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近年来用于癌症治疗的药物-核酸联合递药系统的研究进展。

Recent advances in delivery of drug-nucleic acid combinations for cancer treatment.

机构信息

Department of Pharmaceutical Sciences and Center for Drug Delivery and Nanomedicine, University of Nebraska Medical Center, Omaha, NE 68198-5830, USA.

出版信息

J Control Release. 2013 Dec 10;172(2):589-600. doi: 10.1016/j.jconrel.2013.04.010. Epub 2013 Apr 25.

DOI:10.1016/j.jconrel.2013.04.010
PMID:23624358
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3783568/
Abstract

Cancer treatment that uses a combination of approaches with the ability to affect multiple disease pathways has been proven highly effective in the treatment of many cancers. Combination therapy can include multiple chemotherapeutics or combinations of chemotherapeutics with other treatment modalities like surgery or radiation. However, despite the widespread clinical use of combination therapies, relatively little attention has been given to the potential of modern nanocarrier delivery methods, like liposomes, micelles, and nanoparticles, to enhance the efficacy of combination treatments. This lack of knowledge is particularly notable in the limited success of vectors for the delivery of combinations of nucleic acids with traditional small molecule drugs. The delivery of drug-nucleic acid combinations is particularly challenging due to differences in the physicochemical properties of the two types of agents. This review discusses recent advances in the development of delivery methods using combinations of small molecule drugs and nucleic acid therapeutics to treat cancer. This review primarily focuses on the rationale used for selecting appropriate drug-nucleic acid combinations as well as progress in the development of nanocarriers suitable for simultaneous delivery of drug-nucleic acid combinations.

摘要

癌症治疗采用多种方法结合,能够影响多种疾病途径,已被证明对多种癌症的治疗非常有效。联合治疗可以包括多种化疗药物或化疗药物与手术或放疗等其他治疗方式的组合。然而,尽管联合治疗在临床上广泛应用,但人们对现代纳米载体传递方法(如脂质体、胶束和纳米颗粒)增强联合治疗效果的潜力关注甚少。这种知识的缺乏在用于传递核酸与传统小分子药物组合的载体的有限成功中尤为明显。由于两种类型的药物在理化性质上存在差异,因此药物-核酸组合的传递尤其具有挑战性。本文综述了使用小分子药物和核酸治疗药物联合治疗癌症的递药方法的最新进展。本文主要侧重于选择合适的药物-核酸组合的基本原理,以及开发适合同时递药-核酸组合的纳米载体的进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db83/3783568/b793714d1f84/nihms472544f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db83/3783568/faecc9f54640/nihms472544f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db83/3783568/4c9ba62770e7/nihms472544f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db83/3783568/10a959746346/nihms472544f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db83/3783568/b793714d1f84/nihms472544f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db83/3783568/faecc9f54640/nihms472544f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db83/3783568/4c9ba62770e7/nihms472544f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db83/3783568/10a959746346/nihms472544f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db83/3783568/b793714d1f84/nihms472544f4.jpg

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本文引用的文献

1
Systemic TNFα gene therapy synergizes with liposomal doxorubicine in the treatment of metastatic cancer.系统 TNFα 基因治疗与脂质体多柔比星联合治疗转移性癌症。
Mol Ther. 2013 Feb;21(2):300-8. doi: 10.1038/mt.2012.229. Epub 2012 Nov 13.
2
Lipid modified triblock PAMAM-based nanocarriers for siRNA drug co-delivery.用于 siRNA 药物共递送的脂质修饰的三嵌段 PAMAM 基纳米载体。
Biomaterials. 2013 Jan;34(4):1289-301. doi: 10.1016/j.biomaterials.2012.10.024. Epub 2012 Nov 5.
3
Co-delivery of doxorubicin and siRNA using octreotide-conjugated gold nanorods for targeted neuroendocrine cancer therapy.
基于自噬的肝细胞癌治疗:从标准治疗到联合治疗、溶瘤病毒疗法和靶向纳米药物。
Clin Exp Med. 2024 Dec 2;25(1):13. doi: 10.1007/s10238-024-01527-5.
4
Therapeutic types and advantages of functionalized nanoparticles in inducing ferroptosis in cancer therapy.功能化纳米颗粒在诱导癌症治疗中铁死亡中的治疗类型和优势。
Ann Med. 2024 Dec;56(1):2396568. doi: 10.1080/07853890.2024.2396568. Epub 2024 Sep 14.
5
Joining Forces: The Combined Application of Therapeutic Viruses and Nanomaterials in Cancer Therapy.联合出击:治疗性病毒与纳米材料在癌症治疗中的联合应用。
Molecules. 2023 Nov 20;28(22):7679. doi: 10.3390/molecules28227679.
6
Nanoparticles design considerations to co-deliver nucleic acids and anti-cancer drugs for chemoresistance reversal.用于逆转化疗耐药性的核酸和抗癌药物共递送的纳米颗粒设计考量
Int J Pharm X. 2022 Sep 6;4:100126. doi: 10.1016/j.ijpx.2022.100126. eCollection 2022 Dec.
7
New paradigm in combination therapy of siRNA with chemotherapeutic drugs for effective cancer therapy.用于有效癌症治疗的siRNA与化疗药物联合治疗的新范式。
Curr Res Pharmacol Drug Discov. 2022 Apr 28;3:100103. doi: 10.1016/j.crphar.2022.100103. eCollection 2022.
8
Co-delivery of doxorubicin and shRNA of Beclin1 by folate receptor targeted pullulan-based multifunctional nanomicelles for combinational cancer therapy.通过叶酸受体靶向的基于普鲁兰多糖的多功能纳米胶束共递送阿霉素和Beclin1的短发夹RNA用于联合癌症治疗
RSC Adv. 2018 May 15;8(32):17710-17722. doi: 10.1039/c8ra01679h. eCollection 2018 May 14.
9
Multifunctional Lipid Bilayer Nanocarriers for Cancer Immunotherapy in Heterogeneous Tumor Microenvironments, Combining Immunogenic Cell Death Stimuli with Immune Modulatory Drugs.多功能脂质双层纳米载体用于异质性肿瘤微环境中的癌症免疫治疗,将免疫原性细胞死亡刺激剂与免疫调节药物相结合。
ACS Nano. 2022 Apr 26;16(4):5184-5232. doi: 10.1021/acsnano.2c01252. Epub 2022 Mar 29.
10
Modified Gold Nanoparticles to Overcome the Chemoresistance to Gemcitabine in Mutant p53 Cancer Cells.修饰金纳米颗粒以克服突变型p53癌细胞对吉西他滨的化疗耐药性。
Pharmaceutics. 2021 Dec 3;13(12):2067. doi: 10.3390/pharmaceutics13122067.
奥曲肽偶联金纳米棒共递送阿霉素和 siRNA 用于神经内分泌肿瘤的靶向治疗。
Nanoscale. 2012 Nov 21;4(22):7185-93. doi: 10.1039/c2nr31853a.
4
In vitro and in vivo evaluation of the efficacy of nanoformulation of siRNA as an adjuvant to improve the anticancer potential of cisplatin.体外和体内评价 siRNA 纳米制剂作为佐剂提高顺铂抗癌潜力的疗效。
Exp Mol Pathol. 2013 Feb;94(1):137-47. doi: 10.1016/j.yexmp.2012.10.007. Epub 2012 Oct 10.
5
Targeting JNK-interacting-protein-1 (JIP1) sensitises osteosarcoma to doxorubicin.靶向JNK相互作用蛋白1(JIP1)可使骨肉瘤对多柔比星敏感。
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Targeting Notch, a key pathway for ovarian cancer stem cells, sensitizes tumors to platinum therapy.靶向 Notch,一种卵巢癌细胞干关键通路,可提高肿瘤对铂类治疗的敏感性。
Proc Natl Acad Sci U S A. 2012 Oct 23;109(43):E2939-48. doi: 10.1073/pnas.1206400109. Epub 2012 Sep 27.
7
Monodisperse double-walled microspheres loaded with chitosan-p53 nanoparticles and doxorubicin for combined gene therapy and chemotherapy.载有壳聚糖-p53 纳米粒和阿霉素的单分散双层微球用于联合基因治疗和化疗。
J Control Release. 2012 Oct 28;163(2):130-5. doi: 10.1016/j.jconrel.2012.08.032. Epub 2012 Sep 7.
8
Induction of apoptosis and sensitization of head and neck squamous carcinoma cells to cisplatin by targeting survivin gene expression.通过靶向生存素基因表达诱导细胞凋亡并增强头颈部鳞状细胞癌细胞对顺铂的敏感性。
Curr Gene Ther. 2012 Dec;12(6):444-53. doi: 10.2174/156652312803519805.
9
Overcoming drug resistance of MCF-7/ADR cells by altering intracellular distribution of doxorubicin via MVP knockdown with a novel siRNA polyamidoamine-hyaluronic acid complex.通过新型 siRNA 聚酰胺-透明质酸复合物使 MVP 敲低从而改变阿霉素在 MCF-7/ADR 细胞内的分布,克服 MCF-7/ADR 细胞的耐药性。
J Control Release. 2012 Oct 28;163(2):136-44. doi: 10.1016/j.jconrel.2012.08.020. Epub 2012 Aug 23.
10
Inhibition of STAT3 reverses drug resistance acquired in temozolomide-resistant human glioma cells.抑制信号转导和转录激活因子3(STAT3)可逆转替莫唑胺耐药的人胶质瘤细胞中获得的耐药性。
Oncol Lett. 2011 Jan;2(1):115-121. doi: 10.3892/ol.2010.210. Epub 2010 Nov 23.