Juli Giada, Oliverio Manuela, Bellizzi Dina, Gallo Cantafio Maria Eugenia, Grillone Katia, Passarino Giuseppe, Colica Carmela, Nardi Monica, Rossi Marco, Procopio Antonio, Tagliaferri Pierosandro, Tassone Pierfrancesco, Amodio Nicola
Department of Experimental and Clinical Medicine, Magna Graecia University of Catanzaro, 88100 Catanzaro, Italy.
Department of Health Science, Magna Graecia University of Catanzaro, 88100 Catanzaro, Italy.
Cancers (Basel). 2019 Jul 16;11(7):990. doi: 10.3390/cancers11070990.
Olive oil contains different biologically active polyphenols, among which oleacein, the most abundant secoiridoid, has recently emerged for its beneficial properties in various disease contexts. By using in vitro models of human multiple myeloma (MM), we here investigated the anti-tumor potential of oleacein and the underlying bio-molecular sequelae. Within a low micromolar range, oleacein reduced the viability of MM primary samples and cell lines even in the presence of bone marrow stromal cells (BMSCs), while sparing healthy peripheral blood mononuclear cells. We also demonstrated that oleacein inhibited MM cell clonogenicity, prompted cell cycle blockade and triggered apoptosis. We evaluated the epigenetic impact of oleacein on MM cells, and observed dose-dependent accumulation of both acetylated histones and α-tubulin, along with down-regulation of several class I/II histone deacetylases (HDACs) both at the mRNA and protein level, providing evidence of the HDAC inhibitory activity of this compound; conversely, no effect on global DNA methylation was found. Mechanistically, HDACs inhibition by oleacein was associated with down-regulation of Sp1, the major transactivator of HDACs promoter, Caspase 8 activation. Of potential translational significance, oleacein synergistically enhanced the in vitro anti-MM activity of the proteasome inhibitor carfilzomib. Altogether, these results indicate that oleacein is endowed with HDAC inhibitory properties, which associate with significant anti-MM activity both as single agent or in combination with carfilzomib. These findings may pave the way to novel potential anti-MM epi-therapeutic approaches based on natural agents.
橄榄油含有不同的生物活性多酚,其中最丰富的裂环烯醚萜橄榄苦素,最近因其在各种疾病背景下的有益特性而受到关注。通过使用人类多发性骨髓瘤(MM)的体外模型,我们在此研究了橄榄苦素的抗肿瘤潜力及其潜在的生物分子后遗症。在低微摩尔范围内,即使存在骨髓基质细胞(BMSC),橄榄苦素也能降低MM原代样本和细胞系的活力,同时不影响健康的外周血单核细胞。我们还证明,橄榄苦素抑制MM细胞的克隆形成能力,促使细胞周期阻滞并引发凋亡。我们评估了橄榄苦素对MM细胞的表观遗传影响,观察到乙酰化组蛋白和α-微管蛋白的剂量依赖性积累,以及几种I/II类组蛋白去乙酰化酶(HDAC)在mRNA和蛋白质水平的下调,这为该化合物的HDAC抑制活性提供了证据;相反,未发现对整体DNA甲基化有影响。从机制上讲,橄榄苦素对HDAC的抑制与HDAC启动子的主要反式激活因子Sp1的下调、半胱天冬酶8的激活有关。具有潜在转化意义的是,橄榄苦素协同增强了蛋白酶体抑制剂卡非佐米的体外抗MM活性。总之,这些结果表明橄榄苦素具有HDAC抑制特性,无论是作为单一药物还是与卡非佐米联合使用,都具有显著的抗MM活性。这些发现可能为基于天然药物的新型潜在抗MM表观治疗方法铺平道路。