我们合作得更好吗?解决匹伐他汀和替莫唑胺联合治疗脑癌的问题。

IF 4.2 3区 医学 Q1 PHARMACOLOGY & PHARMACY
João Basso , Ana Miguel Matos , Saeid Ghavami , Ana Fortuna , Rui Vitorino , Carla Vitorino
{"title":"我们合作得更好吗?解决匹伐他汀和替莫唑胺联合治疗脑癌的问题。","authors":"João Basso ,&nbsp;Ana Miguel Matos ,&nbsp;Saeid Ghavami ,&nbsp;Ana Fortuna ,&nbsp;Rui Vitorino ,&nbsp;Carla Vitorino","doi":"10.1016/j.ejphar.2024.177087","DOIUrl":null,"url":null,"abstract":"<div><div>Pitavastatin is commonly prescribed to treat hypercholesterolemia through the regulation of cholesterol biosynthesis. Interestingly, it has also demonstrated a great potential for treating brain tumors, although the detailed cytotoxic mechanism, particularly in glioblastoma, remains incompletely understood. This work explores the activity of pitavastatin in 2D and 3D glioblastoma models, in an attempt to provide a more representative and robust overview of its anticancer potential in glioblastoma. The results show that not only is pitavastatin 10-1000 times-fold more effective in reducing tumoral metabolic activity than temozolomide, but also demonstrate a synergistic activity with this alkylating drug. In addition, low micromolar concentrations of this statin strongly impair the growth and the invasion ability of multicellular tumor spheroids. The obtained qRT-PCR and proteomics data highlight the modulation of cell death via apoptosis (<em>BAX/BCL2, CASP9</em>) and autophagy (<em>BECN1, BNIP3</em>, <em>BNIP3L</em> and <em>LC3B</em>), as well as an epithelial to mesenchymal transition blockage (HTRA1, SERPINE1, WNT5A, ALDH3B1 and EPHA2) and remodeling of the extracellular matrix (VCAN, SERPINE1 and TGFBI). Overall, these results lay the foundation for further investigations on the potential combinatory clinical treatment with temozolomide.</div></div>","PeriodicalId":12004,"journal":{"name":"European journal of pharmacology","volume":"985 ","pages":"Article 177087"},"PeriodicalIF":4.2000,"publicationDate":"2024-11-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Are we better together? Addressing a combined treatment of pitavastatin and temozolomide for brain cancer\",\"authors\":\"João Basso ,&nbsp;Ana Miguel Matos ,&nbsp;Saeid Ghavami ,&nbsp;Ana Fortuna ,&nbsp;Rui Vitorino ,&nbsp;Carla Vitorino\",\"doi\":\"10.1016/j.ejphar.2024.177087\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Pitavastatin is commonly prescribed to treat hypercholesterolemia through the regulation of cholesterol biosynthesis. Interestingly, it has also demonstrated a great potential for treating brain tumors, although the detailed cytotoxic mechanism, particularly in glioblastoma, remains incompletely understood. This work explores the activity of pitavastatin in 2D and 3D glioblastoma models, in an attempt to provide a more representative and robust overview of its anticancer potential in glioblastoma. The results show that not only is pitavastatin 10-1000 times-fold more effective in reducing tumoral metabolic activity than temozolomide, but also demonstrate a synergistic activity with this alkylating drug. In addition, low micromolar concentrations of this statin strongly impair the growth and the invasion ability of multicellular tumor spheroids. The obtained qRT-PCR and proteomics data highlight the modulation of cell death via apoptosis (<em>BAX/BCL2, CASP9</em>) and autophagy (<em>BECN1, BNIP3</em>, <em>BNIP3L</em> and <em>LC3B</em>), as well as an epithelial to mesenchymal transition blockage (HTRA1, SERPINE1, WNT5A, ALDH3B1 and EPHA2) and remodeling of the extracellular matrix (VCAN, SERPINE1 and TGFBI). Overall, these results lay the foundation for further investigations on the potential combinatory clinical treatment with temozolomide.</div></div>\",\"PeriodicalId\":12004,\"journal\":{\"name\":\"European journal of pharmacology\",\"volume\":\"985 \",\"pages\":\"Article 177087\"},\"PeriodicalIF\":4.2000,\"publicationDate\":\"2024-11-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"European journal of pharmacology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0014299924007775\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PHARMACOLOGY & PHARMACY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"European journal of pharmacology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0014299924007775","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0

摘要

匹伐他汀是通过调节胆固醇的生物合成来治疗高胆固醇血症的常用药物。有趣的是,它在治疗脑肿瘤方面也显示出巨大的潜力,尽管人们对其详细的细胞毒性机理,尤其是在胶质母细胞瘤中的机理仍不完全清楚。这项研究探讨了匹伐他汀在二维和三维胶质母细胞瘤模型中的活性,试图对其在胶质母细胞瘤中的抗癌潜力提供更具代表性和更有力的概述。结果表明,匹伐他汀在降低肿瘤代谢活性方面的效果不仅是替莫唑胺的10-1000倍,而且还显示出与这种烷化药物的协同活性。此外,低微摩尔浓度的他汀类药物会强烈影响多细胞肿瘤球体的生长和侵袭能力。获得的 qRT-PCR 和蛋白质组学数据强调了通过细胞凋亡(BAX/BCL2、CASP9)和自噬(BECN1、BNIP3、BNIP3L 和 LC3B)调节细胞死亡,以及阻止上皮细胞向间充质转化(HTRA1、SERPINE1、WNT5A、ALDH3B1 和 EPHA2)和重塑细胞外基质(VCAN、SERPINE1 和 TGFBI)。总之,这些结果为进一步研究替莫唑胺的潜在联合临床治疗奠定了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Are we better together? Addressing a combined treatment of pitavastatin and temozolomide for brain cancer

Are we better together? Addressing a combined treatment of pitavastatin and temozolomide for brain cancer
Pitavastatin is commonly prescribed to treat hypercholesterolemia through the regulation of cholesterol biosynthesis. Interestingly, it has also demonstrated a great potential for treating brain tumors, although the detailed cytotoxic mechanism, particularly in glioblastoma, remains incompletely understood. This work explores the activity of pitavastatin in 2D and 3D glioblastoma models, in an attempt to provide a more representative and robust overview of its anticancer potential in glioblastoma. The results show that not only is pitavastatin 10-1000 times-fold more effective in reducing tumoral metabolic activity than temozolomide, but also demonstrate a synergistic activity with this alkylating drug. In addition, low micromolar concentrations of this statin strongly impair the growth and the invasion ability of multicellular tumor spheroids. The obtained qRT-PCR and proteomics data highlight the modulation of cell death via apoptosis (BAX/BCL2, CASP9) and autophagy (BECN1, BNIP3, BNIP3L and LC3B), as well as an epithelial to mesenchymal transition blockage (HTRA1, SERPINE1, WNT5A, ALDH3B1 and EPHA2) and remodeling of the extracellular matrix (VCAN, SERPINE1 and TGFBI). Overall, these results lay the foundation for further investigations on the potential combinatory clinical treatment with temozolomide.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
9.00
自引率
0.00%
发文量
572
审稿时长
34 days
期刊介绍: The European Journal of Pharmacology publishes research papers covering all aspects of experimental pharmacology with focus on the mechanism of action of structurally identified compounds affecting biological systems. The scope includes: Behavioural pharmacology Neuropharmacology and analgesia Cardiovascular pharmacology Pulmonary, gastrointestinal and urogenital pharmacology Endocrine pharmacology Immunopharmacology and inflammation Molecular and cellular pharmacology Regenerative pharmacology Biologicals and biotherapeutics Translational pharmacology Nutriceutical pharmacology.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信