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Circulating microRNAs as minimal residual disease biomarkers in childhood acute lymphoblastic leukemia

BACKGROUND: Treatment stratification based on bone marrow minimal residual disease (MRD) at set time points has resulted in considerably improved survival in pediatric acute lymphoblastic leukemia (ALL). Treatment response is assessed using bone marrow samples. MicroRNAs (miRs) easily traffic among...

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Autores principales: Rzepiel, Andrea, Kutszegi, Nóra, Gézsi, András, Sági, Judit C., Egyed, Bálint, Péter, György, Butz, Henriett, Nyírő, Gábor, Müller, Judit, Kovács, Gábor T., Szalai, Csaba, Semsei, Ágnes F., Erdélyi, Dániel J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6854698/
https://www.ncbi.nlm.nih.gov/pubmed/31727091
http://dx.doi.org/10.1186/s12967-019-2114-x
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author Rzepiel, Andrea
Kutszegi, Nóra
Gézsi, András
Sági, Judit C.
Egyed, Bálint
Péter, György
Butz, Henriett
Nyírő, Gábor
Müller, Judit
Kovács, Gábor T.
Szalai, Csaba
Semsei, Ágnes F.
Erdélyi, Dániel J.
author_facet Rzepiel, Andrea
Kutszegi, Nóra
Gézsi, András
Sági, Judit C.
Egyed, Bálint
Péter, György
Butz, Henriett
Nyírő, Gábor
Müller, Judit
Kovács, Gábor T.
Szalai, Csaba
Semsei, Ágnes F.
Erdélyi, Dániel J.
author_sort Rzepiel, Andrea
collection PubMed
description BACKGROUND: Treatment stratification based on bone marrow minimal residual disease (MRD) at set time points has resulted in considerably improved survival in pediatric acute lymphoblastic leukemia (ALL). Treatment response is assessed using bone marrow samples. MicroRNAs (miRs) easily traffic among fluid spaces and are more stable than most other RNA classes. We examined the role of circulating miRs as putative less invasive MRD biomarkers. METHODS: In an exploratory experiment, expression of 46 preselected miRs was studied in platelet-free blood plasma samples of 15 de novo, 5 relapsed ALL patients and 10 controls by Custom TaqMan Array Advanced MicroRNA Card. Based on their high expression in ALL compared to controls, and on the reduction observed along the induction therapy, four miRs were selected for further analyses: miR-128-3p, -181a-5p, -181b-5p and 222-3p. Their expression was measured by qPCR at 4 time points in 27 de novo ALL patients treated in the ALL IC-BFM 2009 study. RESULTS: The expression of all 4 miRs significantly decreased over the first week of therapy (miR-128-3p: log(2) fold change − 2.86; adjusted p 3.6 × 10(−7); miR-181b-5p: log(2) fold change − 1.75; adjusted p 1.48 × 10(−2); miR-181a-5p: log(2) fold change -1.33; adjusted p 3.12 × 10(−2); miR-222-3p: log(2) fold change − 1.25; adjusted p 1.66 × 10(−2)). However, no significant further reduction in miR expression was found after the 8th day of therapy. Measured drop in expression of 2 miRs at day 8 strongly correlated with day 15 bone marrow flow cytometry MRD results (miR-128-3p: Pearson’s r = 0.88, adjusted p = 2.71 × 10(−4); miR-222-3p: r = 0.81, adjusted p = 2.99 × 10(−3)). CONCLUSION: In conclusion, these circulating miRs might act as biomarkers of residual leukemia. MiR-128-3p and miR-222-3p in blood predict day 15 flow cytometry MRD results 7 days earlier. Although, their sensitivity falls behind that of bone marrow flow cytometry MRD at day 15.
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spelling pubmed-68546982019-11-21 Circulating microRNAs as minimal residual disease biomarkers in childhood acute lymphoblastic leukemia Rzepiel, Andrea Kutszegi, Nóra Gézsi, András Sági, Judit C. Egyed, Bálint Péter, György Butz, Henriett Nyírő, Gábor Müller, Judit Kovács, Gábor T. Szalai, Csaba Semsei, Ágnes F. Erdélyi, Dániel J. J Transl Med Research BACKGROUND: Treatment stratification based on bone marrow minimal residual disease (MRD) at set time points has resulted in considerably improved survival in pediatric acute lymphoblastic leukemia (ALL). Treatment response is assessed using bone marrow samples. MicroRNAs (miRs) easily traffic among fluid spaces and are more stable than most other RNA classes. We examined the role of circulating miRs as putative less invasive MRD biomarkers. METHODS: In an exploratory experiment, expression of 46 preselected miRs was studied in platelet-free blood plasma samples of 15 de novo, 5 relapsed ALL patients and 10 controls by Custom TaqMan Array Advanced MicroRNA Card. Based on their high expression in ALL compared to controls, and on the reduction observed along the induction therapy, four miRs were selected for further analyses: miR-128-3p, -181a-5p, -181b-5p and 222-3p. Their expression was measured by qPCR at 4 time points in 27 de novo ALL patients treated in the ALL IC-BFM 2009 study. RESULTS: The expression of all 4 miRs significantly decreased over the first week of therapy (miR-128-3p: log(2) fold change − 2.86; adjusted p 3.6 × 10(−7); miR-181b-5p: log(2) fold change − 1.75; adjusted p 1.48 × 10(−2); miR-181a-5p: log(2) fold change -1.33; adjusted p 3.12 × 10(−2); miR-222-3p: log(2) fold change − 1.25; adjusted p 1.66 × 10(−2)). However, no significant further reduction in miR expression was found after the 8th day of therapy. Measured drop in expression of 2 miRs at day 8 strongly correlated with day 15 bone marrow flow cytometry MRD results (miR-128-3p: Pearson’s r = 0.88, adjusted p = 2.71 × 10(−4); miR-222-3p: r = 0.81, adjusted p = 2.99 × 10(−3)). CONCLUSION: In conclusion, these circulating miRs might act as biomarkers of residual leukemia. MiR-128-3p and miR-222-3p in blood predict day 15 flow cytometry MRD results 7 days earlier. Although, their sensitivity falls behind that of bone marrow flow cytometry MRD at day 15. BioMed Central 2019-11-14 /pmc/articles/PMC6854698/ /pubmed/31727091 http://dx.doi.org/10.1186/s12967-019-2114-x Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Rzepiel, Andrea
Kutszegi, Nóra
Gézsi, András
Sági, Judit C.
Egyed, Bálint
Péter, György
Butz, Henriett
Nyírő, Gábor
Müller, Judit
Kovács, Gábor T.
Szalai, Csaba
Semsei, Ágnes F.
Erdélyi, Dániel J.
Circulating microRNAs as minimal residual disease biomarkers in childhood acute lymphoblastic leukemia
title Circulating microRNAs as minimal residual disease biomarkers in childhood acute lymphoblastic leukemia
title_full Circulating microRNAs as minimal residual disease biomarkers in childhood acute lymphoblastic leukemia
title_fullStr Circulating microRNAs as minimal residual disease biomarkers in childhood acute lymphoblastic leukemia
title_full_unstemmed Circulating microRNAs as minimal residual disease biomarkers in childhood acute lymphoblastic leukemia
title_short Circulating microRNAs as minimal residual disease biomarkers in childhood acute lymphoblastic leukemia
title_sort circulating micrornas as minimal residual disease biomarkers in childhood acute lymphoblastic leukemia
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6854698/
https://www.ncbi.nlm.nih.gov/pubmed/31727091
http://dx.doi.org/10.1186/s12967-019-2114-x
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