Department of Thyroid and Breast Surgery, Ningbo Medical Centre, the Affiliated Lihuili Hospital of Ningbo University, Ningbo.
Department of Electronic Commerce, Zhejiang Fashion Institute of Technology, Ningbo.
Bioengineered. 2022 May;13(5):12888-12898. doi: 10.1080/21655979.2022.2078557.
The mitogen-activated protein kinase kinase 5 (MEK5)/extracellular signal-regulated kinase 5 (ERK5) axis has been reported to promote tumorigenesis in breast cancer (BC). Therefore, targeting the MEK5/ERK5 axis is a potential strategy against BC. BAY-885 is a novel inhibitor of ERK5; however, to date, its anti-tumor effects in BC have not been investigated. This study aimed to assess the anti-tumor effects of BAY-885 in BC and identify its underlying mechanisms of action. Unlike other ERK5 inhibitors, which frequently failed to mimic ERK5 genetic ablation phenotypes, the BAY-885 treatment effectively recapitulated ERK5 depletion effects in BC cells. Results revealed that BAY-885 affected the viability and induced apoptosis in BC cells. Moreover, the BAY-885-mediated downregulation of myeloid cell leukemia-1 (Mcl-1) and upregulation of Bim were dependent on ERK5 inhibition. Furthermore, BAY-885 triggered activation of endoplasmic reticulum (ER) stress, which further led to the upregulation of Bim and downregulation of Mcl-1. ER stress was induced in an ERK5 inhibition-dependent manner. These findings suggested that BAY-885 induced apoptosis in BC cells via ER stress/Mcl-1/Bim axis, suggesting that BAY-885 may serve as a therapeutic agent for BC.
丝裂原活化蛋白激酶激酶 5(MEK5)/细胞外信号调节激酶 5(ERK5)轴已被报道可促进乳腺癌(BC)的肿瘤发生。因此,靶向 MEK5/ERK5 轴是一种针对 BC 的潜在策略。BAY-885 是一种新型 ERK5 抑制剂;然而,迄今为止,其在 BC 中的抗肿瘤作用尚未得到研究。本研究旨在评估 BAY-885 在 BC 中的抗肿瘤作用,并确定其作用机制。与其他经常无法模拟 ERK5 基因缺失表型的 ERK5 抑制剂不同,BAY-885 治疗有效地再现了 BAY-885 在 BC 细胞中对 ERK5 的耗竭作用。结果表明,BAY-885 影响 BC 细胞的活力并诱导其凋亡。此外,BAY-885 介导的髓样细胞白血病-1(Mcl-1)下调和 Bim 上调依赖于 ERK5 抑制。此外,BAY-885 触发内质网(ER)应激的激活,进而导致 Bim 的上调和 Mcl-1 的下调。ERK5 抑制依赖性地诱导 ER 应激。这些发现表明,BAY-885 通过 ER 应激/Mcl-1/Bim 轴诱导 BC 细胞凋亡,表明 BAY-885 可能作为 BC 的治疗剂。