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Targeting lncRNAs in programmed cell death as a therapeutic strategy for non-small cell lung cancer
Lung cancer is a leading cause of cancer-related mortality worldwide, with non-small cell lung cancer (NSCLC) being the most common histological type. Owing to the limited therapeutic efficacy and side effects of currently available therapies for NSCLC, it is necessary to identify novel therapeutic...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8980082/ https://www.ncbi.nlm.nih.gov/pubmed/35379783 http://dx.doi.org/10.1038/s41420-022-00982-x |
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author | Luo, Yanqin Li, Jingyang Yu, Peng Sun, Jiayi Hu, Yingfan Meng, Xianli Xiang, Li |
author_facet | Luo, Yanqin Li, Jingyang Yu, Peng Sun, Jiayi Hu, Yingfan Meng, Xianli Xiang, Li |
author_sort | Luo, Yanqin |
collection | PubMed |
description | Lung cancer is a leading cause of cancer-related mortality worldwide, with non-small cell lung cancer (NSCLC) being the most common histological type. Owing to the limited therapeutic efficacy and side effects of currently available therapies for NSCLC, it is necessary to identify novel therapeutic targets for NSCLC. Long non-coding RNAs (lncRNAs) are non-protein-coding RNAs with a transcript length of more than 200 nucleotides, which play a vital role in the tumorigenesis and progression of multiple cancers, including NSCLC. Induction of programmed cell death (PCD) is the main mechanism leading to tumour cell death in most cancer treatments. Recent studies have demonstrated that lncRNAs are closely correlated with PCD including apoptosis, pyroptosis, autophagy and ferroptosis, which can regulate PCD and relevant death pathways to affect NSCLC progression and the efficacy of clinical therapy. Therefore, in this review, we focused on the function of lncRNAs in PCD of NSCLC and summarized the therapeutic role of targeting lncRNAs in PCD for NSCLC treatment, aiming to provide new sights into the underlying pathogenic mechanisms and propose a potential new strategy for NSCLC therapy so as to improve therapeutic outcomes with the ultimate goal to benefit the patients. |
format | Online Article Text |
id | pubmed-8980082 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-89800822022-04-20 Targeting lncRNAs in programmed cell death as a therapeutic strategy for non-small cell lung cancer Luo, Yanqin Li, Jingyang Yu, Peng Sun, Jiayi Hu, Yingfan Meng, Xianli Xiang, Li Cell Death Discov Review Article Lung cancer is a leading cause of cancer-related mortality worldwide, with non-small cell lung cancer (NSCLC) being the most common histological type. Owing to the limited therapeutic efficacy and side effects of currently available therapies for NSCLC, it is necessary to identify novel therapeutic targets for NSCLC. Long non-coding RNAs (lncRNAs) are non-protein-coding RNAs with a transcript length of more than 200 nucleotides, which play a vital role in the tumorigenesis and progression of multiple cancers, including NSCLC. Induction of programmed cell death (PCD) is the main mechanism leading to tumour cell death in most cancer treatments. Recent studies have demonstrated that lncRNAs are closely correlated with PCD including apoptosis, pyroptosis, autophagy and ferroptosis, which can regulate PCD and relevant death pathways to affect NSCLC progression and the efficacy of clinical therapy. Therefore, in this review, we focused on the function of lncRNAs in PCD of NSCLC and summarized the therapeutic role of targeting lncRNAs in PCD for NSCLC treatment, aiming to provide new sights into the underlying pathogenic mechanisms and propose a potential new strategy for NSCLC therapy so as to improve therapeutic outcomes with the ultimate goal to benefit the patients. Nature Publishing Group UK 2022-04-04 /pmc/articles/PMC8980082/ /pubmed/35379783 http://dx.doi.org/10.1038/s41420-022-00982-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Review Article Luo, Yanqin Li, Jingyang Yu, Peng Sun, Jiayi Hu, Yingfan Meng, Xianli Xiang, Li Targeting lncRNAs in programmed cell death as a therapeutic strategy for non-small cell lung cancer |
title | Targeting lncRNAs in programmed cell death as a therapeutic strategy for non-small cell lung cancer |
title_full | Targeting lncRNAs in programmed cell death as a therapeutic strategy for non-small cell lung cancer |
title_fullStr | Targeting lncRNAs in programmed cell death as a therapeutic strategy for non-small cell lung cancer |
title_full_unstemmed | Targeting lncRNAs in programmed cell death as a therapeutic strategy for non-small cell lung cancer |
title_short | Targeting lncRNAs in programmed cell death as a therapeutic strategy for non-small cell lung cancer |
title_sort | targeting lncrnas in programmed cell death as a therapeutic strategy for non-small cell lung cancer |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8980082/ https://www.ncbi.nlm.nih.gov/pubmed/35379783 http://dx.doi.org/10.1038/s41420-022-00982-x |
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