替莫唑胺、二甲双胍和表没食子儿茶素没食子酸酯在胶质母细胞瘤中的协同抗沃伯格效应

IF 3.3 3区 医学 Q2 PHARMACOLOGY & PHARMACY Toxicology and applied pharmacology Pub Date : 2024-11-06 DOI:10.1016/j.taap.2024.117146
Shreyas S. Kuduvalli , Daisy Precilla Senthilathiban , Indrani Biswas , Justin S. Antony , Madhu Subramani , T.S. Anitha
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引用次数: 0

摘要

胶质母细胞瘤侵袭性的一个重要特征是其葡萄糖代谢的改变。通过线粒体氧化磷酸化的重编程,肿瘤细胞无论氧气供应情况如何都会进行有氧糖酵解,这种代谢转变被称为沃伯格效应。以前的文献已将这种代谢重编程与肿瘤进展和胶质母细胞瘤细胞增殖联系起来,使其成为靶向药物治疗的关键目标。基于这一空白,本研究旨在探讨替莫唑胺、二甲双胍和表没食子儿茶素没食子酸酯三药联合疗法在体外和体内减轻胶质母细胞瘤的沃伯格效应和葡萄糖摄取的疗效。我们的研究结果表明,三药联合使用可显著降低胶质母细胞瘤细胞和胶质瘤诱导的异种移植大鼠模型的葡萄糖摄取,并逆转沃伯格效应。因此,三药联合可作为一种有效的治疗方案,通过改变葡萄糖代谢来阻碍胶质母细胞瘤的发展,并改善患者的整体预后。
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The synergistic anti-Warburg efficacy of temozolomide, metformin and epigallocatechin gallate in glioblastoma
An important hallmark of glioblastoma aggressiveness is its altered metabolism of glucose. This metabolic shift wherein the tumor cells employ aerobic glycolysis regardless of oxygen availability via reprogramming of mitochondrial oxidative phosphorylation is known as the Warburg effect. Previous literatures have linked this metabolic reprograming to tumor progression and glioblastoma cell proliferation making it a key target for targeted drug therapy. Based on this lacuna, the current study aimed to explore the therapeutic efficacy of the triple-drug combination of temozolomide, metformin and epigallocatechin gallate in attenuating Warburg effect and glucose uptake in glioblastoma both in vitro and in vivo. Our results showed that the triple-drug combination had significantly reduced glucose uptake and reversed the Warburg effect in glioblastoma cells and in the glioma-induced xenograft rat model. Thus, the triple-drug combination would serve as an effective therapeutic regime to hamper glioblastoma progression via altering glucose metabolism and improving the overall prognosis in patient setting.
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来源期刊
CiteScore
6.80
自引率
2.60%
发文量
309
审稿时长
32 days
期刊介绍: Toxicology and Applied Pharmacology publishes original scientific research of relevance to animals or humans pertaining to the action of chemicals, drugs, or chemically-defined natural products. Regular articles address mechanistic approaches to physiological, pharmacologic, biochemical, cellular, or molecular understanding of toxicologic/pathologic lesions and to methods used to describe these responses. Safety Science articles address outstanding state-of-the-art preclinical and human translational characterization of drug and chemical safety employing cutting-edge science. Highly significant Regulatory Safety Science articles will also be considered in this category. Papers concerned with alternatives to the use of experimental animals are encouraged. Short articles report on high impact studies of broad interest to readers of TAAP that would benefit from rapid publication. These articles should contain no more than a combined total of four figures and tables. Authors should include in their cover letter the justification for consideration of their manuscript as a short article.
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