首页> 美国卫生研究院文献>Journal of Hematology Oncology >The first-in-class alkylating deacetylase inhibitor molecule tinostamustine shows antitumor effects and is synergistic with radiotherapy in preclinical models of glioblastoma
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The first-in-class alkylating deacetylase inhibitor molecule tinostamustine shows antitumor effects and is synergistic with radiotherapy in preclinical models of glioblastoma

机译:一流的烷基化脱乙酰基酶抑制剂分子锡莫司汀在成胶质母细胞瘤的临床前模型中显示抗肿瘤作用并与放疗协同作用

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摘要

BackgroundThe use of alkylating agents such as temozolomide in association with radiotherapy (RT) is the therapeutic standard of glioblastoma (GBM). This regimen modestly prolongs overall survival, also if, in light of the still dismal prognosis, further improvements are desperately needed, especially in the patients with O6-methylguanine-DNA-methyltransferase (MGMT) unmethylated tumors, in which the benefit of standard treatment is less. Tinostamustine (EDO-S101) is a first-in-class alkylating deacetylase inhibitor (AK-DACi) molecule that fuses the DNA damaging effect of bendamustine with the fully functional pan-histone deacetylase (HDAC) inhibitor, vorinostat, in a completely new chemical entity.
机译:背景技术与放疗(RT)结合使用的替莫唑胺等烷基化剂是胶质母细胞瘤(GBM)的治疗标准。鉴于预后仍然很差,如果急需进一步改善,特别是在O6-甲基鸟嘌呤-DNA-甲基转移酶(MGMT)非甲基化肿瘤的患者中,该方案可适度延长总体生存期,其中标准治疗的益处是减。替诺莫司汀(EDO-S101)是一流的烷基化脱乙酰基酶抑制剂(AK-DACi)分子,它以全新的化学性质融合了苯达莫司汀与全功能泛组蛋白脱乙酰基酶(HDAC)抑制剂伏立诺他的DNA破坏作用。实体。

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