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MiRNA-93: a novel signature in human disorders and drug resistance
miRNA-93 is a member of the miR-106b-25 family and is encoded by a gene on chromosome 7q22.1. They play a role in the etiology of various diseases, including cancer, Parkinson’s disease, hepatic injury, osteoarthritis, acute myocardial infarction, atherosclerosis, rheumatoid arthritis, and chronic k...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10114484/ https://www.ncbi.nlm.nih.gov/pubmed/37076893 http://dx.doi.org/10.1186/s12964-023-01106-3 |
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author | Hussen, Bashdar Mahmud Abdullah, Snur Rasool Rasul, Mohammed Fatih Jawhar, Zanko Hassan Faraj, Goran Sedeeq Hama Kiani, Arda Taheri, Mohammad |
author_facet | Hussen, Bashdar Mahmud Abdullah, Snur Rasool Rasul, Mohammed Fatih Jawhar, Zanko Hassan Faraj, Goran Sedeeq Hama Kiani, Arda Taheri, Mohammad |
author_sort | Hussen, Bashdar Mahmud |
collection | PubMed |
description | miRNA-93 is a member of the miR-106b-25 family and is encoded by a gene on chromosome 7q22.1. They play a role in the etiology of various diseases, including cancer, Parkinson’s disease, hepatic injury, osteoarthritis, acute myocardial infarction, atherosclerosis, rheumatoid arthritis, and chronic kidney disease. Different studies have found that this miRNA has opposing roles in the context of cancer. Recently, miRNA-93 has been downregulated in breast cancer, gastric cancer, colorectal cancer, pancreatic cancer, bladder cancer, cervical cancer, and renal cancer. However, miRNA-93 is up-regulated in a wide variety of malignancies, such as lung, colorectal, glioma, prostate, osteosarcoma, and hepatocellular carcinoma. The aim of the current review is to provide an overview of miRNA-93's function in cancer disorder progression and non-cancer disorders, with a focus on dysregulated signaling pathways. We also give an overview of this miRNA's function as a biomarker of prognosis in cancer and emphasize how it contributes to drug resistance based on in vivo, in vitro, and human studies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12964-023-01106-3. |
format | Online Article Text |
id | pubmed-10114484 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-101144842023-04-20 MiRNA-93: a novel signature in human disorders and drug resistance Hussen, Bashdar Mahmud Abdullah, Snur Rasool Rasul, Mohammed Fatih Jawhar, Zanko Hassan Faraj, Goran Sedeeq Hama Kiani, Arda Taheri, Mohammad Cell Commun Signal Review miRNA-93 is a member of the miR-106b-25 family and is encoded by a gene on chromosome 7q22.1. They play a role in the etiology of various diseases, including cancer, Parkinson’s disease, hepatic injury, osteoarthritis, acute myocardial infarction, atherosclerosis, rheumatoid arthritis, and chronic kidney disease. Different studies have found that this miRNA has opposing roles in the context of cancer. Recently, miRNA-93 has been downregulated in breast cancer, gastric cancer, colorectal cancer, pancreatic cancer, bladder cancer, cervical cancer, and renal cancer. However, miRNA-93 is up-regulated in a wide variety of malignancies, such as lung, colorectal, glioma, prostate, osteosarcoma, and hepatocellular carcinoma. The aim of the current review is to provide an overview of miRNA-93's function in cancer disorder progression and non-cancer disorders, with a focus on dysregulated signaling pathways. We also give an overview of this miRNA's function as a biomarker of prognosis in cancer and emphasize how it contributes to drug resistance based on in vivo, in vitro, and human studies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12964-023-01106-3. BioMed Central 2023-04-19 /pmc/articles/PMC10114484/ /pubmed/37076893 http://dx.doi.org/10.1186/s12964-023-01106-3 Text en © The Author(s) 2023 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review Hussen, Bashdar Mahmud Abdullah, Snur Rasool Rasul, Mohammed Fatih Jawhar, Zanko Hassan Faraj, Goran Sedeeq Hama Kiani, Arda Taheri, Mohammad MiRNA-93: a novel signature in human disorders and drug resistance |
title | MiRNA-93: a novel signature in human disorders and drug resistance |
title_full | MiRNA-93: a novel signature in human disorders and drug resistance |
title_fullStr | MiRNA-93: a novel signature in human disorders and drug resistance |
title_full_unstemmed | MiRNA-93: a novel signature in human disorders and drug resistance |
title_short | MiRNA-93: a novel signature in human disorders and drug resistance |
title_sort | mirna-93: a novel signature in human disorders and drug resistance |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10114484/ https://www.ncbi.nlm.nih.gov/pubmed/37076893 http://dx.doi.org/10.1186/s12964-023-01106-3 |
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