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Targeting metabolic/epigenetic pathways: a potential strategy for cancer therapy in diffuse intrinsic pontine gliomas

机译:靶向代谢/表观遗传途径:弥漫性内在卵巢肿瘤性癌症患者癌症治疗的潜在策略

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A recent study published in Cancer Cell by Chan Chung andcolleagues demonstrated that H3.3K27M mutation in diffuseintrinsic pontine gliomas (DIPGs) potentiated glycolysis, tricarboxylicacid cycle, and glutaminolysis metabolism with upregulatedalpha-ketoglutarate (α-KG), which contributed to sustain anepigenetic status marked by H3K27me3 deficiency and thatinterruption of these metabolic/epigenetic pathways representeda promising strategy for the treatment of DIPGs, as reprted byChung, C. et al.
机译:Chan Chung和Colleagues在癌细胞中发表的最近的一项研究表明,衍射杂体猪的衍生物(DIPGS)的H3.3k27m突变有助于upregulatedalpha-ketoglutarate(α-kg),这有助于维持标记的吞咽血管状态通过H3K27ME3的缺陷和这些代谢/表观遗传途径的缺乏和该代购探讨的探讨是对DIPGS的治疗,如被Chung,C.等人的再生。

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