UNIPRO-Oral Pathology and Rehabilitation Research Unit, University Institute of Health Sciences (IUCS), CESPU, Rua Central de Gandra, 1317, 4585-116 Gandra, Portugal.
Faculty of Sciences, University of Porto, Rua do Campo Alegre, s/n, 4169-007 Porto, Portugal.
Molecules. 2021 Nov 25;26(23):7139. doi: 10.3390/molecules26237139.
Previously, we reported the in vitro growth inhibitory effect of diarylpentanoid BP-M345 on human cancer cells. Nevertheless, at that time, the cellular mechanism through which BP-M345 exerts its growth inhibitory effect remained to be explored. In the present work, we report its mechanism of action on cancer cells. The compound exhibits a potent tumor growth inhibitory activity with high selectivity index. Mechanistically, it induces perturbation of the spindles through microtubule instability. As a consequence, treated cells exhibit irreversible defects in chromosome congression during mitosis, which induce a prolonged spindle assembly checkpoint-dependent mitotic arrest, followed by massive apoptosis, as revealed by live cell imaging. Collectively, the results indicate that the diarylpentanoid BP-M345 exerts its antiproliferative activity by inhibiting mitosis through microtubule perturbation and causing cancer cell death, thereby highlighting its potential as antitumor agent.
先前,我们报道了二芳基戊烷类化合物 BP-M345 对人类癌细胞的体外生长抑制作用。然而,当时,BP-M345 发挥其生长抑制作用的细胞机制仍有待探索。在本工作中,我们报告了其对癌细胞的作用机制。该化合物表现出很强的肿瘤生长抑制活性,且选择性指数高。从机制上讲,它通过微管不稳定诱导纺锤体的扰动。结果,经处理的细胞在有丝分裂过程中表现出染色体向心性的不可逆转缺陷,这会导致纺锤体组装检查点依赖性的有丝分裂停滞延长,随后大量细胞凋亡,这通过活细胞成像得到证实。总之,结果表明二芳基戊烷类化合物 BP-M345 通过微管扰动抑制有丝分裂来发挥其抗增殖活性,并导致癌细胞死亡,从而突出了其作为抗肿瘤药物的潜力。