Targeting non-coding RNAs to overcome cancer therapy resistance

Abstract It is now well known that non-coding RNAs (ncRNAs), rather than protein-coding transcripts, are the preponderant RNA transcripts. NcRNAs, particularly microRNAs (miRNAs), long non-coding RNAs (lncRNAs), and circular RNAs (circRNAs), are widely appreciated as pervasive regulators of multiple...

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Main Authors: BaoQing Chen, Mihnea P. Dragomir, Chen Yang, Qiaoqiao Li, David Horst, George A. Calin
Format: Article
Language:English
Published: Nature Publishing Group 2022-04-01
Series:Signal Transduction and Targeted Therapy
Online Access:https://doi.org/10.1038/s41392-022-00975-3
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author BaoQing Chen
Mihnea P. Dragomir
Chen Yang
Qiaoqiao Li
David Horst
George A. Calin
author_facet BaoQing Chen
Mihnea P. Dragomir
Chen Yang
Qiaoqiao Li
David Horst
George A. Calin
author_sort BaoQing Chen
collection DOAJ
description Abstract It is now well known that non-coding RNAs (ncRNAs), rather than protein-coding transcripts, are the preponderant RNA transcripts. NcRNAs, particularly microRNAs (miRNAs), long non-coding RNAs (lncRNAs), and circular RNAs (circRNAs), are widely appreciated as pervasive regulators of multiple cancer hallmarks such as proliferation, apoptosis, invasion, metastasis, and genomic instability. Despite recent discoveries in cancer therapy, resistance to chemotherapy, radiotherapy, targeted therapy, and immunotherapy continue to be a major setback. Recent studies have shown that ncRNAs also play a major role in resistance to different cancer therapies by rewiring essential signaling pathways. In this review, we present the intricate mechanisms through which dysregulated ncRNAs control resistance to the four major types of cancer therapies. We will focus on the current clinical implications of ncRNAs as biomarkers to predict treatment response (intrinsic resistance) and to detect resistance to therapy after the start of treatment (acquired resistance). Furthermore, we will present the potential of targeting ncRNA to overcome cancer treatment resistance, and we will discuss the challenges of ncRNA-targeted therapy—especially the development of delivery systems.
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spelling doaj.art-f53841bc61ce490b838c6002f740738c2022-12-22T01:51:57ZengNature Publishing GroupSignal Transduction and Targeted Therapy2059-36352022-04-017112010.1038/s41392-022-00975-3Targeting non-coding RNAs to overcome cancer therapy resistanceBaoQing Chen0Mihnea P. Dragomir1Chen Yang2Qiaoqiao Li3David Horst4George A. Calin5Department of Radiation Oncology, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University Cancer Center, GuangzhouInstitute of Pathology, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin and Berlin Institute of HealthDepartment of Radiation Oncology, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University Cancer Center, GuangzhouDepartment of Radiation Oncology, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University Cancer Center, GuangzhouInstitute of Pathology, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin and Berlin Institute of HealthDepartment of Translational Molecular Pathology, The University of Texas MD Anderson Cancer CenterAbstract It is now well known that non-coding RNAs (ncRNAs), rather than protein-coding transcripts, are the preponderant RNA transcripts. NcRNAs, particularly microRNAs (miRNAs), long non-coding RNAs (lncRNAs), and circular RNAs (circRNAs), are widely appreciated as pervasive regulators of multiple cancer hallmarks such as proliferation, apoptosis, invasion, metastasis, and genomic instability. Despite recent discoveries in cancer therapy, resistance to chemotherapy, radiotherapy, targeted therapy, and immunotherapy continue to be a major setback. Recent studies have shown that ncRNAs also play a major role in resistance to different cancer therapies by rewiring essential signaling pathways. In this review, we present the intricate mechanisms through which dysregulated ncRNAs control resistance to the four major types of cancer therapies. We will focus on the current clinical implications of ncRNAs as biomarkers to predict treatment response (intrinsic resistance) and to detect resistance to therapy after the start of treatment (acquired resistance). Furthermore, we will present the potential of targeting ncRNA to overcome cancer treatment resistance, and we will discuss the challenges of ncRNA-targeted therapy—especially the development of delivery systems.https://doi.org/10.1038/s41392-022-00975-3
spellingShingle BaoQing Chen
Mihnea P. Dragomir
Chen Yang
Qiaoqiao Li
David Horst
George A. Calin
Targeting non-coding RNAs to overcome cancer therapy resistance
Signal Transduction and Targeted Therapy
title Targeting non-coding RNAs to overcome cancer therapy resistance
title_full Targeting non-coding RNAs to overcome cancer therapy resistance
title_fullStr Targeting non-coding RNAs to overcome cancer therapy resistance
title_full_unstemmed Targeting non-coding RNAs to overcome cancer therapy resistance
title_short Targeting non-coding RNAs to overcome cancer therapy resistance
title_sort targeting non coding rnas to overcome cancer therapy resistance
url https://doi.org/10.1038/s41392-022-00975-3
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