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The expression profile of RNA sensors in colorectal cancer and its correlation with cancer stages

BACKGROUND: RNA sensors represent the most important pattern recognition receptors (PRRs) to defend against RNA pathogens, such as RNA viruses. Recent studies revealed their critical roles in inflammatory and autoimmune diseases. Furthermore, more recent evidences indicated that RNA sensors mediate...

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Autores principales: He, Liangmei, Wang, Fei, Tian, Hongbo, Xie, Yuan, Xie, Lu, Liu, Zhiping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8799165/
https://www.ncbi.nlm.nih.gov/pubmed/35116878
http://dx.doi.org/10.21037/tcr.2019.07.45
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author He, Liangmei
Wang, Fei
Tian, Hongbo
Xie, Yuan
Xie, Lu
Liu, Zhiping
author_facet He, Liangmei
Wang, Fei
Tian, Hongbo
Xie, Yuan
Xie, Lu
Liu, Zhiping
author_sort He, Liangmei
collection PubMed
description BACKGROUND: RNA sensors represent the most important pattern recognition receptors (PRRs) to defend against RNA pathogens, such as RNA viruses. Recent studies revealed their critical roles in inflammatory and autoimmune diseases. Furthermore, more recent evidences indicated that RNA sensors mediate the development of colitis or colorectal cancer (CRC). However, a systematic understanding of RNA sensors in CRC is still lacking, especially the expression patterns in CRC. METHODS: Here, we analyzed RNA sensor expression, clinical significance, and possible mechanisms in CRC by combining bioinformatic analysis and the analysis on pre-cancerous animal model and clinical tissue samples. RESULTS: We found that most of the members of RNA sensors, including RNA-sensing Toll-like receptors (TLR3, TLR7, and TLR8) and RIG-I-like receptors (MDA5 and RIG-I), were down-regulated in CRC, while the expression of DDX21 were up-regulated in human CRC. In addition, we also analyzed the correlation between gene expression and cancer stages. We found that the expression of RNA-sensing TLRs, RIG-I, and DDX21 in CRC were associated with cancer stages. Finally, in order to explore the possible mechanisms, the correlation between RNA sensors and the main downstream signaling molecules were analyzed. A positive correlation was observed in TLR7/8 and MyD88, RIG-I/MDA5 and LGP2, while a negative correlation was observed in RIG-I/MDA5 and MAVS. CONCLUSIONS: This study reveals the potential values of RNA-sensing genes including TLRs, RIG-I and DDX21 as biomarkers of CRC formation, progression and therapy.
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spelling pubmed-87991652022-02-02 The expression profile of RNA sensors in colorectal cancer and its correlation with cancer stages He, Liangmei Wang, Fei Tian, Hongbo Xie, Yuan Xie, Lu Liu, Zhiping Transl Cancer Res Original Article BACKGROUND: RNA sensors represent the most important pattern recognition receptors (PRRs) to defend against RNA pathogens, such as RNA viruses. Recent studies revealed their critical roles in inflammatory and autoimmune diseases. Furthermore, more recent evidences indicated that RNA sensors mediate the development of colitis or colorectal cancer (CRC). However, a systematic understanding of RNA sensors in CRC is still lacking, especially the expression patterns in CRC. METHODS: Here, we analyzed RNA sensor expression, clinical significance, and possible mechanisms in CRC by combining bioinformatic analysis and the analysis on pre-cancerous animal model and clinical tissue samples. RESULTS: We found that most of the members of RNA sensors, including RNA-sensing Toll-like receptors (TLR3, TLR7, and TLR8) and RIG-I-like receptors (MDA5 and RIG-I), were down-regulated in CRC, while the expression of DDX21 were up-regulated in human CRC. In addition, we also analyzed the correlation between gene expression and cancer stages. We found that the expression of RNA-sensing TLRs, RIG-I, and DDX21 in CRC were associated with cancer stages. Finally, in order to explore the possible mechanisms, the correlation between RNA sensors and the main downstream signaling molecules were analyzed. A positive correlation was observed in TLR7/8 and MyD88, RIG-I/MDA5 and LGP2, while a negative correlation was observed in RIG-I/MDA5 and MAVS. CONCLUSIONS: This study reveals the potential values of RNA-sensing genes including TLRs, RIG-I and DDX21 as biomarkers of CRC formation, progression and therapy. AME Publishing Company 2019-08 /pmc/articles/PMC8799165/ /pubmed/35116878 http://dx.doi.org/10.21037/tcr.2019.07.45 Text en 2019 Translational Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.
spellingShingle Original Article
He, Liangmei
Wang, Fei
Tian, Hongbo
Xie, Yuan
Xie, Lu
Liu, Zhiping
The expression profile of RNA sensors in colorectal cancer and its correlation with cancer stages
title The expression profile of RNA sensors in colorectal cancer and its correlation with cancer stages
title_full The expression profile of RNA sensors in colorectal cancer and its correlation with cancer stages
title_fullStr The expression profile of RNA sensors in colorectal cancer and its correlation with cancer stages
title_full_unstemmed The expression profile of RNA sensors in colorectal cancer and its correlation with cancer stages
title_short The expression profile of RNA sensors in colorectal cancer and its correlation with cancer stages
title_sort expression profile of rna sensors in colorectal cancer and its correlation with cancer stages
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8799165/
https://www.ncbi.nlm.nih.gov/pubmed/35116878
http://dx.doi.org/10.21037/tcr.2019.07.45
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