Role of miRNA-145, 148, and 185 and Stem Cells in Prostate Cancer

MicroRNAs (miRNAs) are small non-coding RNA molecules that play a role in cancer linked to the regulation of important cellular processes and pathways involving tumorigenesis, cell proliferation, differentiation, and apoptosis. A lot of human miRNA sequences have been identified which are linked to...

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Main Authors: Donatella Coradduzza, Sara Cruciani, Caterina Arru, Giuseppe Garroni, Aleksei Pashchenko, Mosab Jedea, Silvia Zappavigna, Michele Caraglia, Evzen Amler, Ciriaco Carru, Margherita Maioli
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Language:English
Published: MDPI AG 2022-01-01
Series:International Journal of Molecular Sciences
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Online Access:https://www.mdpi.com/1422-0067/23/3/1626
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author Donatella Coradduzza
Sara Cruciani
Caterina Arru
Giuseppe Garroni
Aleksei Pashchenko
Mosab Jedea
Silvia Zappavigna
Michele Caraglia
Evzen Amler
Ciriaco Carru
Margherita Maioli
author_facet Donatella Coradduzza
Sara Cruciani
Caterina Arru
Giuseppe Garroni
Aleksei Pashchenko
Mosab Jedea
Silvia Zappavigna
Michele Caraglia
Evzen Amler
Ciriaco Carru
Margherita Maioli
author_sort Donatella Coradduzza
collection DOAJ
description MicroRNAs (miRNAs) are small non-coding RNA molecules that play a role in cancer linked to the regulation of important cellular processes and pathways involving tumorigenesis, cell proliferation, differentiation, and apoptosis. A lot of human miRNA sequences have been identified which are linked to cancer pathogenesis. MicroRNAs, in prostate cancer (PC), play a relevant role as biomarkers, show a specific profile, and have been used as therapeutic targets. Prostate cancer (PC) is the most frequently diagnosed cancer in men. Clinical diagnoses among the gold standards for PC diagnosis and monitoring are prostate-specific antigen (PSA) testing, digital rectal examination, and prostate needle biopsies. PSA screening still has a large grey area of patients, which leads to overdiagnosis. Therefore, new biomarkers are needed to improve existing diagnostic tools. The miRNA expression profiles from tumour versus normal tissues are helpful and exhibit significant differences not only between cancerous and non-cancerous tissues, but also between different cancer types and subtypes. In this review, we focus on the role of miRNAs-145, 148, and 185 and their correlation with stem cells in prostate cancer pathogenesis. MiR-145, by modulating multiple oncogenes, regulates different cellular processes in PC, which are involved in the transition from localised to metastatic disease. MiR-148 is downregulated in high-grade tumours, suggesting that the miR-148-3 family might act as tumour suppressors in PC as a potential biomarker for detecting this disease. MiR-185 regulation is still unclear in being able to regulate tumour processes in PC. Nevertheless, other authors confirm the role of this miRNA as a tumour suppressor, suggesting its potential use as a suitable biomarker in disease prognosis. These three miRNAs are all involved in the regulation of prostate cancer stem cell behaviour (PCSCs). Within this contest, PCSCs are often involved in the onset of chemo-resistance in PC, therefore strategies for targeting this subset of cells are strongly required to control the disease. Hence, the relationship between these two players is interesting and important in prostate cancer pathogenesis and in PCSC stemness regulation, in the attempt to pave the way for novel therapeutic targets in prostate cancer.
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spelling doaj.art-10b7044c04a04f42a5572e353076b0ad2023-11-23T16:43:40ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672022-01-01233162610.3390/ijms23031626Role of miRNA-145, 148, and 185 and Stem Cells in Prostate CancerDonatella Coradduzza0Sara Cruciani1Caterina Arru2Giuseppe Garroni3Aleksei Pashchenko4Mosab Jedea5Silvia Zappavigna6Michele Caraglia7Evzen Amler8Ciriaco Carru9Margherita Maioli10Department of Biomedical Sciences, University of Sassari, 07100 Sassari, ItalyDepartment of Biomedical Sciences, University of Sassari, 07100 Sassari, ItalyDepartment of Biomedical Sciences, University of Sassari, 07100 Sassari, ItalyDepartment of Biomedical Sciences, University of Sassari, 07100 Sassari, ItalyDepartment of Biomedical Sciences, University of Sassari, 07100 Sassari, ItalyDepartment of Precision Medicine, University of Campania “L. Vanvitelli”, Via de Crecchio 7, 80138 Naples, ItalyDepartment of Precision Medicine, University of Campania “L. Vanvitelli”, Via de Crecchio 7, 80138 Naples, ItalyDepartment of Precision Medicine, University of Campania “L. Vanvitelli”, Via de Crecchio 7, 80138 Naples, ItalyInstitute of Biophysics, 2nd Faculty of Medicine, Charles University, V Uvalu 84, 150 06 Prague, Czech RepublicDepartment of Biomedical Sciences, University of Sassari, 07100 Sassari, ItalyDepartment of Biomedical Sciences, University of Sassari, 07100 Sassari, ItalyMicroRNAs (miRNAs) are small non-coding RNA molecules that play a role in cancer linked to the regulation of important cellular processes and pathways involving tumorigenesis, cell proliferation, differentiation, and apoptosis. A lot of human miRNA sequences have been identified which are linked to cancer pathogenesis. MicroRNAs, in prostate cancer (PC), play a relevant role as biomarkers, show a specific profile, and have been used as therapeutic targets. Prostate cancer (PC) is the most frequently diagnosed cancer in men. Clinical diagnoses among the gold standards for PC diagnosis and monitoring are prostate-specific antigen (PSA) testing, digital rectal examination, and prostate needle biopsies. PSA screening still has a large grey area of patients, which leads to overdiagnosis. Therefore, new biomarkers are needed to improve existing diagnostic tools. The miRNA expression profiles from tumour versus normal tissues are helpful and exhibit significant differences not only between cancerous and non-cancerous tissues, but also between different cancer types and subtypes. In this review, we focus on the role of miRNAs-145, 148, and 185 and their correlation with stem cells in prostate cancer pathogenesis. MiR-145, by modulating multiple oncogenes, regulates different cellular processes in PC, which are involved in the transition from localised to metastatic disease. MiR-148 is downregulated in high-grade tumours, suggesting that the miR-148-3 family might act as tumour suppressors in PC as a potential biomarker for detecting this disease. MiR-185 regulation is still unclear in being able to regulate tumour processes in PC. Nevertheless, other authors confirm the role of this miRNA as a tumour suppressor, suggesting its potential use as a suitable biomarker in disease prognosis. These three miRNAs are all involved in the regulation of prostate cancer stem cell behaviour (PCSCs). Within this contest, PCSCs are often involved in the onset of chemo-resistance in PC, therefore strategies for targeting this subset of cells are strongly required to control the disease. Hence, the relationship between these two players is interesting and important in prostate cancer pathogenesis and in PCSC stemness regulation, in the attempt to pave the way for novel therapeutic targets in prostate cancer.https://www.mdpi.com/1422-0067/23/3/1626miRNAsstem cellscell proliferationPCSCsprostate cancer
spellingShingle Donatella Coradduzza
Sara Cruciani
Caterina Arru
Giuseppe Garroni
Aleksei Pashchenko
Mosab Jedea
Silvia Zappavigna
Michele Caraglia
Evzen Amler
Ciriaco Carru
Margherita Maioli
Role of miRNA-145, 148, and 185 and Stem Cells in Prostate Cancer
International Journal of Molecular Sciences
miRNAs
stem cells
cell proliferation
PCSCs
prostate cancer
title Role of miRNA-145, 148, and 185 and Stem Cells in Prostate Cancer
title_full Role of miRNA-145, 148, and 185 and Stem Cells in Prostate Cancer
title_fullStr Role of miRNA-145, 148, and 185 and Stem Cells in Prostate Cancer
title_full_unstemmed Role of miRNA-145, 148, and 185 and Stem Cells in Prostate Cancer
title_short Role of miRNA-145, 148, and 185 and Stem Cells in Prostate Cancer
title_sort role of mirna 145 148 and 185 and stem cells in prostate cancer
topic miRNAs
stem cells
cell proliferation
PCSCs
prostate cancer
url https://www.mdpi.com/1422-0067/23/3/1626
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