The Research Progress of Metformin Regulation of Metabolic Reprogramming in Malignant Tumors.

IF 3.5 3区 医学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Qihai Sui, Huiqiang Yang, Zhengyang Hu, Xing Jin, Zhencong Chen, Wei Jiang, Fenghao Sun
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引用次数: 0

Abstract

Background: Metabolism reprogramming is a crucial hallmark of malignant tumors. Tumor cells demonstrate enhanced metabolic efficiency, converting nutrient inputs into glucose, amino acids, and lipids essential for their malignant proliferation and progression. Metformin, a commonly prescribed medication for type 2 diabetes mellitus, has garnered attention for its potential anticancer effects beyond its established hypoglycemic benefits.

Methods: This review adopts a comprehensive approach to delineate the mechanisms underlying metabolite abnormalities within the primary metabolic processes of malignant tumors.

Results: This review examines the abnormal activation of G protein-coupled receptors (GPCRs) in these metabolic pathways, encompassing aerobic glycolysis with increased lactate production in glucose metabolism, heightened lipid synthesis and cholesterol accumulation in lipid metabolism, and glutamine activation alongside abnormal protein post-translational modifications in amino acid and protein metabolism. Furthermore, the intricate metabolic pathways and molecular mechanisms through which metformin exerts its anticancer effects are synthesized and analyzed, particularly its impacts on AMP-activated protein kinase activation and the mTOR pathway. The analysis reveals a multifaceted understanding of how metformin can modulate tumor metabolism, targeting key nodes in metabolic reprogramming essential for tumor growth and progression. The review compiles evidence that supports metformin's potential as an adjuvant therapy for malignant tumors, highlighting its capacity to interfere with critical metabolic pathways.

Conclusion: In conclusion, this review offers a comprehensive overview of the plausible mechanisms mediating metformin's influence on tumor metabolism, fostering a deeper comprehension of its anticancer mechanisms. By expanding the clinical horizons of metformin and providing insight into metabolism-targeted tumor therapies, this review lays the groundwork for future research endeavors aimed at refining and advancing metabolic intervention strategies for cancer treatment.

二甲双胍调控恶性肿瘤代谢重编程的研究进展。
背景:代谢重编程是恶性肿瘤的一个重要特征。肿瘤细胞显示出更高的代谢效率,可将输入的营养物质转化为葡萄糖、氨基酸和脂质,这些物质对肿瘤的恶性增殖和发展至关重要。二甲双胍是治疗 2 型糖尿病的常用处方药,其潜在的抗癌作用已超出其既有的降血糖功效,因而备受关注:方法:本综述采用综合方法来描述恶性肿瘤主要代谢过程中代谢物异常的内在机制:本综述研究了这些代谢途径中 G 蛋白偶联受体 (GPCR) 的异常激活,包括葡萄糖代谢中乳酸生成增加的有氧糖酵解、脂质代谢中脂质合成增加和胆固醇积累,以及氨基酸和蛋白质代谢中谷氨酰胺激活和蛋白质翻译后修饰异常。此外,还综合分析了二甲双胍发挥抗癌作用的复杂代谢途径和分子机制,特别是其对 AMP 激活蛋白激酶活化和 mTOR 途径的影响。分析揭示了对二甲双胍如何调节肿瘤代谢的多方面理解,针对肿瘤生长和进展所必需的代谢重编程的关键节点。综述汇编了支持二甲双胍作为恶性肿瘤辅助疗法潜力的证据,强调了二甲双胍干扰关键代谢途径的能力:总之,这篇综述全面概述了二甲双胍影响肿瘤代谢的合理机制,有助于加深对其抗癌机制的理解。这篇综述拓展了二甲双胍的临床视野,为以代谢为靶点的肿瘤疗法提供了见解,为今后旨在完善和推进癌症治疗代谢干预策略的研究工作奠定了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Pharmaceutical Research
Pharmaceutical Research 医学-化学综合
CiteScore
6.60
自引率
5.40%
发文量
276
审稿时长
3.4 months
期刊介绍: Pharmaceutical Research, an official journal of the American Association of Pharmaceutical Scientists, is committed to publishing novel research that is mechanism-based, hypothesis-driven and addresses significant issues in drug discovery, development and regulation. Current areas of interest include, but are not limited to: -(pre)formulation engineering and processing- computational biopharmaceutics- drug delivery and targeting- molecular biopharmaceutics and drug disposition (including cellular and molecular pharmacology)- pharmacokinetics, pharmacodynamics and pharmacogenetics. Research may involve nonclinical and clinical studies, and utilize both in vitro and in vivo approaches. Studies on small drug molecules, pharmaceutical solid materials (including biomaterials, polymers and nanoparticles) biotechnology products (including genes, peptides, proteins and vaccines), and genetically engineered cells are welcome.
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