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Advanced approaches of the use of circRNAs as a replacement for cancer therapy.

作者信息

Hama Faraj Goran Sedeeq, Hussen Bashdar Mahmud, Abdullah Snur Rasool, Fatih Rasul Mohammed, Hajiesmaeili Yasaman, Baniahmad Aria, Taheri Mohammad

机构信息

Department of Medical Laboratory Science, Komar University of Science and Technology, Sulaymaniyah, 46001, Iraq.

Department of Biomedical Sciences, College of Science, Cihan University-Erbil, Erbil, Kurdistan Region, 44001, Iraq.

出版信息

Noncoding RNA Res. 2024 Mar 30;9(3):811-830. doi: 10.1016/j.ncrna.2024.03.012. eCollection 2024 Sep.


DOI:10.1016/j.ncrna.2024.03.012
PMID:38590433
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10999493/
Abstract

Cancer is a broad name for a group of diseases in which abnormal cells grow out of control and are characterized by their complexity and recurrence. Although there has been progress in cancer therapy with the entry of precision medicine and immunotherapy, cancer incidence rates have increased globally. Non-coding RNAs in the form of circular RNAs (circRNAs) play crucial roles in the pathogenesis, clinical diagnosis, and therapy of different diseases, including cancer. According to recent studies, circRNAs appear to serve as accurate indicators and therapeutic targets for cancer treatment. However, circRNAs are promising candidates for cutting-edge cancer therapy because of their distinctive circular structure, stability, and wide range of capabilities; many challenges persist that decrease the applications of circRNA-based cancer therapeutics. Here, we explore the roles of circRNAs as a replacement for cancer therapy, highlight the main challenges facing circRNA-based cancer therapies, and discuss the key strategies to overcome these challenges to improve advanced innovative therapies based on circRNAs with long-term health effects.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fae/10999493/2e20766f0caa/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fae/10999493/09a6aee4fd1b/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fae/10999493/d4571c3d6092/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fae/10999493/07266fcfd5e9/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fae/10999493/bd4cdc2f5701/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fae/10999493/e4abbed6e289/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fae/10999493/a3f8cd5015e3/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fae/10999493/48638f89b395/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fae/10999493/2e20766f0caa/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fae/10999493/09a6aee4fd1b/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fae/10999493/d4571c3d6092/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fae/10999493/07266fcfd5e9/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fae/10999493/bd4cdc2f5701/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fae/10999493/e4abbed6e289/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fae/10999493/a3f8cd5015e3/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fae/10999493/48638f89b395/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fae/10999493/2e20766f0caa/gr8.jpg

相似文献

[1]
Advanced approaches of the use of circRNAs as a replacement for cancer therapy.

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引用本文的文献

[1]
Dysfunctional circular RNA network in major depressive disorder: dissecting the cell identity and potential clinical applications.

Mol Psychiatry. 2025-8-22

[2]
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[3]
Circular RNA vaccines: Pioneering the next-gen cancer immunotherapy.

Cancer Pathog Ther. 2024-12-4

[4]
Circular RNAs in cancer.

MedComm (2020). 2025-2-2

[5]
mRNA vaccines as cancer therapies.

Chin Med J (Engl). 2024-12-20

[6]
The role of circRNAs in resistance to doxorubicin.

Cell Commun Signal. 2024-11-29

[7]
Nanoparticles-Delivered Circular RNA Strategy as a Novel Antitumor Approach.

Int J Mol Sci. 2024-8-16

本文引用的文献

[1]
Nanoplatform-Based In Vivo Gene Delivery Systems for Cancer Therapy.

Small. 2024-7

[2]
CircNUP50 is a novel therapeutic target that promotes cisplatin resistance in ovarian cancer by modulating p53 ubiquitination.

J Nanobiotechnology. 2024-1-19

[3]
CircTENM3 inhibites tumor progression via the miR-558/RUNX3 axis in prostate cancer.

J Transl Med. 2023-11-25

[4]
A novel intronic circular RNA circFGFR1 up-regulates FGFR1 by recruiting transcriptional activators P65/FUS and suppressing miR-4687-5p to promote prostate cancer progression.

J Transl Med. 2023-11-22

[5]
m6A-Mediated Biogenesis of circDDIT4 Inhibits Prostate Cancer Progression by Sequestrating ELAVL1/HuR.

Mol Cancer Res. 2023-12-1

[6]
Efficient circular RNA engineering by end-to-end self-targeting and splicing reaction using group I intron ribozyme.

Mol Ther Nucleic Acids. 2023-8-1

[7]
m6A-modified circABCC4 promotes stemness and metastasis of prostate cancer by recruiting IGF2BP2 to increase stability of CCAR1.

Cancer Gene Ther. 2023-10

[8]
CircRNAs in colorectal cancer: potential biomarkers and therapeutic targets.

Cell Death Dis. 2023-6-9

[9]
Circ_0067934 as a novel therapeutic target in cancer: From mechanistic to clinical perspectives.

Pathol Res Pract. 2023-5

[10]
Clinical delivery of circular RNA: Lessons learned from RNA drug development.

Adv Drug Deliv Rev. 2023-6

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