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用于递送癌症抗血管生成药物的纳米治疗制剂

Nanotherapeutic Formulations for the Delivery of Cancer Antiangiogenics.

作者信息

Ultimo Amelia, Jain Ayushi, Gomez-Gonzalez Elisabet, Alex Thomson Santosh, Moreno-Borrallo Almudena, Jana Sukanya, Ghosh Shubhrima, Ruiz-Hernandez Eduardo

机构信息

School of Pharmacy and Pharmaceutical Sciences, Trinity College Dublin, the University of Dublin, College Green, Dublin 2 D02 PN40, Ireland.

Trinity Translational Medicine Institute, Trinity College Dublin, the University of Dublin, St. James's Hospital, Dublin 8 D08 NHY1, Ireland.

出版信息

Mol Pharm. 2025 May 5;22(5):2322-2349. doi: 10.1021/acs.molpharmaceut.4c00822. Epub 2025 Apr 4.

DOI:10.1021/acs.molpharmaceut.4c00822
PMID:40184281
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12056699/
Abstract

Antiangiogenic medications for cancer treatment have generally failed in showing substantial benefits in terms of prolonging life on their own; their effects are noticeable only when combined with chemotherapy. Moreover, treatments based on prolonged antiangiogenics administration have demonstrated to be ineffective in stopping tumor progression. In this scenario, nanotherapeutics can address certain issues linked to existing antiangiogenic treatments. More specifically, they can provide the ability to target the tumor's blood vessels to enhance drug accumulation and manage release, ultimately decreasing undesired side effects. Additionally, they enable the administration of multiple angiogenesis inhibitors at the same time as chemotherapy. Key reports in this field include the design of polymeric nanoparticles, inorganic nanoparticles, vesicles, and hydrogels for loading antiangiogenic substances like endostatin and interleukin-12. Furthermore, nanoformulations have been proposed to efficiently control relevant pro-angiogenic pathways such as VEGF, Tie2/Angiopoietin-1, HIF-1α/HIF-2α, and TGF-β, providing powerful approaches to block tumor growth and metastasis. In this article, we outline a selection of nanoformulations for antiangiogenic treatments for cancer that have been developed in the past ten years.

摘要

用于癌症治疗的抗血管生成药物通常未能单独在延长生命方面显示出显著益处;只有与化疗联合使用时其效果才明显。此外,基于长期给予抗血管生成药物的治疗已证明在阻止肿瘤进展方面无效。在这种情况下,纳米疗法可以解决与现有抗血管生成治疗相关的某些问题。更具体地说,它们能够靶向肿瘤血管以增强药物积累和控制释放,最终减少不良副作用。此外,它们能够在化疗的同时给予多种血管生成抑制剂。该领域的关键报道包括用于负载内皮抑素和白细胞介素 - 12等抗血管生成物质的聚合物纳米颗粒、无机纳米颗粒、囊泡和水凝胶的设计。此外,已提出纳米制剂以有效控制相关的促血管生成途径,如血管内皮生长因子(VEGF)、酪氨酸激酶2/血管生成素 - 1(Tie2/Angiopoietin - 1)、缺氧诱导因子 - 1α/缺氧诱导因子 - 2α(HIF - 1α/HIF - 2α)和转化生长因子 - β(TGF - β),提供了阻断肿瘤生长和转移的有力方法。在本文中,我们概述了过去十年中开发的用于癌症抗血管生成治疗的一系列纳米制剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62ba/12056699/7a605622a48a/mp4c00822_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62ba/12056699/ae797c4b473e/mp4c00822_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62ba/12056699/af8b7729e599/mp4c00822_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62ba/12056699/24ce44ec9a73/mp4c00822_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62ba/12056699/cdf32b2837c8/mp4c00822_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62ba/12056699/bfb401f712dc/mp4c00822_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62ba/12056699/7a605622a48a/mp4c00822_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62ba/12056699/ae797c4b473e/mp4c00822_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62ba/12056699/af8b7729e599/mp4c00822_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62ba/12056699/24ce44ec9a73/mp4c00822_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62ba/12056699/cdf32b2837c8/mp4c00822_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62ba/12056699/bfb401f712dc/mp4c00822_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62ba/12056699/7a605622a48a/mp4c00822_0006.jpg

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本文引用的文献

1
Endostatin in disease modulation: From cancer to beyond.内皮抑素在疾病调节中的作用:从癌症到其他领域。
Vascul Pharmacol. 2025 Mar;158:107459. doi: 10.1016/j.vph.2024.107459. Epub 2024 Dec 19.
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Chitosan-based nanoarchitectures for siRNA delivery in cancer therapy: A review of pre-clinical and clinical importance.用于癌症治疗中 siRNA 递送的基于壳聚糖的纳米结构:临床前和临床重要性综述
Int J Biol Macromol. 2025 Jan;284(Pt 1):137708. doi: 10.1016/j.ijbiomac.2024.137708. Epub 2024 Nov 20.
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Targeted Hybrid Nanocarriers as Co-Delivery Systems for Enhanced Cancer Therapy.
靶向杂化纳米载体作为增强癌症治疗的共递送系统
Adv Pharm Bull. 2024 Oct;14(3):558-573. doi: 10.34172/apb.2024.046. Epub 2024 May 15.
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Recent Applications of PLGA in Drug Delivery Systems.聚乳酸-羟基乙酸共聚物在药物递送系统中的最新应用
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The role of cancer-associated fibroblasts and exosomal miRNAs-mediated intercellular communication in the tumor microenvironment and the biology of carcinogenesis: a systematic review.癌症相关成纤维细胞和外泌体微小RNA介导的细胞间通讯在肿瘤微环境及致癌生物学中的作用:一项系统综述
Cell Death Discov. 2024 Aug 26;10(1):380. doi: 10.1038/s41420-024-02146-5.
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Advances in Medicine: Photodynamic Therapy.医学进展:光动力疗法。
Int J Mol Sci. 2024 Jul 29;25(15):8258. doi: 10.3390/ijms25158258.
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Targeting cytokine and chemokine signaling pathways for cancer therapy.针对细胞因子和趋化因子信号通路的癌症治疗。
Signal Transduct Target Ther. 2024 Jul 22;9(1):176. doi: 10.1038/s41392-024-01868-3.
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Notch signaling pathway in cancer: from mechanistic insights to targeted therapies. Notch 信号通路与癌症:从机制研究到靶向治疗。
Signal Transduct Target Ther. 2024 May 27;9(1):128. doi: 10.1038/s41392-024-01828-x.
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Incorporation of immunotherapies and nanomedicine to better normalize angiogenesis-based cancer treatment.将免疫疗法和纳米医学纳入其中,以更好地使基于血管生成的癌症治疗正常化。
Microvasc Res. 2024 Jul;154:104691. doi: 10.1016/j.mvr.2024.104691. Epub 2024 May 3.
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Inorganic nanoparticle-cored dendrimers for biomedical applications: A review.用于生物医学应用的无机纳米粒子核树枝状大分子:综述
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