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脂质纳米粒在结直肠癌治疗中的研究进展。

Research Advances of Lipid Nanoparticles in the Treatment of Colorectal Cancer.

机构信息

Department of Surgery, The Fourth Affiliated Hospital of School of Medicine, and International School of Medicine, International Institutes of Medicine, Zhejiang University, Yiwu, People's Republic of China.

Department of Colorectal Surgery and Oncology, Key Laboratory of Cancer Prevention and Intervention, Ministry of Education, 2nd Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, People's Republic of China.

出版信息

Int J Nanomedicine. 2024 Jul 3;19:6693-6715. doi: 10.2147/IJN.S466490. eCollection 2024.


DOI:10.2147/IJN.S466490
PMID:38979534
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11229238/
Abstract

Colorectal cancer (CRC) is a common type of gastrointestinal tract (GIT) cancer and poses an enormous threat to human health. Current strategies for metastatic colorectal cancer (mCRC) therapy primarily focus on chemotherapy, targeted therapy, immunotherapy, and radiotherapy; however, their adverse reactions and drug resistance limit their clinical application. Advances in nanotechnology have rendered lipid nanoparticles (LNPs) a promising nanomaterial-based drug delivery system for CRC therapy. LNPs can adapt to the biological characteristics of CRC by modifying their formulation, enabling the selective delivery of drugs to cancer tissues. They overcome the limitations of traditional therapies, such as poor water solubility, nonspecific biodistribution, and limited bioavailability. Herein, we review the composition and targeting strategies of LNPs for CRC therapy. Subsequently, the applications of these nanoparticles in CRC treatment including drug delivery, thermal therapy, and nucleic acid-based gene therapy are summarized with examples provided. The last section provides a glimpse into the advantages, current limitations, and prospects of LNPs in the treatment of CRC.

摘要

结直肠癌(CRC)是一种常见的胃肠道(GIT)癌症,对人类健康构成巨大威胁。目前转移性结直肠癌(mCRC)治疗的策略主要集中在化疗、靶向治疗、免疫治疗和放疗上;然而,它们的不良反应和耐药性限制了它们的临床应用。纳米技术的进步使脂质纳米粒(LNPs)成为一种很有前途的基于纳米材料的 CRC 治疗药物输送系统。LNPs 通过改变其配方来适应 CRC 的生物学特性,使药物能够选择性地输送到癌症组织。它们克服了传统疗法的局限性,如水溶性差、非特异性生物分布和有限的生物利用度。在此,我们综述了 LNPs 用于 CRC 治疗的组成和靶向策略。随后,我们通过实例总结了这些纳米粒子在 CRC 治疗中的应用,包括药物输送、热疗和基于核酸的基因治疗。最后一部分介绍了 LNPs 在 CRC 治疗中的优势、当前的局限性和前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/218f/11229238/5065f3341ed9/IJN-19-6693-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/218f/11229238/3d53d375c4c9/IJN-19-6693-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/218f/11229238/f500e8a9b03f/IJN-19-6693-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/218f/11229238/a5141f1fa387/IJN-19-6693-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/218f/11229238/636b83c11d2b/IJN-19-6693-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/218f/11229238/1c046e2623ba/IJN-19-6693-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/218f/11229238/a5c6e7e1a56e/IJN-19-6693-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/218f/11229238/5065f3341ed9/IJN-19-6693-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/218f/11229238/3d53d375c4c9/IJN-19-6693-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/218f/11229238/f500e8a9b03f/IJN-19-6693-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/218f/11229238/a5141f1fa387/IJN-19-6693-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/218f/11229238/636b83c11d2b/IJN-19-6693-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/218f/11229238/1c046e2623ba/IJN-19-6693-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/218f/11229238/a5c6e7e1a56e/IJN-19-6693-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/218f/11229238/5065f3341ed9/IJN-19-6693-g0007.jpg

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引用本文的文献

[1]
Yi Gong San inhibits tumor immune escape by sensitizing colorectal cancer stem cells via the NF-κB pathway.

Hereditas. 2025-4-17

[2]
Nano-Radiopharmaceuticals in Colon Cancer: Current Applications, Challenges, and Future Directions.

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[3]
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本文引用的文献

[1]
Conventional vs PEGylated loaded liposomal formulations by microfluidics for delivering hydrophilic chemotherapy.

Int J Pharm. 2024-4-25

[2]
Engineering LNPs with polysarcosine lipids for mRNA delivery.

Bioact Mater. 2024-3-16

[3]
Ionizable Lipid Nanoparticle-Mediated TRAIL mRNA Delivery in the Tumor Microenvironment to Inhibit Colon Cancer Progression.

Int J Nanomedicine. 2024

[4]
pH-Dependent Lyotropic Liquid Crystalline Mesophase and Ionization Behavior of Phytantriol-Based Ionizable Lipid Nanoparticles.

Small. 2024-5

[5]
Exploring the role of sporadic BRAF and KRAS mutations during colorectal cancer pathogenesis: A spotlight on the contribution of the endosome-lysosome system.

Cancer Lett. 2024-3-31

[6]
Strategies to reduce the risks of mRNA drug and vaccine toxicity.

Nat Rev Drug Discov. 2024-4

[7]
Biological recognition and cellular trafficking of targeted RNA-lipid nanoparticles.

Curr Opin Biotechnol. 2024-2

[8]
Organometallic Phyllosilicate-Gold Nanocomplex: An Effective Oral Delivery System of Methotrexate for Enhanced in vivo Efficacy Against Colorectal Cancer.

Int J Nanomedicine. 2023

[9]
Micro-syringe chip-guided intratumoral administration of lipid nanoparticles for targeted anticancer therapy.

Biomater Res. 2023-10-16

[10]
USP51 facilitates colorectal cancer stemness and chemoresistance by forming a positive feed-forward loop with HIF1A.

Cell Death Differ. 2023-11

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