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纳米颗粒介导的胰腺癌基因递送与免疫调节疗法的新见解与展望

Novel insight and perspectives of nanoparticle-mediated gene delivery and immune-modulating therapies for pancreatic cancer.

作者信息

Wang Xinqiao, Yin Xue, Li Yuxin, Zhang Shuhui, Hu Meie, Wei Minjie, Li Zhenhua

机构信息

School of Pharmacy, China Medical University, Shenyang, Liaoning Province, 110122, P.R. China.

Department of Pharmacy, The First Hospital of China Medical University, Shenyang, Liaoning Province, 110001, P.R. China.

出版信息

J Nanobiotechnology. 2024 Dec 19;22(1):771. doi: 10.1186/s12951-024-02975-7.

DOI:10.1186/s12951-024-02975-7
PMID:39696302
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11656556/
Abstract

Current standard-of-care therapies have failed to improve the survival of patients with metastatic pancreatic cancer (PCA). Therefore, exploring novel therapeutic approaches for cancer targeting is of utmost need. During the past few years, many efforts have been made to develop conventional treatment strategies to reduce chemotherapy resistance. However, critical challenges have impeded current cancer management outcomes, and limited clinical responses have been achieved due to unfavorable off-target effects. Advances in nanotechnology-based gene and immune-modulator delivery systems have excellent advantages for improving the therapeutic efficacy of PCA and provide promising avenues for overcoming the immunosuppressive tumor microenvironment and enhancing patient treatment outcomes. This review article provides insight into the challenges, opportunities, and future perspectives of these novel emerging nanoparticles based on lipid, polymer, and inorganic metal carriers to modulate genes and immunotherapy paradigms for PCA anticancer activity.

摘要

目前的标准治疗方案未能提高转移性胰腺癌(PCA)患者的生存率。因此,探索针对癌症的新型治疗方法迫在眉睫。在过去几年中,人们为开发传统治疗策略以降低化疗耐药性付出了诸多努力。然而,关键挑战阻碍了当前癌症治疗的效果,由于不良的脱靶效应,临床反应有限。基于纳米技术的基因和免疫调节剂递送系统的进展在提高PCA的治疗效果方面具有显著优势,并为克服免疫抑制性肿瘤微环境和提高患者治疗效果提供了有前景的途径。这篇综述文章深入探讨了这些基于脂质、聚合物和无机金属载体的新型纳米颗粒在调节基因和免疫治疗模式以实现PCA抗癌活性方面所面临的挑战、机遇和未来前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/589c/11656556/aa6d11d9cf6d/12951_2024_2975_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/589c/11656556/3ab9cfd02884/12951_2024_2975_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/589c/11656556/039af50c1c7f/12951_2024_2975_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/589c/11656556/88028a3bb63c/12951_2024_2975_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/589c/11656556/d6a4b3cf1289/12951_2024_2975_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/589c/11656556/63aada70cab2/12951_2024_2975_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/589c/11656556/aa6d11d9cf6d/12951_2024_2975_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/589c/11656556/3ab9cfd02884/12951_2024_2975_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/589c/11656556/039af50c1c7f/12951_2024_2975_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/589c/11656556/88028a3bb63c/12951_2024_2975_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/589c/11656556/d6a4b3cf1289/12951_2024_2975_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/589c/11656556/63aada70cab2/12951_2024_2975_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/589c/11656556/aa6d11d9cf6d/12951_2024_2975_Fig6_HTML.jpg

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Co-delivery of gemcitabine and Triapine by calcium carbonate nanoparticles against chemoresistant pancreatic cancer.碳酸钙纳米粒载吉西他滨和三嗪胶联合化疗治疗耐药胰腺癌。
Int J Pharm. 2023 Apr 5;636:122844. doi: 10.1016/j.ijpharm.2023.122844. Epub 2023 Mar 14.
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Targeted siRNA lipid nanoparticles for the treatment of KRAS-mutant tumors.
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Nanoparticles of VAV1 siRNA combined with LL37 peptide for the treatment of pancreatic cancer.VAV1小干扰RNA纳米颗粒联合LL37肽用于治疗胰腺癌。
J Control Release. 2023 Mar;355:312-326. doi: 10.1016/j.jconrel.2023.01.084. Epub 2023 Feb 9.
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Target-Specific Nanoparticle Polyplex Down-Regulates Mutant to Prevent Pancreatic Carcinogenesis and Halt Tumor Progression.靶向纳米颗粒聚合物复合物下调突变 以预防胰腺癌发生和阻止肿瘤进展。
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Peptide-Based Nanoparticles for αvβ3 Integrin-Targeted DNA Delivery to Cancer and Uterine Leiomyoma Cells.基于肽的纳米粒子用于 αvβ3 整联蛋白靶向的 DNA 递送至癌细胞和子宫肌瘤细胞。
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