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Journal ArticleDOI

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

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TLDR
The interesting properties of metformin such as radioprotection, radiomitigation and radiosensitization could make it an interesting adjuvant for clinical radiotherapy, as well as an interesting candidate for mitigation of radiation injury after a radiation disaster.
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. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.

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Journal ArticleDOI

Steps in metastasis: an updated review.

TL;DR: In this article, the tumor cells isolated from the primary tumor exploit several mechanisms to maintain their survival including rewiring metabolic demands to use sources available within the new environments, avoiding anoikis cell death when cells are detached from extracellular matrix (ECM), adopting flow mechanic by acquiring platelet shielding and immunosuppression by negating the activity of suppressor immune cells, such as natural killer (NK) cells.
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Radioprotection and Radiomitigation: From the Bench to Clinical Practice.

TL;DR: Molecules under development with the aim of reaching clinical practice and other nonclinical applications are discussed and differentiates radioprotectors and radiomitigators (minimize toxicity even after radiation has been delivered).
Journal ArticleDOI

Targeting of oxidative stress and inflammation through ROS/NF-kappaB pathway in phosphine-induced hepatotoxicity mitigation

TL;DR: Targeting ROS/NF-kappaB signalling pathway by resveratrol may have a significant effect on the improvement of hepatic injury induced by phosphine, suggesting it may be a possible candidate for the treatment of phosphine-poisoning.
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Metformin: The Answer to Cancer in a Flower? Current Knowledge and Future Prospects of Metformin as an Anti-Cancer Agent in Breast Cancer

TL;DR: The biology of metformin and its molecular mechanism of action is discussed, the existing cellular, pre-clinical, and clinical studies that have tested the anti-tumor potential of meetformin as a potential anti-cancer/anti-Tumor agent in breast cancer therapy are discussed, and the future prospects and directions for a better understanding and re-purposing of met formin as an anti- cancer drug in the treatment of breast cancer are outlined.
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Enriched cancer stem cells, dense stroma, and cold immunity: Interrelated events in pancreatic cancer.

TL;DR: In this article, the authors investigated how desmoplastic aggregates can influence the functionality of CSCs for promoting a cold pancreatic tumor immunity, which can be an effective strategy for improving responses from cold tumors to immunotherapy.
References
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Journal ArticleDOI

Metformin use improves survival of diabetic liver cancer patients: systematic review and meta-analysis.

TL;DR: The results indicated that metformin use improved survival of diabetic liver cancer patients, however, the results should be interpreted with caution given the possibility of residual confounding.
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Contributions of AMPK and p53 dependent signaling to radiation response in the presence of metformin

TL;DR: The anti-proliferative activity of metformin may confer benefit in combination with radiotherapy, and this benefit is intensified upon loss of AMPK or p53 signaling.
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Metformin suppresses tumor angiogenesis and enhances the chemosensitivity of gemcitabine in a genetically engineered mouse model of pancreatic cancer.

TL;DR: It is concluded that metformin suppressed tumor angiogenesis and enhanced the chemosensitivity of gemcitabine via inactivating PSCs in PDAC of KPC mice.
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Role of p53, Bax, p21, and DNA-PKcs in radiation sensitivity of HCT-116 cells and xenografts.

TL;DR: The contribution of p53, p21, Bax, and DNA-PKcs in response to ionizing radiation in an isogeneic colorectal cancer system in vitro and in vivo is investigated.
Journal ArticleDOI

Molecular hydrogen and radiation protection

TL;DR: The protective effect of H2 in irradiated cells and mice for the first time is reported, and encouraging results suggested that H2 has a potential as a radioprotective agent with efficacy and non-toxicity.
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