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The role of inflammatory miRNA–mRNA interactions in PBMCs of colorectal cancer and obesity patients

INTRODUCTION: Inflammation is a critical hallmark in obesity and colorectal cancer (CRC). This study aimed to investigate effective microRNA (miRNA)–messenger RNA (mRNA) interactions on inflammatory networks involved in obesity and CRC. METHODS: The literature searches were applied to identify genes...

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Autores principales: Gholami, Morteza, Zoughi, Marziyeh, Larijani, Bagher, Abdollahzadeh, Rasoul, Taslimi, Reza, Rahmani, Zeinab, Kazemeini, Alireza, Behboo, Roobic, Razi, Farideh, Bastami, Milad, Hasani‐Ranjbar, Shirin, Amoli, Mahsa M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9609448/
https://www.ncbi.nlm.nih.gov/pubmed/36301024
http://dx.doi.org/10.1002/iid3.702
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author Gholami, Morteza
Zoughi, Marziyeh
Larijani, Bagher
Abdollahzadeh, Rasoul
Taslimi, Reza
Rahmani, Zeinab
Kazemeini, Alireza
Behboo, Roobic
Razi, Farideh
Bastami, Milad
Hasani‐Ranjbar, Shirin
Amoli, Mahsa M.
author_facet Gholami, Morteza
Zoughi, Marziyeh
Larijani, Bagher
Abdollahzadeh, Rasoul
Taslimi, Reza
Rahmani, Zeinab
Kazemeini, Alireza
Behboo, Roobic
Razi, Farideh
Bastami, Milad
Hasani‐Ranjbar, Shirin
Amoli, Mahsa M.
author_sort Gholami, Morteza
collection PubMed
description INTRODUCTION: Inflammation is a critical hallmark in obesity and colorectal cancer (CRC). This study aimed to investigate effective microRNA (miRNA)–messenger RNA (mRNA) interactions on inflammatory networks involved in obesity and CRC. METHODS: The literature searches were applied to identify genes expression reported on peripheral blood mononuclear cells (PBMCs) and/or blood of CRC subjects and to find inflammatory miRNA  in blood samples. Furthermore, bioinformatics analysis was utilized to find inflammatory miRNA:mRNA interactions of the genes. Finally, a case‐control study was set to investigate the expression of LAMC1 and GNB3 genes besides miR‐10b, miR‐506‐3p, miR‐150‐5p, and miR‐124‐3p in CRC and control subjects. RESULTS: The expression of LAMC1 gene in healthy control groups was associated with body mass index (BMI) (p < .05). The level of miR‐10b (p < .001), miR‐506 (p < .001), and miR‐124 (p <. 001) were significantly increased in PBMCs of CRC patients, while they were not associated with BMI. The level of miR‐150 was associated with BMI in healthy subjects (p < .05). CONCLUSIONS: The changes in the level of miR‐506 and miR‐124 in CRC patients may be associated with the regulatory role of these miRNAs on LAMC1 expression. The LAMC1 may be related to BMI, however, more observational studies on other populations are needed.
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spelling pubmed-96094482022-10-28 The role of inflammatory miRNA–mRNA interactions in PBMCs of colorectal cancer and obesity patients Gholami, Morteza Zoughi, Marziyeh Larijani, Bagher Abdollahzadeh, Rasoul Taslimi, Reza Rahmani, Zeinab Kazemeini, Alireza Behboo, Roobic Razi, Farideh Bastami, Milad Hasani‐Ranjbar, Shirin Amoli, Mahsa M. Immun Inflamm Dis Original Articles INTRODUCTION: Inflammation is a critical hallmark in obesity and colorectal cancer (CRC). This study aimed to investigate effective microRNA (miRNA)–messenger RNA (mRNA) interactions on inflammatory networks involved in obesity and CRC. METHODS: The literature searches were applied to identify genes expression reported on peripheral blood mononuclear cells (PBMCs) and/or blood of CRC subjects and to find inflammatory miRNA  in blood samples. Furthermore, bioinformatics analysis was utilized to find inflammatory miRNA:mRNA interactions of the genes. Finally, a case‐control study was set to investigate the expression of LAMC1 and GNB3 genes besides miR‐10b, miR‐506‐3p, miR‐150‐5p, and miR‐124‐3p in CRC and control subjects. RESULTS: The expression of LAMC1 gene in healthy control groups was associated with body mass index (BMI) (p < .05). The level of miR‐10b (p < .001), miR‐506 (p < .001), and miR‐124 (p <. 001) were significantly increased in PBMCs of CRC patients, while they were not associated with BMI. The level of miR‐150 was associated with BMI in healthy subjects (p < .05). CONCLUSIONS: The changes in the level of miR‐506 and miR‐124 in CRC patients may be associated with the regulatory role of these miRNAs on LAMC1 expression. The LAMC1 may be related to BMI, however, more observational studies on other populations are needed. John Wiley and Sons Inc. 2022-10-27 /pmc/articles/PMC9609448/ /pubmed/36301024 http://dx.doi.org/10.1002/iid3.702 Text en © 2022 The Authors. Immunity, Inflammation and Disease published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Gholami, Morteza
Zoughi, Marziyeh
Larijani, Bagher
Abdollahzadeh, Rasoul
Taslimi, Reza
Rahmani, Zeinab
Kazemeini, Alireza
Behboo, Roobic
Razi, Farideh
Bastami, Milad
Hasani‐Ranjbar, Shirin
Amoli, Mahsa M.
The role of inflammatory miRNA–mRNA interactions in PBMCs of colorectal cancer and obesity patients
title The role of inflammatory miRNA–mRNA interactions in PBMCs of colorectal cancer and obesity patients
title_full The role of inflammatory miRNA–mRNA interactions in PBMCs of colorectal cancer and obesity patients
title_fullStr The role of inflammatory miRNA–mRNA interactions in PBMCs of colorectal cancer and obesity patients
title_full_unstemmed The role of inflammatory miRNA–mRNA interactions in PBMCs of colorectal cancer and obesity patients
title_short The role of inflammatory miRNA–mRNA interactions in PBMCs of colorectal cancer and obesity patients
title_sort role of inflammatory mirna–mrna interactions in pbmcs of colorectal cancer and obesity patients
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9609448/
https://www.ncbi.nlm.nih.gov/pubmed/36301024
http://dx.doi.org/10.1002/iid3.702
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