic cancer patient-derived cell lines and tumor tissue . However, the study neglected immune involvement and the influence of CDK6 and RB1 in CDK4 inhibition-based treatment. Herein, we reveal multiple new facets of the CDK4/6-RB1 axis in pancreatic cancer, highlighting the complexity of this signaling axis for future prognostic and therapeutic targeting.
靶向细胞周期蛋白依赖性激酶4/6(CDK4/6)-视网膜母细胞瘤1(RB1)轴的药物已显示出对多种实体癌有效,但它们在胰腺癌中的治疗潜力仍不明确。最近的一份报告提出,一线和二线靶向CDK4药物的“定制”组合有望用于胰腺癌治疗。事实上,这种治疗策略对胰腺癌患者来源的细胞系和肿瘤组织表现出显著的抑制作用。然而,该研究忽略了免疫参与以及CDK6和RB1在基于CDK4抑制的治疗中的影响。在此,我们揭示了胰腺癌中CDK4/6-RB1轴的多个新方面,突出了该信号轴在未来预后和治疗靶向方面的复杂性。