Division of Hygienic Chemistry, Faculty of Pharmacy, Keio University, 1-5-30 Shibakoen, Minato-ku, Tokyo 105-8512, Japan.
Division of Structural Biochemistry, Department of Biochemistry, Jichi Medical University, Shimotsuke 321-0498, Japan.
Int J Mol Sci. 2022 Jan 11;23(2):749. doi: 10.3390/ijms23020749.
In the treatment of breakpoint cluster region-Abelson (BCR-ABL)-positive chronic myeloid leukemia (CML) using BCR-ABL inhibitors, the appearance of a gatekeeper mutation (T315I) in BCR-ABL is a serious issue. Therefore, the development of novel drugs that overcome acquired resistance to BCR-ABL inhibitors by CML cells is required. We previously demonstrated that a bis-pyridinium fullerene derivative (BPF) induced apoptosis in human chronic myeloid leukemia (CML)-derived K562 cells partially through the generation of reactive oxygen species (ROS). We herein show that BPF enhanced the activation of the mitogen-activated protein kinase/extracellular signal-regulated kinase kinase-extracellular signal-regulated kinase (MEK-ERK) pathway in a ROS-independent manner. BPF-induced apoptosis was attenuated by trametinib, suggesting the functional involvement of the MEK-ERK pathway in apoptosis in K562 cells. In addition, the constitutive activation of the MEK-ERK pathway by the enforced expression of the BRAFV600E mutant significantly increased the sensitivity of K562 cells to BPF. These results confirmed for the first time that BPF induces apoptosis in K562 cells through dual pathways-ROS production and the activation of the MEK-ERK pathway. Furthermore, BPF induced cell death in transformed Ba/F3 cells expressing not only BCR-ABL but also T315I mutant through the activation of the MEK-ERK pathway. These results indicate that BPF is as an effective CML drug that overcomes resistance to BCR-ABL inhibitors.
在使用 BCR-ABL 抑制剂治疗 BCR-ABL 阳性慢性髓性白血病(CML)时,BCR-ABL 中出现看门突变(T315I)是一个严重的问题。因此,需要开发新型药物来克服 CML 细胞对 BCR-ABL 抑制剂的获得性耐药。我们之前证明,双吡啶富勒烯衍生物(BPF)通过生成活性氧物种(ROS)部分诱导人慢性髓性白血病(CML)衍生的 K562 细胞凋亡。我们在此表明,BPF 以 ROS 非依赖性方式增强丝裂原活化蛋白激酶/细胞外信号调节激酶激酶-细胞外信号调节激酶(MEK-ERK)途径的激活。BPF 诱导的细胞凋亡被 trametinib 减弱,表明 MEK-ERK 途径在 K562 细胞凋亡中具有功能。此外,通过强制表达 BRAFV600E 突变体使 MEK-ERK 途径持续激活,显著增加了 K562 细胞对 BPF 的敏感性。这些结果首次证实 BPF 通过产生 ROS 和激活 MEK-ERK 途径这两种途径诱导 K562 细胞凋亡。此外,BPF 通过激活 MEK-ERK 途径诱导不仅表达 BCR-ABL 而且还表达 T315I 突变体的转化的 Ba/F3 细胞死亡。这些结果表明,BPF 是一种有效的 CML 药物,可克服对 BCR-ABL 抑制剂的耐药性。