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抗癌药物研发进展:二甲双胍作为胶质母细胞瘤抗血管生成的辅助治疗。

Advances in Anti-Cancer Drug Development: Metformin as Anti-Angiogenic Supplemental Treatment for Glioblastoma.

机构信息

Department of Neurosurgery, University of Florida, Gainesville, FL 32608, USA.

College of Medicine at Chicago, University of Illinois, Chicago, IL 60612, USA.

出版信息

Int J Mol Sci. 2024 May 23;25(11):5694. doi: 10.3390/ijms25115694.

DOI:10.3390/ijms25115694
PMID:38891882
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11171521/
Abstract

According to the WHO 2016 classification, glioblastoma is the most prevalent primary tumor in the adult central nervous system (CNS) and is categorized as grade IV. With an average lifespan of about 15 months from diagnosis, glioblastoma has a poor prognosis and presents a significant treatment challenge. Aberrant angiogenesis, which promotes tumor neovascularization and is a prospective target for molecular target treatment, is one of its unique and aggressive characteristics. Recently, the existence of glioma stem cells (GSCs) within the tumor, which are tolerant to chemotherapy and radiation, has been linked to the highly aggressive form of glioblastoma. Anti-angiogenic medications have not significantly improved overall survival (OS), despite various preclinical investigations and clinical trials demonstrating encouraging results. This suggests the need to discover new treatment options. Glioblastoma is one of the numerous cancers for which metformin, an anti-hyperglycemic medication belonging to the Biguanides family, is used as first-line therapy for type 2 diabetes mellitus (T2DM), and it has shown both in vitro and in vivo anti-tumoral activity. Based on these findings, the medication has been repurposed, which has shown the inhibition of many oncopromoter mechanisms and, as a result, identified the molecular pathways involved. Metformin inhibits cancer cell growth by blocking the LKB1/AMPK/mTOR/S6K1 pathway, leading to selective cell death in GSCs and inhibiting the proliferation of CD133+ cells. It has minimal impact on differentiated glioblastoma cells and normal human stem cells. The systematic retrieval of information was performed on PubMed. A total of 106 articles were found in a search on metformin for glioblastoma. Out of these six articles were Meta-analyses, Randomized Controlled Trials, clinical trials, and Systematic Reviews. The rest were Literature review articles. These articles were from the years 2011 to 2024. Appropriate studies were isolated, and important information from each of them was understood and entered into a database from which the information was used in this article. The clinical trials on metformin use in the treatment of glioblastoma were searched on clinicaltrials.gov. In this article, we examine and evaluate metformin's possible anti-tumoral effects on glioblastoma, determining whether or not it may appropriately function as an anti-angiogenic substance and be safely added to the treatment and management of glioblastoma patients.

摘要

根据世界卫生组织 2016 年的分类,胶质母细胞瘤是成人中枢神经系统(CNS)中最常见的原发性肿瘤,归类为 4 级。从诊断到平均存活期约为 15 个月,胶质母细胞瘤预后不良,治疗极具挑战性。异常血管生成促进肿瘤新生血管形成,是分子靶向治疗的潜在靶点,是其独特而具有侵袭性的特征之一。最近,肿瘤内存在对化疗和放疗具有耐受性的胶质瘤干细胞(GSCs)与胶质母细胞瘤的高度侵袭性形式有关。尽管各种临床前研究和临床试验表明有令人鼓舞的结果,但抗血管生成药物并未显著改善总体生存率(OS)。这表明需要发现新的治疗选择。胶质母细胞瘤是众多癌症之一,二甲双胍作为双胍类家族的抗高血糖药物,被用于治疗 2 型糖尿病(T2DM)的一线治疗药物,并且在体外和体内均具有抗肿瘤活性。基于这些发现,该药物已被重新应用,这表明抑制了许多致癌促进机制,并因此确定了涉及的分子途径。二甲双胍通过阻断 LKB1/AMPK/mTOR/S6K1 通路抑制癌细胞生长,导致 GSCs 选择性细胞死亡并抑制 CD133+细胞增殖。它对分化的胶质母细胞瘤细胞和正常人类干细胞的影响很小。系统检索 PubMed 上的信息。在对二甲双胍治疗胶质母细胞瘤的检索中发现了 106 篇文章。其中 6 篇是荟萃分析、随机对照试验、临床试验和系统评价。其余的都是文献综述文章。这些文章的年份是 2011 年至 2024 年。分离出合适的研究,并从每篇文章中理解并理解它们的重要信息,并将其输入数据库,从中获取本文使用的信息。在 clinicaltrials.gov 上搜索了关于二甲双胍治疗胶质母细胞瘤的临床试验。在本文中,我们检查和评估了二甲双胍对胶质母细胞瘤的潜在抗肿瘤作用,确定它是否可以作为一种适当的抗血管生成物质,并安全地添加到胶质母细胞瘤患者的治疗和管理中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8cbd/11171521/f6eb93da11fc/ijms-25-05694-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8cbd/11171521/f6eb93da11fc/ijms-25-05694-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8cbd/11171521/f6eb93da11fc/ijms-25-05694-g001.jpg

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