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Specific lncRNA signatures discriminate childhood acute leukaemias: a pilot study
BACKGROUND: Long non-coding RNAs are RNAs longer than 200 bps that do not encode any proteins and are able to alter gene expression by acting on different steps of regulation, including DNA methylation and chromatin structure. They represent a class of biomarkers of crescent interest in the hematolo...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9710039/ https://www.ncbi.nlm.nih.gov/pubmed/36451206 http://dx.doi.org/10.1186/s12935-022-02789-3 |
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author | Buono, Lorena Iside, Concetta De Matteo, Antonia Stellato, Pio Beneduce, Giuliana de Vera d’Aragona, Roberta Penta Parasole, Rosanna Salvatore, Marco Smaldone, Giovanni Mirabelli, Peppino |
author_facet | Buono, Lorena Iside, Concetta De Matteo, Antonia Stellato, Pio Beneduce, Giuliana de Vera d’Aragona, Roberta Penta Parasole, Rosanna Salvatore, Marco Smaldone, Giovanni Mirabelli, Peppino |
author_sort | Buono, Lorena |
collection | PubMed |
description | BACKGROUND: Long non-coding RNAs are RNAs longer than 200 bps that do not encode any proteins and are able to alter gene expression by acting on different steps of regulation, including DNA methylation and chromatin structure. They represent a class of biomarkers of crescent interest in the hematologic and oncologic fields. Recent studies showed that the expression levels of specific lncRNAs correlate with the prognosis of paediatric patients with Acute Lymphoblastic Leukaemia. METHODS: We used NGS approaches to analyse the transcriptome of 9 childhood B-ALL patients and 6 childhood T-ALL patients, in comparison with B and T healthy lymphocytes from cord blood. We validate our findings both ex vivo, in a different cohort of 10 B-ALL and 10 T-ALL patients, and in silico using public datasets. RESULTS: We characterised the lncRNA landscape for B-ALL, T-ALL, healthy B, and T cell progenitors. From the characterised signature, we selected candidate lncRNAs able to discriminate not only B-ALL and T-ALL from healthy subjects but also between the two types of leukaemia, and subsequently validated their potential as a diagnostic tool in an additional cohort of paediatric patients. We confirmed our finding with open access transcriptomic data, comparing ALL lncRNAs with AML lncRNA landscape as well. Finally, expression correlation analyses of T-ALL selected lncRNA biomarkers suggested a possible role in lymphocyte activation and the β-catenin signalling pathway for AC247036.1 and involvement in hedgehog signalling for HHIP-AS1. CONCLUSIONS: Our work identified a lncRNA signature discriminating paediatric B-ALL and T-ALL from healthy subjects, between them and from AML. This study provides the keystone to future clinical studies determining the theragnostic value of the characterised long non coding transcriptome panorama in a clinical setting for childhood patient management. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12935-022-02789-3. |
format | Online Article Text |
id | pubmed-9710039 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-97100392022-12-01 Specific lncRNA signatures discriminate childhood acute leukaemias: a pilot study Buono, Lorena Iside, Concetta De Matteo, Antonia Stellato, Pio Beneduce, Giuliana de Vera d’Aragona, Roberta Penta Parasole, Rosanna Salvatore, Marco Smaldone, Giovanni Mirabelli, Peppino Cancer Cell Int Research BACKGROUND: Long non-coding RNAs are RNAs longer than 200 bps that do not encode any proteins and are able to alter gene expression by acting on different steps of regulation, including DNA methylation and chromatin structure. They represent a class of biomarkers of crescent interest in the hematologic and oncologic fields. Recent studies showed that the expression levels of specific lncRNAs correlate with the prognosis of paediatric patients with Acute Lymphoblastic Leukaemia. METHODS: We used NGS approaches to analyse the transcriptome of 9 childhood B-ALL patients and 6 childhood T-ALL patients, in comparison with B and T healthy lymphocytes from cord blood. We validate our findings both ex vivo, in a different cohort of 10 B-ALL and 10 T-ALL patients, and in silico using public datasets. RESULTS: We characterised the lncRNA landscape for B-ALL, T-ALL, healthy B, and T cell progenitors. From the characterised signature, we selected candidate lncRNAs able to discriminate not only B-ALL and T-ALL from healthy subjects but also between the two types of leukaemia, and subsequently validated their potential as a diagnostic tool in an additional cohort of paediatric patients. We confirmed our finding with open access transcriptomic data, comparing ALL lncRNAs with AML lncRNA landscape as well. Finally, expression correlation analyses of T-ALL selected lncRNA biomarkers suggested a possible role in lymphocyte activation and the β-catenin signalling pathway for AC247036.1 and involvement in hedgehog signalling for HHIP-AS1. CONCLUSIONS: Our work identified a lncRNA signature discriminating paediatric B-ALL and T-ALL from healthy subjects, between them and from AML. This study provides the keystone to future clinical studies determining the theragnostic value of the characterised long non coding transcriptome panorama in a clinical setting for childhood patient management. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12935-022-02789-3. BioMed Central 2022-11-30 /pmc/articles/PMC9710039/ /pubmed/36451206 http://dx.doi.org/10.1186/s12935-022-02789-3 Text en © The Author(s) 2022 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 | Research Buono, Lorena Iside, Concetta De Matteo, Antonia Stellato, Pio Beneduce, Giuliana de Vera d’Aragona, Roberta Penta Parasole, Rosanna Salvatore, Marco Smaldone, Giovanni Mirabelli, Peppino Specific lncRNA signatures discriminate childhood acute leukaemias: a pilot study |
title | Specific lncRNA signatures discriminate childhood acute leukaemias: a pilot study |
title_full | Specific lncRNA signatures discriminate childhood acute leukaemias: a pilot study |
title_fullStr | Specific lncRNA signatures discriminate childhood acute leukaemias: a pilot study |
title_full_unstemmed | Specific lncRNA signatures discriminate childhood acute leukaemias: a pilot study |
title_short | Specific lncRNA signatures discriminate childhood acute leukaemias: a pilot study |
title_sort | specific lncrna signatures discriminate childhood acute leukaemias: a pilot study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9710039/ https://www.ncbi.nlm.nih.gov/pubmed/36451206 http://dx.doi.org/10.1186/s12935-022-02789-3 |
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