Kai Masaya, Kanaya Noriko, Wu Shang V, Mendez Carlos, Nguyen Duc, Luu Thehang, Chen Shiuan
Department of Cancer Biology, Beckman Research Institute of the City of Hope, 1500 East Duarte Road, Duarte, CA, 91010, USA.
Breast Cancer Res Treat. 2015 Jun;151(2):281-94. doi: 10.1007/s10549-015-3376-5. Epub 2015 Apr 23.
The aim of this study is to investigate the efficacy of combining a histone deacetylase inhibitor (LBH589) and a breast cancer stem cells (BCSC)-targeting agent (salinomycin) as a novel combination therapy for triple-negative breast cancer (TNBC). We performed in vitro studies using the TNBC cell lines to examine the combined effect. We used the mammosphere and ALDEFLUOR assays to estimate BCSC self-renewal capacity and distribution of BCSCs, respectively. Synergistic analysis was performed using CalcuSyn software. For in vivo studies, aldehyde dehydrogenase 1 ALDH1-positive cells were injected into non-obese diabetic/severe combined immunodeficiency gamma (NSG) mice. After tumor formation, mice were treated with LBH589, salinomycin, or in combination. In a second mouse model, HCC1937 cells were first treated with each treatment and then injected into NSG mice. For mechanistic analysis, immunohistochemistry and Western blot analysis were performed using cell and tumor samples. HCC1937 cells displayed BCSC properties including self-renewal capacity, an ALDH1-positive cell population, and the ability to form tumors. Treatment of HCC1937 cells with LBH589 and salinomycin had a potent synergistic effect inhibiting TNBC cell proliferation, ALDH1-positive cells, and mammosphere growth. In xenograft mouse models treated with LBH589 and salinomycin, the drug combination effectively and synergistically inhibited tumor growth of ALDH1-positive cells. The drug combination exerted its effects by inducing apoptosis, arresting the cell cycle, and regulating epithelial-mesenchymal transition (EMT). Combination of LBH589 and salinomycin has a synergistic inhibitory effect on TNBC BCSCs by inducing apoptosis, arresting the cell cycle, and regulating EMT; with no apparent associated severe toxicity. This drug combination could therefore offer a new targeted therapeutic strategy for TNBC and warrants further clinical study in patients with TNBC.
本研究的目的是探讨将组蛋白去乙酰化酶抑制剂(LBH589)和一种靶向乳腺癌干细胞(BCSC)的药物(沙林霉素)联合使用作为三阴性乳腺癌(TNBC)新型联合治疗方案的疗效。我们使用TNBC细胞系进行了体外研究,以检验联合用药的效果。我们分别使用乳腺球和ALDEFLUOR检测法来评估BCSC的自我更新能力和BCSC的分布情况。使用CalcuSyn软件进行协同分析。对于体内研究,将醛脱氢酶1(ALDH1)阳性细胞注射到非肥胖糖尿病/严重联合免疫缺陷γ(NSG)小鼠体内。肿瘤形成后,用LBH589、沙林霉素或联合用药对小鼠进行治疗。在第二个小鼠模型中,首先用每种治疗方法处理HCC1937细胞,然后将其注射到NSG小鼠体内。为了进行机制分析,使用细胞和肿瘤样本进行免疫组织化学和蛋白质印迹分析。HCC1937细胞表现出BCSC特性,包括自我更新能力、ALDH1阳性细胞群体以及形成肿瘤的能力。用LBH589和沙林霉素处理HCC1937细胞具有强大的协同作用,可抑制TNBC细胞增殖、ALDH1阳性细胞以及乳腺球生长。在用LBH589和沙林霉素处理的异种移植小鼠模型中,联合用药有效且协同抑制了ALDH1阳性细胞的肿瘤生长。联合用药通过诱导细胞凋亡、使细胞周期停滞以及调节上皮-间质转化(EMT)发挥作用。LBH589和沙林霉素联合使用对TNBC BCSC具有协同抑制作用,可诱导细胞凋亡、使细胞周期停滞并调节EMT;且无明显相关严重毒性。因此,这种联合用药可为TNBC提供一种新的靶向治疗策略,值得对TNBC患者进行进一步的临床研究。