一种提高胶质母细胞瘤多形性治疗效果的新方法:非编码RNA靶向治疗和辅助方法。

IF 4.4 2区 医学 Q1 GENETICS & HEREDITY
Meijun Liu, Yuying Wang, Xiaoli Chen, Yu Zeng, Wenqiong Huang, Jiawen Yang, Hong Dai, Lixin Cheng, Claudio Mauro, Kenneth Chat Pan Cheung
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引用次数: 0

摘要

背景:多形性胶质母细胞瘤是一种致死性脑肿瘤。使用目前的金标准化疗药物替莫唑胺(TMZ),许多患者存活时间不超过一年。虽然研究新疗法的紧迫性是可以理解的,但过高的成本以及研究和临床试验的持续时间过长,大大推迟了向公众提供医学进步的时间。这凸显了迫切需要辅助治疗来提高治疗效果。正文:最近的研究表明,fda批准的药物如替莫唑胺(TMZ)、双硫仑(DSF)和阿司匹林有可能用于治疗胶质母细胞瘤,特别是DSF和阿司匹林的证据令人鼓舞。此外,像组蛋白去乙酰化酶抑制剂(如伏立诺他)这样的化合物正在研究它们对非编码RNA (ncRNA)调节的影响,包括微RNA (miRNAs)和长链非编码RNA (lncRNAs)。将传统疗法与ncRNA调节相结合,在提高治疗效果和靶向特异性方面显示出潜力。NcRNAs在调节基因表达中起着至关重要的作用,并与肿瘤的生长、侵袭和治疗抵抗有关。最近的发现,如铜增生,为肿瘤细胞死亡机制提供了新的见解。结论:本文综述了这些分子信息如何作为新的治疗靶点,以及药物辅助治疗如何改善GBM的治疗策略。重点关注ncRNA调控与常规治疗的整合以及增强药物疗效的联合策略如何提高治疗效果,为GBM治疗的创新方法铺平道路。简而言之,我们将探讨非编码rna (ncRNAs)如何作为有希望的靶点,以及如何重新利用TMZ、DSF和阿司匹林来帮助提高GBM治疗的疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A novel approach to enhance glioblastoma multiforme treatment efficacy: non-coding RNA targeted therapy and adjuvant approaches.

A novel approach to enhance glioblastoma multiforme treatment efficacy: non-coding RNA targeted therapy and adjuvant approaches.

A novel approach to enhance glioblastoma multiforme treatment efficacy: non-coding RNA targeted therapy and adjuvant approaches.

A novel approach to enhance glioblastoma multiforme treatment efficacy: non-coding RNA targeted therapy and adjuvant approaches.

Background: Glioblastoma multiforme (GBM) is a lethal brain tumor. With the current gold standard chemotherapy treatment, temozolomide (TMZ), many patients do not survive beyond one year. While the urgency of researching novel treatments is understandable, the prohibitively high costs and the prolonged duration of research and clinical trials significantly delay the availability of medical advancements to the general public. This highlights the urgent need for adjuvant therapies to enhance treatment effectiveness.

Main body: Recent research has suggested the potential of repurposing FDA-approved drugs such as temozolomide (TMZ), disulfiram (DSF), and aspirin for the treatment of glioblastoma, with encouraging evidence particularly for DSF and aspirin. Additionally, compounds like histone deacetylase inhibitors (e.g., vorinostat) are being investigated for their impact on non-coding RNA (ncRNA) modulation, including microRNAs (miRNAs) and long non-coding RNAs (lncRNAs). Combining traditional therapies with ncRNA modulation has shown potential in enhancing therapeutic efficacy and targeting specificity. NcRNAs play a crucial role in regulating gene expression and have been implicated in tumor growth, invasion, and treatment resistance. Recent discoveries, such as cuproptosis, offer new insights into tumor cell death mechanisms.

Conclusion: This review focuses on how these molecular insights can serve as novel therapeutic targets and how drug adjuvant therapy may improve GBM treatment strategies. It focuses on how the integration of ncRNA modulation with conventional therapies and the combination strategy of enhancing efficacy of drugs can enhance treatment efficacy and pave the way for innovative approaches in managing GBM. In short, we will explore how non-coding RNAs (ncRNAs) might serve as promising targets and how repurposing TMZ, DSF, and aspirin could help enhance the efficacy of GBM treatment.

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来源期刊
自引率
5.30%
发文量
150
期刊介绍: Clinical Epigenetics, the official journal of the Clinical Epigenetics Society, is an open access, peer-reviewed journal that encompasses all aspects of epigenetic principles and mechanisms in relation to human disease, diagnosis and therapy. Clinical trials and research in disease model organisms are particularly welcome.
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