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Synergistic effects of combined treatment with histone deacetylase inhibitor suberoylanilide hydroxamic acid and TRAIL on human breast cancer cells

机译:组蛋白脱乙酰基酶抑制剂亚磺酰苯胺异羟肟酸和TRAIL联合治疗对人乳腺癌细胞的协同作用

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摘要

Previous studies showed that either histone deacetylase (HDAC) inhibitors or tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) can induce apoptosis in tumor cells including breast cancer. However, the underling mechanisms of combining HDAC inhibitors with TRAIL in the treatment of breast cancer are poorly understood. In this study, we determined the ability of SAHA and TRAIL as single agents or in combination to inhibit the growth and survival of MCF-7 and MDA-MB-231 breast cancer cells. Our results demonstrate that the distinct effects of SAHA or TRAIL individually and in combination on the proliferation, cell viability, apoptosis, cell cycle distribution, and morphological changes of MDA-MB-231 and MCF-7 cells. We further determined the different effects of SAHA or TRAIL alone and combining SAHA with TRAIL on the expression of a number of apoptosis-related molecules, cell cycle, growth factors and their receptors in cancer cells. Our results demonstrated that the combinatorial treatment of SAHA and TRAIL may target multiple pathways and serve as an effective therapeutic strategy against breast cancer. An improved understanding of the molecular mechanisms may facilitate either SAHA or TRAIL targeted use and the selection of suitable combinations.
机译:先前的研究表明,组蛋白脱乙酰基酶(HDAC)抑制剂或肿瘤坏死因子相关的凋亡诱导配体(TRAIL)均可诱导包括乳腺癌在内的肿瘤细胞凋亡。然而,人们对将HDAC抑制剂与TRAIL联合治疗乳腺癌的基本机制了解甚少。在这项研究中,我们确定了SAHA和TRAIL作为单一药物或组合药物抑制MCF-7和MDA-MB-231乳腺癌细胞生长和存活的能力。我们的结果表明,单独或联合使用SAHA或TRAIL对MDA-MB-231和MCF-7细胞的增殖,细胞活力,凋亡,细胞周期分布和形态变化具有明显的影响。我们进一步确定了单独使用SAHA或TRAIL以及将SAHA与TRAIL结合对癌细胞中许多凋亡相关分子,细胞周期,生长因子及其受体的表达的不同影响。我们的结果表明,SAHA和TRAIL的联合治疗可能靶向多种途径,并成为抗乳腺癌的有效治疗策略。更好地理解分子机制可以促进SAHA或TRAIL的靶向使用以及合适组合的选择。

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