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Activatable "Matryoshka" nanosystem delivery NgBR siRNA and control drug release for stepwise therapy and evaluate drug resistance cancer.

作者信息

Xu Xinzhi, Jin Chunxiang, Zhang Kai, Cao Yang, Liu Junjun, Zhang Yue, Ran Haitao, Jin Ying

机构信息

Department of Ultrasound, China-Japan Union Hospital of Jilin University, Changchun, Jilin, 130033, China.

State Key Laboratory of Supramolecular Structure and Materials College of Chemistry, Jilin University, Changchun, Jilin, 130012, China.

出版信息

Mater Today Bio. 2022 Mar 19;14:100245. doi: 10.1016/j.mtbio.2022.100245. eCollection 2022 Mar.


DOI:10.1016/j.mtbio.2022.100245
PMID:35345559
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8956824/
Abstract

Drug resistance is always a challenge in conquering breast cancer clinically. Recognition of drug resistance and enhancing the sensitivity of the tumor to chemotherapy is urgent. Herein, a dual-responsive multi-function "Matryoshka" nanosystem is designed, it activates in the tumor microenvironment, decomposes layer by layer, and release gene and drug in sequence. The cell is re-educated by NgBR siRNA first to regain the chemosensitivity through regulating the Akt pathway and inhibit ERα activation, then the drugs loaded in the core are controlled released to killing cells. Carbonized polymer dots are loaded into the nanosystem as an efficient bioimaging probe, due to the GE11 modification, the nanosystem can be a seeker to recognize and evaluate drug-resistance tumors by photoacoustic imaging. In the tumor-bearing mouse, the novel nanosystem firstly enhances the sensitivity to chemotherapy by knockdown NgBR, inducing a much higher reduction in NgBR up to 52.09%, then effectively inhibiting tumor growth by chemotherapy, tumor growth in nude mouse was inhibited by 70.22%. The nanosystem also can inhibit metastasis, prolong survival time, and evaluate tumor drug resistance by real-time imaging. Overall, based on regulating the key molecules of drug resistance, we created visualization nanotechnology and formatted new comprehensive plans with high bio-safety for tumor diagnosis and treatment, providing a personalized strategy to overcome drug resistance clinically.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c06e/8956824/e9cd3d9d8ee3/gr9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c06e/8956824/5de74e2de1d2/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c06e/8956824/5ffed0176944/sc1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c06e/8956824/f48e1d24da23/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c06e/8956824/b2f454ed34b7/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c06e/8956824/8cd8a5a890a4/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c06e/8956824/50f5e4ce39f3/sc2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c06e/8956824/316dc62ab937/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c06e/8956824/ed56ac7072f6/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c06e/8956824/af07028fe070/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c06e/8956824/72dd1a698d84/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c06e/8956824/abd91636eabd/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c06e/8956824/e9cd3d9d8ee3/gr9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c06e/8956824/5de74e2de1d2/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c06e/8956824/5ffed0176944/sc1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c06e/8956824/f48e1d24da23/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c06e/8956824/b2f454ed34b7/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c06e/8956824/8cd8a5a890a4/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c06e/8956824/50f5e4ce39f3/sc2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c06e/8956824/316dc62ab937/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c06e/8956824/ed56ac7072f6/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c06e/8956824/af07028fe070/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c06e/8956824/72dd1a698d84/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c06e/8956824/abd91636eabd/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c06e/8956824/e9cd3d9d8ee3/gr9.jpg

相似文献

[1]
Activatable "Matryoshka" nanosystem delivery NgBR siRNA and control drug release for stepwise therapy and evaluate drug resistance cancer.

Mater Today Bio. 2022-3-19

[2]
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[7]
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[8]
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[9]
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[10]
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J Nanobiotechnology. 2023-5-4

本文引用的文献

[1]
Recent Progress in the Synthesis and Applications of Composite Photocatalysts: A Critical Review.

Small Methods. 2022-2

[2]
Nanoengineered Neutrophils as a Cellular Sonosensitizer for Visual Sonodynamic Therapy of Malignant Tumors.

Adv Mater. 2022-4

[3]
A multifunctional chemical toolbox to engineer carbon dots for biomedical and energy applications.

Nat Nanotechnol. 2022-2

[4]
Peroxisome Proliferator-Activated Receptor-Gamma Reduces ER Stress and Inflammation via Targeting NGBR Expression.

Front Pharmacol. 2022-1-17

[5]
A multifunctional platinum(IV) and cyanine dye-based polyprodrug for trimodal imaging-guided chemo-phototherapy.

J Mater Chem B. 2022-2-16

[6]
Estrogenic Activity of Mycoestrogen (3,5,22)-Ergost-22-en-3-ol via Estrogen Receptor α-Dependent Signaling Pathways in MCF-7 Cells.

Molecules. 2021-12-22

[7]
Targeted delivery of PARP inhibitors to neuronal mitochondria via biomimetic engineered nanosystems in a mouse model of traumatic brain injury.

Acta Biomater. 2022-3-1

[8]
A novel targeted co-delivery nanosystem for enhanced ovarian cancer treatment via multidrug resistance reversion and mTOR-mediated signaling pathway.

J Nanobiotechnology. 2021-12-23

[9]
Co-Delivery of Paclitaxel and shMCL-1 by Folic Acid-Modified Nonviral Vector to Overcome Cancer Chemotherapy Resistance.

Small Methods. 2021-5

[10]
Controlled release nanoplatforms for three commonly used chemotherapeutics.

Mol Aspects Med. 2022-2

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