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铁死亡在胶质母细胞瘤治疗中的作用。

Ferroptosis Involvement in Glioblastoma Treatment.

机构信息

Department of Morphological Sciences, Iuliu Hațieganu University of Medicine and Pharmacy, 8 Victor Babes Street, 400012 Cluj-Napoca, Romania.

Department of Neurosurgery, Iuliu Hațieganu University of Medicine and Pharmacy, 8 Victor Babes Street, 400012 Cluj-Napoca, Romania.

出版信息

Medicina (Kaunas). 2022 Feb 20;58(2):319. doi: 10.3390/medicina58020319.

DOI:10.3390/medicina58020319
PMID:35208642
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8876121/
Abstract

Glioblastoma multiforme (GBM) is one of the deadliest brain tumors. Current standard therapy includes tumor resection surgery followed by radiotherapy and chemotherapy. Due to the tumors invasive nature, recurrences are almost a certainty, giving the patients after diagnosis only a 12-15 months average survival time. Therefore, there is a dire need of finding new therapies that could potentially improve patient outcomes. Ferroptosis is a newly described form of cell death with several implications in cancer, among which GBM. Agents that target different molecules involved in ferroptosis and that stimulate this process have been described as potentially adjuvant anti-cancer treatment options. In GBM, ferroptosis stimulation inhibits tumor growth, improves patient survival, and increases the efficacy of radiation and chemotherapy. This review provides an overview of the current knowledge regarding ferroptosis modulation in GBM.

摘要

胶质母细胞瘤(GBM)是最致命的脑肿瘤之一。目前的标准治疗包括肿瘤切除术,然后进行放疗和化疗。由于肿瘤的侵袭性,复发几乎是必然的,这使得患者诊断后的平均存活时间仅为 12-15 个月。因此,迫切需要寻找新的治疗方法,以提高患者的治疗效果。铁死亡是一种新描述的细胞死亡形式,在癌症中有多种意义,包括 GBM。靶向铁死亡过程中涉及的不同分子并刺激这一过程的药物已被描述为潜在的辅助抗癌治疗选择。在 GBM 中,铁死亡刺激可抑制肿瘤生长,提高患者生存率,并增加放疗和化疗的疗效。这篇综述概述了目前关于 GBM 中铁死亡调节的知识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/131d/8876121/47bf6dab50fb/medicina-58-00319-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/131d/8876121/567279228e7d/medicina-58-00319-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/131d/8876121/47bf6dab50fb/medicina-58-00319-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/131d/8876121/567279228e7d/medicina-58-00319-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/131d/8876121/47bf6dab50fb/medicina-58-00319-g002.jpg

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Overexpression of Cystine/Glutamate Antiporter xCT Correlates with Nutrient Flexibility and ZEB1 Expression in Highly Clonogenic Glioblastoma Stem-like Cells (GSCs).
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Glioma stem cells remodel immunotolerant microenvironment in GBM and are associated with therapeutic advancements.神经胶质瘤干细胞重塑胶质母细胞瘤中的免疫耐受微环境,并与治疗进展相关。
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Glioblastoma mesenchymal subtype enhances antioxidant defence to reduce susceptibility to ferroptosis.胶质母细胞瘤间质亚型增强抗氧化防御能力,降低铁死亡敏感性。
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