Hajimohammadebrahim-Ketabforoush Melika, Zali Alireza, Shahmohammadi Mohammadreza, Hamidieh Amir Ali
Student Research Committee, Department of Clinical Nutrition and Dietetics, Faculty of Nutrition Sciences and Food Technology, National Nutrition and Food Technology Research Institute, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Functional Neurosurgery Research Center, Shohada Tajrish Comprehensive Neurosurgical Center of Excellence, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Front Oncol. 2024 Aug 29;14:1455492. doi: 10.3389/fonc.2024.1455492. eCollection 2024.
Despite reaching enormous achievements in therapeutic approaches worldwide, GBM still remains the most incurable malignancy among various cancers. It emphasizes the necessity of adjuvant therapies from the perspectives of both patients and healthcare providers. Therefore, most emerging studies have focused on various complementary and adjuvant therapies. Among them, metabolic therapy has received special attention, and metformin has been considered as a treatment in various types of cancer, including GBM. It is clearly evident that reaching efficient approaches without a comprehensive evaluation of the key mechanisms is not possible. Among the studied mechanisms, one of the more challenging ones is the effect of metformin on apoptosis and senescence. Moreover, metformin is well known as an insulin sensitizer. However, if insulin signaling is facilitated in the tumor microenvironment, it may result in tumor growth. Therefore, to partially resolve some paradoxical issues, we conducted a narrative review of related studies to address the following questions as comprehensively as possible: 1) Does the improvement of cellular insulin function resulting from metformin have detrimental or beneficial effects on GBM cells? 2) If these effects are detrimental to GBM cells, which is more important: apoptosis or senescence? 3) What determines the cellular decision between apoptosis and senescence?
尽管全球范围内在治疗方法上取得了巨大成就,但胶质母细胞瘤(GBM)在各种癌症中仍然是最难治愈的恶性肿瘤。这从患者和医疗服务提供者的角度都凸显了辅助治疗的必要性。因此,大多数新兴研究都集中在各种补充和辅助治疗上。其中,代谢疗法受到了特别关注,二甲双胍已被视为包括GBM在内的各种癌症的一种治疗方法。显然,如果不全面评估关键机制,就不可能找到有效的方法。在已研究的机制中,更具挑战性的机制之一是二甲双胍对细胞凋亡和衰老的影响。此外,二甲双胍是众所周知的胰岛素增敏剂。然而,如果在肿瘤微环境中促进胰岛素信号传导,可能会导致肿瘤生长。因此,为了部分解决一些矛盾问题,我们对相关研究进行了叙述性综述,以尽可能全面地回答以下问题:1)二甲双胍导致的细胞胰岛素功能改善对GBM细胞有有害还是有益的影响?2)如果这些影响对GBM细胞有害,哪个更重要:细胞凋亡还是衰老?3)是什么决定了细胞在凋亡和衰老之间的抉择?