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首页> 外文期刊>Journal of neuro-oncology. >Synergistic induction of NY-ESO-1 antigen expression by a novel histone deacetylase inhibitor, valproic acid, with 5-aza-2'-deoxycytidine in glioma cells.
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Synergistic induction of NY-ESO-1 antigen expression by a novel histone deacetylase inhibitor, valproic acid, with 5-aza-2'-deoxycytidine in glioma cells.

机译:新型组蛋白脱乙酰基酶抑制剂丙戊酸与5-氮杂-2'-脱氧胞苷在神经胶质瘤细胞中协同诱导NY-ESO-1抗原表达。

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摘要

NY-ESO-1, one of the most immunogenic cancer/testis antigens, provides attractive targets for cancer immunotherapy. NY-ESO-1 has been demonstrated to be expressed in a range of solid tumors via DNA demethylation and/or histone modification; however, it has been rarely expressed in glioma. The reversibility of these epigenetic aberrations is potentially attractive for glioma treatment with DNA-methyltransferase inhibitors (DNMTi) and histone deacetylase inhibitors (HDACi), leading to reactivation of silenced genes. We previously demonstrated de novo induction of NY-ESO-1 in glioma cells by DNMTi. In this study, we show that an anticonvulsant, i.e., valproic acid (VPA), also acting as an HDACi, enhances induction of NY-ESO-1 in synergy with DNMTi. Chromatin assays demonstrated that combination of DNMTi and VPA elicited significant DNA demethylation, histone H3 Lys9 demethylation, and acetylation. These findings not only shed light on an epigenetic immunotherapy, but also suggest that the silencing of NY-ESO-1 is mediated by histone modification.
机译:NY-ESO-1是最具免疫原性的癌症/睾丸抗原之一,为癌症免疫治疗提供了有吸引力的靶标。已证明NY-ESO-1可通过DNA脱甲基和/或组蛋白修饰在一系列实体瘤中表达;但是,它在神经胶质瘤中很少表达。这些表观遗传畸变的可逆性对于用DNA-甲基转移酶抑制剂(DNMTi)和组蛋白脱乙酰基酶抑制剂(HDACi)治疗神经胶质瘤可能具有吸引力,从而导致沉默基因的重新激活。我们以前证明了DNMTi在神经胶质瘤细胞中从头诱导NY-ESO-1。在这项研究中,我们表明抗惊厥药,即丙戊酸(VPA),也可作为HDACi,与DNMTi协同增强NY-ESO-1的诱导。染色质分析表明,DNMTi和VPA的结合可引起明显的DNA脱甲基,组蛋白H3 Lys9脱甲基和乙酰化。这些发现不仅阐明了表观遗传学免疫疗法,而且表明,NY-ESO-1的沉默是由组蛋白修饰介导的。

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