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静脉注射大剂量抗坏血酸治疗脑胶质瘤的研究进展(综述)。

Parenteral high‑dose ascorbate - A possible approach for the treatment of glioblastoma (Review).

机构信息

Department of Nutritional Biochemistry, University of Hohenheim, D‑70599 Stuttgart, Germany.

Pascoe Pharmazeutische Praeparate GmbH, D‑35394 Giessen, Germany.

出版信息

Int J Oncol. 2021 Jun;58(6). doi: 10.3892/ijo.2021.5215. Epub 2021 May 6.

DOI:10.3892/ijo.2021.5215
PMID:33955499
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8104923/
Abstract

For glioblastoma, the treatment with standard of care therapy comprising resection, radiation, and temozolomide results in overall survival of approximately 14-18 months after initial diagnosis. Even though several new therapy approaches are under investigation, it is difficult to achieve life prolongation and/or improvement of patient's quality of life. The aggressiveness and progression of glioblastoma is initially orchestrated by the biological complexity of its genetic phenotype and ability to respond to cancer therapy via changing its molecular patterns, thereby developing resistance. Recent clinical studies of pharmacological ascorbate have demonstrated its safety and potential efficacy in different cancer entities regarding patient's quality of life and prolongation of survival. In this review article, the actual glioblastoma treatment possibilities are summarized, the evidence for pharmacological ascorbate in glioblastoma treatment is examined and questions are posed to identify current gaps of knowledge regarding accessibility of ascorbate to the tumor area. Experiments with glioblastoma cell lines and tumor xenografts have demonstrated that high‑dose ascorbate induces cytotoxicity and oxidative stress largely selectively in malignant cells compared to normal cells suggesting ascorbate as a potential therapeutic agent. Further investigations in larger cohorts and randomized placebo‑controlled trials should be performed to confirm these findings as well as to improve delivery strategies to the brain, through the inherent barriers and ultimately to the malignant cells.

摘要

对于胶质母细胞瘤,采用标准治疗方案(包括手术切除、放疗和替莫唑胺化疗)治疗,在初始诊断后,患者的总体生存时间约为 14-18 个月。尽管有几种新的治疗方法正在研究中,但很难延长患者的生命和/或提高患者的生活质量。胶质母细胞瘤的侵袭性和进展性最初是由其遗传表型的生物学复杂性以及通过改变分子模式来响应癌症治疗的能力来协调的,从而产生耐药性。最近的药理学抗坏血酸临床研究表明,其在不同癌症实体中具有安全性和潜在疗效,可改善患者的生活质量并延长生存时间。在这篇综述文章中,总结了目前胶质母细胞瘤的治疗可能性,检查了药理学抗坏血酸在胶质母细胞瘤治疗中的证据,并提出了一些问题,以确定有关抗坏血酸进入肿瘤区域的可及性的当前知识空白。胶质母细胞瘤细胞系和肿瘤异种移植实验表明,与正常细胞相比,高剂量抗坏血酸在恶性细胞中诱导细胞毒性和氧化应激的选择性更强,这提示抗坏血酸可能是一种潜在的治疗药物。应该在更大的队列和随机安慰剂对照试验中进一步进行研究,以证实这些发现,并改进向大脑输送的策略,包括内在的障碍和最终到达恶性细胞。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a81/8104923/9982e3909db8/IJO-58-06-05215-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a81/8104923/dbbccf813ab9/IJO-58-06-05215-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a81/8104923/40487bba1361/IJO-58-06-05215-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a81/8104923/9982e3909db8/IJO-58-06-05215-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a81/8104923/dbbccf813ab9/IJO-58-06-05215-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a81/8104923/40487bba1361/IJO-58-06-05215-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a81/8104923/9982e3909db8/IJO-58-06-05215-g02.jpg

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