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Identifying MicroRNAs Suitable for Detection of Breast Cancer: A Systematic Review of Discovery Phases Studies on MicroRNA Expression Profiles

The analysis of circulating tumor cells and tumor-derived materials, such as circulating tumor DNA, circulating miRNAs (cfmiRNAs), and extracellular vehicles provides crucial information in cancer research. CfmiRNAs, a group of short noncoding regulatory RNAs, have gained attention as diagnostic and...

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Autores principales: Padroni, Lisa, De Marco, Laura, Fiano, Valentina, Milani, Lorenzo, Marmiroli, Giorgia, Giraudo, Maria Teresa, Macciotta, Alessandra, Ricceri, Fulvio, Sacerdote, Carlotta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10607026/
https://www.ncbi.nlm.nih.gov/pubmed/37894794
http://dx.doi.org/10.3390/ijms242015114
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author Padroni, Lisa
De Marco, Laura
Fiano, Valentina
Milani, Lorenzo
Marmiroli, Giorgia
Giraudo, Maria Teresa
Macciotta, Alessandra
Ricceri, Fulvio
Sacerdote, Carlotta
author_facet Padroni, Lisa
De Marco, Laura
Fiano, Valentina
Milani, Lorenzo
Marmiroli, Giorgia
Giraudo, Maria Teresa
Macciotta, Alessandra
Ricceri, Fulvio
Sacerdote, Carlotta
author_sort Padroni, Lisa
collection PubMed
description The analysis of circulating tumor cells and tumor-derived materials, such as circulating tumor DNA, circulating miRNAs (cfmiRNAs), and extracellular vehicles provides crucial information in cancer research. CfmiRNAs, a group of short noncoding regulatory RNAs, have gained attention as diagnostic and prognostic biomarkers. This review focuses on the discovery phases of cfmiRNA studies in breast cancer patients, aiming to identify altered cfmiRNA levels compared to healthy controls. A systematic literature search was conducted, resulting in 16 eligible publications. The studies included a total of 585 breast cancer cases and 496 healthy controls, with diverse sample types and different cfmiRNA assay panels. Several cfmiRNAs, including MIR16, MIR191, MIR484, MIR106a, and MIR193b, showed differential expressions between breast cancer cases and healthy controls. However, the studies had a high risk of bias and lacked standardized protocols. The findings highlight the need for robust study designs, standardized procedures, and larger sample sizes in discovery phase studies. Furthermore, the identified cfmiRNAs can serve as potential candidates for further validation studies in different populations. Improving the design and implementation of cfmiRNA research in liquid biopsies may enhance their clinical diagnostic utility in breast cancer patients.
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spelling pubmed-106070262023-10-28 Identifying MicroRNAs Suitable for Detection of Breast Cancer: A Systematic Review of Discovery Phases Studies on MicroRNA Expression Profiles Padroni, Lisa De Marco, Laura Fiano, Valentina Milani, Lorenzo Marmiroli, Giorgia Giraudo, Maria Teresa Macciotta, Alessandra Ricceri, Fulvio Sacerdote, Carlotta Int J Mol Sci Review The analysis of circulating tumor cells and tumor-derived materials, such as circulating tumor DNA, circulating miRNAs (cfmiRNAs), and extracellular vehicles provides crucial information in cancer research. CfmiRNAs, a group of short noncoding regulatory RNAs, have gained attention as diagnostic and prognostic biomarkers. This review focuses on the discovery phases of cfmiRNA studies in breast cancer patients, aiming to identify altered cfmiRNA levels compared to healthy controls. A systematic literature search was conducted, resulting in 16 eligible publications. The studies included a total of 585 breast cancer cases and 496 healthy controls, with diverse sample types and different cfmiRNA assay panels. Several cfmiRNAs, including MIR16, MIR191, MIR484, MIR106a, and MIR193b, showed differential expressions between breast cancer cases and healthy controls. However, the studies had a high risk of bias and lacked standardized protocols. The findings highlight the need for robust study designs, standardized procedures, and larger sample sizes in discovery phase studies. Furthermore, the identified cfmiRNAs can serve as potential candidates for further validation studies in different populations. Improving the design and implementation of cfmiRNA research in liquid biopsies may enhance their clinical diagnostic utility in breast cancer patients. MDPI 2023-10-12 /pmc/articles/PMC10607026/ /pubmed/37894794 http://dx.doi.org/10.3390/ijms242015114 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Padroni, Lisa
De Marco, Laura
Fiano, Valentina
Milani, Lorenzo
Marmiroli, Giorgia
Giraudo, Maria Teresa
Macciotta, Alessandra
Ricceri, Fulvio
Sacerdote, Carlotta
Identifying MicroRNAs Suitable for Detection of Breast Cancer: A Systematic Review of Discovery Phases Studies on MicroRNA Expression Profiles
title Identifying MicroRNAs Suitable for Detection of Breast Cancer: A Systematic Review of Discovery Phases Studies on MicroRNA Expression Profiles
title_full Identifying MicroRNAs Suitable for Detection of Breast Cancer: A Systematic Review of Discovery Phases Studies on MicroRNA Expression Profiles
title_fullStr Identifying MicroRNAs Suitable for Detection of Breast Cancer: A Systematic Review of Discovery Phases Studies on MicroRNA Expression Profiles
title_full_unstemmed Identifying MicroRNAs Suitable for Detection of Breast Cancer: A Systematic Review of Discovery Phases Studies on MicroRNA Expression Profiles
title_short Identifying MicroRNAs Suitable for Detection of Breast Cancer: A Systematic Review of Discovery Phases Studies on MicroRNA Expression Profiles
title_sort identifying micrornas suitable for detection of breast cancer: a systematic review of discovery phases studies on microrna expression profiles
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10607026/
https://www.ncbi.nlm.nih.gov/pubmed/37894794
http://dx.doi.org/10.3390/ijms242015114
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