Caroland Kailey, Shi Changyou, Lin Jiayuh
Department of Biochemistry and Molecular Biology, School of Medicine, University of Maryland, Baltimore, MD 21201, USA.
Oncol Lett. 2024 Sep 19;28(6):554. doi: 10.3892/ol.2024.14688. eCollection 2024 Dec.
Triple-negative breast cancer (TNBC) is an aggressive disease with the capability of metastasizing quickly. However, treatment options for patients with TNBC still remain limited. CDK4/6 inhibitors have been approved by the U.S. Food and Drug Administration and are administered for the treatment of hormone receptor-positive breast cancer subtypes, but not yet for TNBC. Although pre-clinical research is being conducted on their efficacy in treating TNBC, acquired resistance to CDK4/6 inhibitors is now a growing clinical problem. One of the identified resistance mechanisms is through the IL-6/STAT3 signaling pathway. In the present study, the CDK4/6 inhibitor, abemaciclib, was tested in combination with the IL-6 inhibitor, bazedoxifene, on human (SUM159 and MDA-MB-231) and murine (4T1) TNBC cell lines. Both abemaciclib and bazedoxifene monotherapies inhibited cell cycle progression and cell viability, migration and invasion, and induced apoptosis; however, the combination treatment exerted a greater effect than either monotherapy. These findings support the concept of CDK4/6 and IL-6 dual inhibition as a novel targeted therapy against TNBC.
三阴性乳腺癌(TNBC)是一种侵袭性疾病,具有快速转移的能力。然而,TNBC患者的治疗选择仍然有限。细胞周期蛋白依赖性激酶4/6(CDK4/6)抑制剂已获美国食品药品监督管理局批准,用于治疗激素受体阳性乳腺癌亚型,但尚未用于TNBC。尽管目前正在进行关于其治疗TNBC疗效的临床前研究,但对CDK4/6抑制剂获得性耐药现已成为一个日益严重的临床问题。已确定的耐药机制之一是通过白细胞介素-6(IL-6)/信号转导和转录激活因子3(STAT3)信号通路。在本研究中,对CDK4/6抑制剂阿贝西利与IL-6抑制剂巴泽昔芬联合用药,在人(SUM159和MDA-MB-231)和小鼠(4T1)TNBC细胞系上进行了测试。阿贝西利和巴泽昔芬单药治疗均抑制细胞周期进程、细胞活力、迁移和侵袭,并诱导细胞凋亡;然而,联合治疗比任何一种单药治疗都具有更大的效果。这些发现支持了CDK4/6和IL-6双重抑制作为一种针对TNBC的新型靶向治疗的概念。