Tailor-made vincristine-liposomes for tumor targeting.

Ariana Abawi, Ana-Maria Trunfio-Sfarghiu, Céline Thomann, Emma Petiot, Giovanna Lollo, Thierry Granjon, Agnès Girard-Egrot, Ofelia Maniti
{"title":"Tailor-made vincristine-liposomes for tumor targeting.","authors":"Ariana Abawi, Ana-Maria Trunfio-Sfarghiu, Céline Thomann, Emma Petiot, Giovanna Lollo, Thierry Granjon, Agnès Girard-Egrot, Ofelia Maniti","doi":"10.1016/j.biochi.2024.07.017","DOIUrl":null,"url":null,"abstract":"<p><p>To ensure selective targeting based on membrane fluidity and physico-chemical compatibility between the biological membrane of the target cell and the lipid membrane of the liposomes carriers. Lipid-based carriers as liposomes with varying membrane fluidities were designed for delivering vincristine, an anti-tumor compound derived from Madagascar's periwinkle. Liposomes, loaded with vincristine, were tested on prostate, colon, and breast cancer cell lines alongside non-tumor controls. Results showed that vincristine-loaded liposomes with fluid membranes significantly decreased the viability of cancer cell lines compared to controls. Confocal microscopy revealed the intracellular release of vincristine, evidenced by disrupted mitosis-specific labeling of actin filaments in metastatic prostate cell lines. This highlights the crucial role of membrane fluidity in the development of lipid-based drug carriers, offering a promising and cost-effective option for targeting cancer cells as an alternative to conventional strategies.</p>","PeriodicalId":93898,"journal":{"name":"Biochimie","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-07-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biochimie","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/j.biochi.2024.07.017","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

To ensure selective targeting based on membrane fluidity and physico-chemical compatibility between the biological membrane of the target cell and the lipid membrane of the liposomes carriers. Lipid-based carriers as liposomes with varying membrane fluidities were designed for delivering vincristine, an anti-tumor compound derived from Madagascar's periwinkle. Liposomes, loaded with vincristine, were tested on prostate, colon, and breast cancer cell lines alongside non-tumor controls. Results showed that vincristine-loaded liposomes with fluid membranes significantly decreased the viability of cancer cell lines compared to controls. Confocal microscopy revealed the intracellular release of vincristine, evidenced by disrupted mitosis-specific labeling of actin filaments in metastatic prostate cell lines. This highlights the crucial role of membrane fluidity in the development of lipid-based drug carriers, offering a promising and cost-effective option for targeting cancer cells as an alternative to conventional strategies.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
"用于肿瘤靶向的定制长春新碱脂质体"。
根据膜流动性以及靶细胞生物膜与脂质体载体脂膜之间的物理化学相容性,确保选择性靶向。我们设计了具有不同膜流动性的脂质体载体,用于输送长春新碱(一种从马达加斯加长春花中提取的抗肿瘤化合物)。负载长春新碱的脂质体在前列腺癌、结肠癌和乳腺癌细胞系以及非肿瘤对照组中进行了测试。结果表明,与对照组相比,负载长春新碱的液膜脂质体能显著降低癌细胞株的存活率。共聚焦显微镜显示了长春新碱在细胞内的释放,转移性前列腺癌细胞系中肌动蛋白丝的有丝分裂特异性标记被破坏就是证明。这凸显了膜流动性在开发脂质药物载体中的关键作用,为靶向癌细胞提供了一种替代传统策略的前景广阔、成本效益高的选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Complete analysis of G-quadruplex forming sequences in the gapless assembly of human chromosome Y. The effect of extremolytes ectoine and hydroxyectoine on the heat-induced protein aggregation: The case of growth hormone. In vitro and in vivo evidence of the antineoplastic activity of quercetin against endothelial cells transformed by Kaposi's sarcoma-associated herpesvirus G protein-coupled receptor. Structural extracellular matrix-mediated molecular signaling in wound repair and tissue regeneration. A yummy blend of homeostasis and proteolytic mechanisms.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1