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将替莫唑胺整合和优化到标准胶质母细胞瘤治疗中:一项临床前研究。

Integrating and optimizing tonabersat in standard glioblastoma therapy: A preclinical study.

机构信息

Department of Radiology, Ghent University, Ghent, Belgium.

IBiTech-Medisip-Infinity lab, Ghent University, Ghent, Belgium.

出版信息

PLoS One. 2024 Mar 15;19(3):e0300552. doi: 10.1371/journal.pone.0300552. eCollection 2024.

Abstract

Glioblastoma (GB), a highly aggressive primary brain tumor, presents a poor prognosis despite the current standard therapy, including radiotherapy and temozolomide (TMZ) chemotherapy. Tumor microtubes involving connexin 43 (Cx43) contribute to glioma progression and therapy resistance, suggesting Cx43 inhibition as a potential treatment strategy. This research aims to explore the adjuvant potential of tonabersat, a Cx43 gap junction modulator and blood-brain barrier-penetrating compound, in combination with the standard of care for GB. In addition, different administration schedules and timings to optimize tonabersat's therapeutic window are investigated. The F98 Fischer rat model will be utilized to investigate tonabersat's impact in a clinically relevant setting, by incorporating fractionated radiotherapy (three fractions of 9 Gy) and TMZ chemotherapy (29 mg/kg). This study will evaluate tonabersat's impact on tumor growth, survival, and treatment response through advanced imaging (CE T1-w MRI) and histological analysis. Results show extended survival in rats receiving tonabersat with standard care, highlighting its adjuvant potential. Daily tonabersat administration, both preceding and following radiotherapy, emerges as a promising approach for maximizing survival outcomes. The study suggests tonabersat's potential to reduce tumor invasiveness, providing a new avenue for GB treatment. In conclusion, this preclinical investigation highlights tonabersat's potential as an effective adjuvant treatment for GB, and its established safety profile from clinical trials in migraine treatment presents a promising foundation for further exploration.

摘要

胶质母细胞瘤(GB)是一种高度侵袭性的原发性脑肿瘤,尽管目前的标准治疗包括放疗和替莫唑胺(TMZ)化疗,但预后仍然不佳。涉及连接蛋白 43(Cx43)的肿瘤微管有助于胶质瘤的进展和治疗耐药性,表明 Cx43 抑制可能是一种潜在的治疗策略。本研究旨在探讨 Cx43 间隙连接调节剂和血脑屏障穿透化合物托纳布沙与 GB 标准治疗联合的辅助潜力。此外,还研究了不同的给药方案和时间,以优化托纳布沙的治疗窗口。利用 F98 Fisher 大鼠模型,通过分次放疗(3 次 9 Gy)和 TMZ 化疗(29 mg/kg),在临床相关环境中研究托纳布沙的作用。该研究将通过先进的成像(CE T1-w MRI)和组织学分析评估托纳布沙对肿瘤生长、生存和治疗反应的影响。结果表明,接受托纳布沙联合标准治疗的大鼠生存时间延长,突出了其辅助潜力。放疗前后每日给予托纳布沙是提高生存结果的一种有前途的方法。该研究表明托纳布沙有潜力降低肿瘤侵袭性,为 GB 治疗提供了新途径。总之,这项临床前研究强调了托纳布沙作为胶质母细胞瘤有效辅助治疗的潜力,其在偏头痛治疗中的临床试验确立的安全性为进一步探索提供了有希望的基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0bd2/10942024/2e1c925b846b/pone.0300552.g001.jpg

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