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巴泽昔芬与阿贝西利联合治疗对三阴性乳腺癌细胞的体外协同作用。

Synergistic effect of bazedoxifene and abemaciclib co‑treatment in triple‑negative breast cancer cells in vitro.

作者信息

Caroland Kailey, Shi Changyou, Lin Jiayuh

机构信息

Department of Biochemistry and Molecular Biology, School of Medicine, University of Maryland, Baltimore, MD 21201, USA.

出版信息

Oncol Lett. 2024 Sep 19;28(6):554. doi: 10.3892/ol.2024.14688. eCollection 2024 Dec.

DOI:10.3892/ol.2024.14688
PMID:39355786
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11443307/
Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb12/11443307/a56790e6b35e/ol-28-06-14688-g05.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb12/11443307/b47a1318a676/ol-28-06-14688-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb12/11443307/c8d1be9470a0/ol-28-06-14688-g02.jpg
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本文引用的文献

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Open-label, phase II, multicenter study of lasofoxifene plus abemaciclib for treating women with metastatic ER+/HER2- breast cancer and an ESR1 mutation after disease progression on prior therapies: ELAINE 2.一项关于拉索昔芬联合阿贝西利治疗既往治疗后疾病进展的伴有ESR1突变的转移性ER+/HER2-乳腺癌女性患者的开放标签、II期、多中心研究:ELAINE 2。
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CDK4/6 inhibitors: mechanisms of resistance and potential biomarkers of responsiveness in breast cancer.CDK4/6抑制剂:乳腺癌中的耐药机制及反应性潜在生物标志物
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