van Dyk Lorinda, Verhoog Nicolette J D, Louw Ann
Department of Biochemistry, Stellenbosch University, Stellenbosch, South Africa.
Front Pharmacol. 2022 Sep 22;13:1017690. doi: 10.3389/fphar.2022.1017690. eCollection 2022.
Synergistic drug combinations are not only popular in antibiotic, anti-microbial, immune disease (i.e., AIDS) and viral infection studies, but has also gained traction in the field of cancer research as a multi-targeted approach. It has the potential to lower the doses needed of standard of care (SOC) therapeutic agents, whilst maintaining an effective therapeutic level. Lower dosages could ameliorate the fundamental problems such as drug resistance and metastasis associated with current SOC therapies. In the current study, we show that the combination of SM6Met with (2)-4-hydroxytamoxifen (4-OH-Tam, the active metabolite of tamoxifen) produces a strong synergistic effect in terms of inhibiting MCF7 ER-positive (ER) breast cancer cell proliferation and that a 20 times lower dose of 4-OH-Tam in combination with SM6Met is required to produce the same inhibitory effect on cell proliferation as 4-OH-Tam on its own. Cell cycle analyses of the best combination ratios of SM6Met and 4-OH-Tam also suggests that the combination results in increased accumulation of cells in the S-phase and in the apoptotic phase. Moreover, the best combination ratio (20:1) of SM6Met with 4-OH-Tam displayed greater anti-metastatic potential in terms of inhibiting ER breast cancer cell migration, invasion, and colony formation than the SOC therapy alone, suggesting that SM6Met together with 4-OH-Tam could be a viable drug combination for not only delaying resistance and ameliorating the negative side-effects associated with current SOC therapies, like tamoxifen, but could also provide a novel, more affordable therapeutic alternative for treating or preventing ER breast cancer metastasis.
协同药物组合不仅在抗生素、抗微生物、免疫疾病(如艾滋病)和病毒感染研究中很常见,而且作为一种多靶点方法在癌症研究领域也越来越受到关注。它有可能降低标准治疗(SOC)治疗药物所需的剂量,同时保持有效的治疗水平。较低的剂量可以改善与当前SOC疗法相关的耐药性和转移等基本问题。在本研究中,我们表明SM6Met与(2)-4-羟基他莫昔芬(4-OH-Tam,他莫昔芬的活性代谢物)联合使用在抑制MCF7雌激素受体阳性(ER)乳腺癌细胞增殖方面产生了强烈的协同效应,并且与单独使用4-OH-Tam相比,联合使用低20倍剂量的4-OH-Tam与SM6Met就能产生相同的细胞增殖抑制效果。对SM6Met和4-OH-Tam最佳组合比例进行的细胞周期分析还表明,该组合导致细胞在S期和凋亡期的积累增加。此外,SM6Met与4-OH-Tam的最佳组合比例(20:1)在抑制ER乳腺癌细胞迁移、侵袭和集落形成方面显示出比单独的SOC疗法更大的抗转移潜力,这表明SM6Met与4-OH-Tam联合使用不仅可以延缓耐药性并改善与当前SOC疗法(如他莫昔芬)相关的负面副作用,还可以为治疗或预防ER乳腺癌转移提供一种新的、更经济实惠的治疗选择。