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Enhancing Therapeutic Efficacy in Cancer Treatment: Integrating Nanomedicine with Autophagy Inhibition Strategies.

作者信息

Walweel Nada, Aydin Omer

机构信息

Department of Biomedical Engineering, Erciyes University, Kayseri 38039, Turkey.

NanoThera Lab, ERFARMA-Drug Application and Research Center, Erciyes University, Kayseri 38280, Turkey.

出版信息

ACS Omega. 2024 Jun 18;9(26):27832-27852. doi: 10.1021/acsomega.4c02234. eCollection 2024 Jul 2.


DOI:10.1021/acsomega.4c02234
PMID:38973850
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11223161/
Abstract

The complicated stepwise lysosomal degradation process known as autophagy is in charge of destroying and eliminating damaged organelles and defective cytoplasmic components. This mechanism promotes metabolic adaptability and nutrition recycling. Autophagy functions as a quality control mechanism in cells that support homeostasis and redox balance under normal circumstances. However, the role of autophagy in cancer is controversial because, mostly depending on the stage of the tumor, it may either suppress or support the disease. While autophagy delays the onset of tumors and slows the dissemination of cancer in the early stages of tumorigenesis, numerous studies demonstrate that autophagy promotes the development and spread of tumors as well as the evolution and development of resistance to several anticancer drugs in advanced cancer stages. In this Review, we primarily emphasize the therapeutic role of autophagy inhibition in improving the treatment of multiple cancers and give a broad overview of how its inhibition modulates cancer responses. There have been various attempts to inhibit autophagy, including the use of autophagy inhibitor drugs, gene silencing therapy (RNA interference), and nanoparticles. In this Review, all these topics are thoroughly covered and illustrated by recent studies and field investigations.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a83b/11223161/903dd289178b/ao4c02234_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a83b/11223161/4c61678cacdf/ao4c02234_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a83b/11223161/2f96a4a55503/ao4c02234_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a83b/11223161/39f52877601b/ao4c02234_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a83b/11223161/903dd289178b/ao4c02234_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a83b/11223161/4c61678cacdf/ao4c02234_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a83b/11223161/2f96a4a55503/ao4c02234_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a83b/11223161/39f52877601b/ao4c02234_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a83b/11223161/903dd289178b/ao4c02234_0004.jpg

相似文献

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Enhancing Therapeutic Efficacy in Cancer Treatment: Integrating Nanomedicine with Autophagy Inhibition Strategies.

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[1]
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[2]
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[3]
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[4]
Revolutionizing Cancer Immunotherapy: Emerging Nanotechnology-Driven Drug Delivery Systems for Enhanced Therapeutic Efficacy.

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[5]
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本文引用的文献

[1]
Correction to: Nanomedicine for autophagy modulation in cancer therapy: a clinical perspective.

Cell Biosci. 2023-6-9

[2]
Drug-induced self-assembled nanovesicles for doxorubicin resistance reversal via autophagy inhibition and delivery synchronism.

Theranostics. 2022

[3]
Co-delivery of doxorubicin and shRNA of Beclin1 by folate receptor targeted pullulan-based multifunctional nanomicelles for combinational cancer therapy.

RSC Adv. 2018-5-15

[4]
Targeted Codelivery of Docetaxel and Atg7 siRNA for Autophagy Inhibition and Pancreatic Cancer Treatment.

ACS Appl Bio Mater. 2019-3-18

[5]
Co-delivery of the autophagy inhibitor si-Beclin1 and the doxorubicin nano-delivery system for advanced prostate cancer treatment.

J Biomater Appl. 2022-2

[6]
MicroRNA miR-30a inhibits cisplatin resistance in ovarian cancer cells through autophagy.

Bioengineered. 2021-12

[7]
Enhanced Cancer Starvation Therapy Based on Glucose Oxidase/3-Methyladenine-Loaded Dendritic Mesoporous OrganoSilicon Nanoparticles.

Biomolecules. 2021-9-14

[8]
miR-30a-5p suppresses lung squamous cell carcinoma via ATG5 - mediated autophagy.

Aging (Albany NY). 2021-7-12

[9]
MicroRNA-373-3p inhibits the growth of cervical cancer by targeting AKT1 both in vitro and in vivo.

Acta Biochim Pol. 2021-7-8

[10]
Rhaponticin suppresses osteosarcoma through the inhibition of PI3K-Akt-mTOR pathway.

Saudi J Biol Sci. 2021-7

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