Departamento de Biología Molecular y Biotecnología, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, Ciudad de México 04510, Mexico.
Departamento de Biología de la Reproducción Dr. Carlos Gual Castro, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Vasco de Quiroga No. 15, Belisario Domínguez Sección XVI, Tlalpan, Ciudad de México 14080, Mexico.
Int J Mol Sci. 2024 Mar 9;25(6):3165. doi: 10.3390/ijms25063165.
HER2-positive breast cancer is associated with aggressive behavior and reduced survival rates. Calcitriol restores the antiproliferative activity of antiestrogens in estrogen receptor (ER)-negative breast cancer cells by re-expressing ERα. Furthermore, calcitriol and its analog, EB1089, enhance responses to standard anti-cancer drugs. Therefore, we aimed to investigate EB1089 effects when added to the combined treatment of lapatinib and antiestrogens on the proliferation of HER2-positive breast cancer cells. BT-474 (ER-positive/HER2-positive) and SK-BR-3 (ER-negative/HER2-positive) cells were pre-treated with EB1089 to modulate ER expression. Then, cells were treated with EB1089 in the presence of lapatinib with or without the antiestrogens, and proliferation, phosphorylation array assays, and Western blot analysis were performed. The results showed that EB1089 restored the antiproliferative response to antiestrogens in SK-BR-3 cells and improved the inhibitory effects of the combination of lapatinib with antiestrogens in the two cell lines. Moreover, EB1089, alone or combined, modulated ERα protein expression and reduced Akt phosphorylation in HER2-positive cells. EB1089 significantly enhanced the cell growth inhibitory effect of lapatinib combined with antiestrogens in HER2-positive breast cancer cells by modulating ERα expression and Akt phosphorylation suppression. These results highlight the potential of this therapeutic approach as a promising strategy for managing HER2-positive breast cancer.
人表皮生长因子受体 2 阳性乳腺癌具有侵袭性且生存率降低。骨化三醇通过重新表达雌激素受体 α(ERα),恢复了抗雌激素在雌激素受体(ER)阴性乳腺癌细胞中的抗增殖活性。此外,骨化三醇及其类似物 EB1089 增强了对标准抗癌药物的反应。因此,我们旨在研究 EB1089 与拉帕替尼和抗雌激素联合治疗对人表皮生长因子受体 2 阳性乳腺癌细胞增殖的影响。BT-474(ER 阳性/HER2 阳性)和 SK-BR-3(ER 阴性/HER2 阳性)细胞用 EB1089 预处理以调节 ER 表达。然后,在存在或不存在抗雌激素的情况下,用 EB1089 处理细胞,并进行增殖、磷酸化阵列分析和 Western blot 分析。结果表明,EB1089 恢复了 SK-BR-3 细胞对抗雌激素的增殖反应,并改善了拉帕替尼与抗雌激素联合治疗在两种细胞系中的抑制作用。此外,EB1089 单独或联合使用均可调节 ERα 蛋白表达并降低 HER2 阳性细胞中的 Akt 磷酸化。EB1089 通过调节 ERα 表达和抑制 Akt 磷酸化,显著增强了拉帕替尼联合抗雌激素对 HER2 阳性乳腺癌细胞的生长抑制作用。这些结果突出了这种治疗方法的潜力,为管理 HER2 阳性乳腺癌提供了一种有前途的策略。