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Revisiting cancer hallmarks: insights from the interplay between oxidative stress and non-coding RNAs

Cancer is one of the most common disease worldwide, with complex changes and certain traits which have been described as “The Hallmarks of Cancer.” Despite increasing studies on in-depth investigation of these hallmarks, the molecular mechanisms associated with tumorigenesis have still not yet been...

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Autores principales: Zhou, Li, Zhang, Zhe, Huang, Zhao, Nice, Edouard, Zou, Bingwen, Huang, Canhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Singapore 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8603983/
https://www.ncbi.nlm.nih.gov/pubmed/35006436
http://dx.doi.org/10.1186/s43556-020-00004-1
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author Zhou, Li
Zhang, Zhe
Huang, Zhao
Nice, Edouard
Zou, Bingwen
Huang, Canhua
author_facet Zhou, Li
Zhang, Zhe
Huang, Zhao
Nice, Edouard
Zou, Bingwen
Huang, Canhua
author_sort Zhou, Li
collection PubMed
description Cancer is one of the most common disease worldwide, with complex changes and certain traits which have been described as “The Hallmarks of Cancer.” Despite increasing studies on in-depth investigation of these hallmarks, the molecular mechanisms associated with tumorigenesis have still not yet been fully defined. Recently, accumulating evidence supports the observation that microRNAs and long noncoding RNAs (lncRNAs), two main classes of noncoding RNAs (ncRNAs), regulate most cancer hallmarks through their binding with DNA, RNA or proteins, or encoding small peptides. Reactive oxygen species (ROS), the byproducts generated during metabolic processes, are known to regulate every step of tumorigenesis by acting as second messengers in cancer cells. The disturbance in ROS homeostasis leads to a specific pathological state termed “oxidative stress”, which plays essential roles in regulation of cancer progression. In addition, the interplay between oxidative stress and ncRNAs is found to regulate the expression of multiple genes and the activation of several signaling pathways involved in cancer hallmarks, revealing a potential mechanistic relationship involving ncRNAs, oxidative stress and cancer. In this review, we provide evidence that shows the essential role of ncRNAs and the interplay between oxidative stress and ncRNAs in regulating cancer hallmarks, which may expand our understanding of ncRNAs in the cancer development from the new perspective.
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spelling pubmed-86039832021-12-01 Revisiting cancer hallmarks: insights from the interplay between oxidative stress and non-coding RNAs Zhou, Li Zhang, Zhe Huang, Zhao Nice, Edouard Zou, Bingwen Huang, Canhua Mol Biomed Review Cancer is one of the most common disease worldwide, with complex changes and certain traits which have been described as “The Hallmarks of Cancer.” Despite increasing studies on in-depth investigation of these hallmarks, the molecular mechanisms associated with tumorigenesis have still not yet been fully defined. Recently, accumulating evidence supports the observation that microRNAs and long noncoding RNAs (lncRNAs), two main classes of noncoding RNAs (ncRNAs), regulate most cancer hallmarks through their binding with DNA, RNA or proteins, or encoding small peptides. Reactive oxygen species (ROS), the byproducts generated during metabolic processes, are known to regulate every step of tumorigenesis by acting as second messengers in cancer cells. The disturbance in ROS homeostasis leads to a specific pathological state termed “oxidative stress”, which plays essential roles in regulation of cancer progression. In addition, the interplay between oxidative stress and ncRNAs is found to regulate the expression of multiple genes and the activation of several signaling pathways involved in cancer hallmarks, revealing a potential mechanistic relationship involving ncRNAs, oxidative stress and cancer. In this review, we provide evidence that shows the essential role of ncRNAs and the interplay between oxidative stress and ncRNAs in regulating cancer hallmarks, which may expand our understanding of ncRNAs in the cancer development from the new perspective. Springer Singapore 2020-08-31 /pmc/articles/PMC8603983/ /pubmed/35006436 http://dx.doi.org/10.1186/s43556-020-00004-1 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Review
Zhou, Li
Zhang, Zhe
Huang, Zhao
Nice, Edouard
Zou, Bingwen
Huang, Canhua
Revisiting cancer hallmarks: insights from the interplay between oxidative stress and non-coding RNAs
title Revisiting cancer hallmarks: insights from the interplay between oxidative stress and non-coding RNAs
title_full Revisiting cancer hallmarks: insights from the interplay between oxidative stress and non-coding RNAs
title_fullStr Revisiting cancer hallmarks: insights from the interplay between oxidative stress and non-coding RNAs
title_full_unstemmed Revisiting cancer hallmarks: insights from the interplay between oxidative stress and non-coding RNAs
title_short Revisiting cancer hallmarks: insights from the interplay between oxidative stress and non-coding RNAs
title_sort revisiting cancer hallmarks: insights from the interplay between oxidative stress and non-coding rnas
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8603983/
https://www.ncbi.nlm.nih.gov/pubmed/35006436
http://dx.doi.org/10.1186/s43556-020-00004-1
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