Metformin as a Radiation Modifier; Implications to Normal Tissue Protection and Tumor Sensitization.

IF 3.2 Q2 Pharmacology, Toxicology and Pharmaceutics
Keywan Mortezaee, Dheyauldeen Shabeeb, Ahmed E Musa, Masoud Najafi, Bagher Farhood
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引用次数: 58

Abstract

Background: Nowadays, ionizing radiation is used for several applications in medicine, industry, agriculture, and nuclear power generation. Besides the beneficial roles of ionizing radiation, there are some concerns about accidental exposure to radioactive sources. The threat posed by its use in terrorism is of global concern. Furthermore, there are several side effects to normal organs for patients who had undergone radiation treatment for cancer. Hence, the modulation of radiation response in normal tissues was one of the most important aims of radiobiology. Although, so far, several agents have been investigated for protection and mitigation of radiation injury. Agents such as amifostine may lead to severe toxicity, while others may interfere with radiation therapy outcomes as a result of tumor protection. Metformin is a natural agent that is well known as an antidiabetic drug. It has shown some antioxidant effects and enhances DNA repair capacity, thereby ameliorating cell death following exposure to radiation. Moreover, through targeting endogenous ROS production within cells, it can mitigate radiation injury. This could potentially make it an effective radiation countermeasure. In contrast to other radioprotectors, metformin has shown modulatory effects through induction of several genes such as AMPK, which suppresses reduction/ oxidation (redox) reactions, protects cells from accumulation of unrepaired DNA, and attenuates initiation of inflammation as well as fibrotic pathways. Interestingly, these properties of metformin can sensitize cancer cells to radiotherapy.

Conclusion: In this article, we aimed to review the interesting properties of metformin such as radioprotection, radiomitigation and radiosensitization, which could make it an interesting adjuvant for clinical radiotherapy, as well as an interesting candidate for mitigation of radiation injury after a radiation disaster.

二甲双胍作为辐射调节剂的研究正常组织保护和肿瘤致敏的意义。
背景:目前,电离辐射在医药、工业、农业和核能发电等领域有着广泛的应用。除了电离辐射的有益作用外,还有一些关于意外暴露于放射源的担忧。将其用于恐怖主义所构成的威胁是全球关注的问题。此外,接受放射治疗的癌症患者的正常器官也有一些副作用。因此,正常组织中辐射反应的调节是放射生物学最重要的目标之一。尽管到目前为止,已经研究了几种剂来保护和减轻辐射损伤。氨磷汀等药物可能导致严重的毒性,而其他药物可能由于肿瘤保护而干扰放射治疗的结果。二甲双胍是一种天然的抗糖尿病药物。它显示出一些抗氧化作用,增强DNA修复能力,从而改善暴露于辐射后的细胞死亡。此外,通过靶向细胞内内源性ROS的产生,它可以减轻辐射损伤。这可能使它成为一种有效的辐射对抗手段。与其他放射保护剂相比,二甲双胍通过诱导几种基因(如AMPK)显示出调节作用,AMPK可以抑制还原/氧化(氧化还原)反应,保护细胞免受未修复DNA的积累,并减弱炎症和纤维化途径的启动。有趣的是,二甲双胍的这些特性可以使癌细胞对放射治疗敏感。结论:本文旨在综述二甲双胍在放射防护、放射缓解和放射致敏等方面的有趣特性,使其成为临床放疗的有趣佐剂,以及放射灾害后减轻辐射损伤的有趣候选者。
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
Current clinical pharmacology
Current clinical pharmacology PHARMACOLOGY & PHARMACY-
CiteScore
3.60
自引率
0.00%
发文量
0
期刊介绍: Current Clinical Pharmacology publishes frontier reviews on all the latest advances in clinical pharmacology. The journal"s aim is to publish the highest quality review articles in the field. Topics covered include: pharmacokinetics; therapeutic trials; adverse drug reactions; drug interactions; drug metabolism; pharmacoepidemiology; and drug development. The journal is essential reading for all researchers in clinical pharmacology.
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