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Circulating microRNA profiles in Wilms tumour (WT): A systematic review and meta-analysis of diagnostic test accuracy

BACKGROUND: Wilms tumour (WT) is caused by aberrant embryonic kidney development and associated with dysregulated expression of short, non-protein-coding RNAs termed microRNAs (miRNAs). At present, there is no reliable circulating biomarker of WT, and this remains an urgent unmet clinical need. Such...

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Autores principales: Benlhachemi, Sara, Abouqal, Redouane, Coleman, Nicholas, Murray, Matthew Jonathan, Khattab, Mohammed, El fahime, Elmostafa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: KeAi Publishing 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10247954/
https://www.ncbi.nlm.nih.gov/pubmed/37305178
http://dx.doi.org/10.1016/j.ncrna.2023.05.007
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author Benlhachemi, Sara
Abouqal, Redouane
Coleman, Nicholas
Murray, Matthew Jonathan
Khattab, Mohammed
El fahime, Elmostafa
author_facet Benlhachemi, Sara
Abouqal, Redouane
Coleman, Nicholas
Murray, Matthew Jonathan
Khattab, Mohammed
El fahime, Elmostafa
author_sort Benlhachemi, Sara
collection PubMed
description BACKGROUND: Wilms tumour (WT) is caused by aberrant embryonic kidney development and associated with dysregulated expression of short, non-protein-coding RNAs termed microRNAs (miRNAs). At present, there is no reliable circulating biomarker of WT, and this remains an urgent unmet clinical need. Such biomarkers may assist diagnosis, subtyping/prognostication, and disease-monitoring. Here, we established the list of dysregulated circulating miRNAs in WT from the existing published literature. METHODS: Regardless of publication date, PubMed, Scopus, Web-of-Science, and Wiley online library databases were searched for English/French studies on WT circulating miRNAs. The PRISMA-compliant search was registered in PROSPERO. The QUADAS tool measured retained article quality. The meta-analysis assessed the sensitivity and specificity of miRNAs for WT diagnosis. RESULTS: Qualitative analysis included 280 samples (172 WT patients; 108 healthy controls) from five of 450 published articles. The study uncovered 301 dysregulated miRNAs (144 up-regulated, 143 down-regulated, 14 conflicting). The pooled sensitivity, specificity, and AUC of the 49 significantly dysregulated microRNAs from two studies was 0.67 [0.62; 0.73], 0.95 [0.92; 0.96] and 0.77 [0.73; 0.81] respectively, indicating a stronger diagnostic potential for WT. CONCLUSIONS: Circulating miRNAs show promise for WT diagnosis and prognosis. More research is needed to confirm these findings and determine associations with tumour stage/subtype. PROSPERO REGISTRATION NUMBER: CRD42022301597.
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spelling pubmed-102479542023-06-09 Circulating microRNA profiles in Wilms tumour (WT): A systematic review and meta-analysis of diagnostic test accuracy Benlhachemi, Sara Abouqal, Redouane Coleman, Nicholas Murray, Matthew Jonathan Khattab, Mohammed El fahime, Elmostafa Noncoding RNA Res Article BACKGROUND: Wilms tumour (WT) is caused by aberrant embryonic kidney development and associated with dysregulated expression of short, non-protein-coding RNAs termed microRNAs (miRNAs). At present, there is no reliable circulating biomarker of WT, and this remains an urgent unmet clinical need. Such biomarkers may assist diagnosis, subtyping/prognostication, and disease-monitoring. Here, we established the list of dysregulated circulating miRNAs in WT from the existing published literature. METHODS: Regardless of publication date, PubMed, Scopus, Web-of-Science, and Wiley online library databases were searched for English/French studies on WT circulating miRNAs. The PRISMA-compliant search was registered in PROSPERO. The QUADAS tool measured retained article quality. The meta-analysis assessed the sensitivity and specificity of miRNAs for WT diagnosis. RESULTS: Qualitative analysis included 280 samples (172 WT patients; 108 healthy controls) from five of 450 published articles. The study uncovered 301 dysregulated miRNAs (144 up-regulated, 143 down-regulated, 14 conflicting). The pooled sensitivity, specificity, and AUC of the 49 significantly dysregulated microRNAs from two studies was 0.67 [0.62; 0.73], 0.95 [0.92; 0.96] and 0.77 [0.73; 0.81] respectively, indicating a stronger diagnostic potential for WT. CONCLUSIONS: Circulating miRNAs show promise for WT diagnosis and prognosis. More research is needed to confirm these findings and determine associations with tumour stage/subtype. PROSPERO REGISTRATION NUMBER: CRD42022301597. KeAi Publishing 2023-05-26 /pmc/articles/PMC10247954/ /pubmed/37305178 http://dx.doi.org/10.1016/j.ncrna.2023.05.007 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Benlhachemi, Sara
Abouqal, Redouane
Coleman, Nicholas
Murray, Matthew Jonathan
Khattab, Mohammed
El fahime, Elmostafa
Circulating microRNA profiles in Wilms tumour (WT): A systematic review and meta-analysis of diagnostic test accuracy
title Circulating microRNA profiles in Wilms tumour (WT): A systematic review and meta-analysis of diagnostic test accuracy
title_full Circulating microRNA profiles in Wilms tumour (WT): A systematic review and meta-analysis of diagnostic test accuracy
title_fullStr Circulating microRNA profiles in Wilms tumour (WT): A systematic review and meta-analysis of diagnostic test accuracy
title_full_unstemmed Circulating microRNA profiles in Wilms tumour (WT): A systematic review and meta-analysis of diagnostic test accuracy
title_short Circulating microRNA profiles in Wilms tumour (WT): A systematic review and meta-analysis of diagnostic test accuracy
title_sort circulating microrna profiles in wilms tumour (wt): a systematic review and meta-analysis of diagnostic test accuracy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10247954/
https://www.ncbi.nlm.nih.gov/pubmed/37305178
http://dx.doi.org/10.1016/j.ncrna.2023.05.007
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