Department of Immunology and Regenerative Biology, Weizmann Institute of Science, Rehovot, Israel.
Department of Veterinary Resources, Weizmann Institute of Science, Rehovot, Israel.
Elife. 2024 Aug 2;13:RP96257. doi: 10.7554/eLife.96257.
Diffuse midline gliomas (DMGs) are aggressive and fatal pediatric tumors of the central nervous system that are highly resistant to treatments. Lysine to methionine substitution of residue 27 on histone H3 (H3-K27M) is a driver mutation in DMGs, reshaping the epigenetic landscape of these cells to promote tumorigenesis. H3-K27M gliomas are characterized by deregulation of histone acetylation and methylation pathways, as well as the oncogenic MYC pathway. In search of effective treatment, we examined the therapeutic potential of dual targeting of histone deacetylases (HDACs) and MYC in these tumors. Treatment of H3-K27M patient-derived cells with Sulfopin, an inhibitor shown to block MYC-driven tumors in vivo, in combination with the HDAC inhibitor Vorinostat, resulted in substantial decrease in cell viability. Moreover, transcriptome and epigenome profiling revealed synergistic effect of this drug combination in downregulation of prominent oncogenic pathways such as mTOR. Finally, in vivo studies of patient-derived orthotopic xenograft models showed significant tumor growth reduction in mice treated with the drug combination. These results highlight the combined treatment with PIN1 and HDAC inhibitors as a promising therapeutic approach for these aggressive tumors.
弥漫性中线胶质瘤(DMG)是一种侵袭性和致命性的儿童中枢神经系统肿瘤,对治疗具有高度抗性。组蛋白 H3 赖氨酸 27 到蛋氨酸的取代(H3-K27M)是 DMG 的驱动突变,重塑了这些细胞的表观遗传景观,促进了肿瘤的发生。H3-K27M 神经胶质瘤的特征是组蛋白乙酰化和甲基化途径以及致癌 MYC 途径的失调。为了寻找有效的治疗方法,我们研究了双重靶向组蛋白去乙酰化酶(HDACs)和 MYC 在这些肿瘤中的治疗潜力。用 Sulfopin(一种已被证明可在体内阻断 MYC 驱动的肿瘤的抑制剂)联合 HDAC 抑制剂 Vorinostat 治疗 H3-K27M 患者来源的细胞,可显著降低细胞活力。此外,转录组和表观基因组分析显示,这种药物组合在下调突出的致癌途径(如 mTOR)方面具有协同作用。最后,在患者来源的原位异种移植模型的体内研究中,用药物组合治疗的小鼠肿瘤生长显著减少。这些结果突出了 PIN1 和 HDAC 抑制剂联合治疗作为这些侵袭性肿瘤的一种有前途的治疗方法。