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MicroRNA Signatures in Blood or Bone Marrow Distinguish Subtypes of Pediatric Acute Lymphoblastic Leukemia

OncomiRs are microRNAs that are associated with early onset of specific cancers. To identify microRNAs involved in pediatric acute lymphoblastic leukemia (ALL) subtypes T-ALL and B-ALL, peripheral blood and bone marrow samples were independently subjected to microarray analysis using two different h...

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Autores principales: Nair, Rekha A, Verma, Vinod Kumar, Beevi, Syed Sultan, Rawoof, Abdul, Alexander, Liza Esther, Prasad, E. Ramanjaneya, Kumari, P. Kusuma, Kumar, Prashant, Dinesh Kumar, Lekha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Neoplasia Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7292917/
https://www.ncbi.nlm.nih.gov/pubmed/32531485
http://dx.doi.org/10.1016/j.tranon.2020.100800
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author Nair, Rekha A
Verma, Vinod Kumar
Beevi, Syed Sultan
Rawoof, Abdul
Alexander, Liza Esther
Prasad, E. Ramanjaneya
Kumari, P. Kusuma
Kumar, Prashant
Dinesh Kumar, Lekha
author_facet Nair, Rekha A
Verma, Vinod Kumar
Beevi, Syed Sultan
Rawoof, Abdul
Alexander, Liza Esther
Prasad, E. Ramanjaneya
Kumari, P. Kusuma
Kumar, Prashant
Dinesh Kumar, Lekha
author_sort Nair, Rekha A
collection PubMed
description OncomiRs are microRNAs that are associated with early onset of specific cancers. To identify microRNAs involved in pediatric acute lymphoblastic leukemia (ALL) subtypes T-ALL and B-ALL, peripheral blood and bone marrow samples were independently subjected to microarray analysis using two different high-fidelity array platforms. The unique and common gene signatures from both arrays were validated by TaqMan individual assays in 100 pediatric ALL samples. Survival studies were carried out in the test set and validation set with 50 randomly selected samples in each set. MicroRNA expression profile revealed characteristic signatures for distinguishing T and B lineages and identified 51 novel microRNAs in pediatric ALL. Interestingly, the present study also revealed endogenous similarities and differences between blood and bone marrow within each ALL subtype. When Cox regression analysis was carried out with these identified microRNAs, 11 of them exhibited expression levels significantly correlated with survival. Validation of some of the common and relevant microRNAs from both arrays showed that their targets are involved in key oncogenic signaling pathways. Thus, this study suggests that microRNAs have the potential to become important diagnostic tools for identification and monitoring clinical outcomes in ALL patients.
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spelling pubmed-72929172020-06-17 MicroRNA Signatures in Blood or Bone Marrow Distinguish Subtypes of Pediatric Acute Lymphoblastic Leukemia Nair, Rekha A Verma, Vinod Kumar Beevi, Syed Sultan Rawoof, Abdul Alexander, Liza Esther Prasad, E. Ramanjaneya Kumari, P. Kusuma Kumar, Prashant Dinesh Kumar, Lekha Transl Oncol Original article OncomiRs are microRNAs that are associated with early onset of specific cancers. To identify microRNAs involved in pediatric acute lymphoblastic leukemia (ALL) subtypes T-ALL and B-ALL, peripheral blood and bone marrow samples were independently subjected to microarray analysis using two different high-fidelity array platforms. The unique and common gene signatures from both arrays were validated by TaqMan individual assays in 100 pediatric ALL samples. Survival studies were carried out in the test set and validation set with 50 randomly selected samples in each set. MicroRNA expression profile revealed characteristic signatures for distinguishing T and B lineages and identified 51 novel microRNAs in pediatric ALL. Interestingly, the present study also revealed endogenous similarities and differences between blood and bone marrow within each ALL subtype. When Cox regression analysis was carried out with these identified microRNAs, 11 of them exhibited expression levels significantly correlated with survival. Validation of some of the common and relevant microRNAs from both arrays showed that their targets are involved in key oncogenic signaling pathways. Thus, this study suggests that microRNAs have the potential to become important diagnostic tools for identification and monitoring clinical outcomes in ALL patients. Neoplasia Press 2020-06-09 /pmc/articles/PMC7292917/ /pubmed/32531485 http://dx.doi.org/10.1016/j.tranon.2020.100800 Text en © 2020 The Authors http://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 Original article
Nair, Rekha A
Verma, Vinod Kumar
Beevi, Syed Sultan
Rawoof, Abdul
Alexander, Liza Esther
Prasad, E. Ramanjaneya
Kumari, P. Kusuma
Kumar, Prashant
Dinesh Kumar, Lekha
MicroRNA Signatures in Blood or Bone Marrow Distinguish Subtypes of Pediatric Acute Lymphoblastic Leukemia
title MicroRNA Signatures in Blood or Bone Marrow Distinguish Subtypes of Pediatric Acute Lymphoblastic Leukemia
title_full MicroRNA Signatures in Blood or Bone Marrow Distinguish Subtypes of Pediatric Acute Lymphoblastic Leukemia
title_fullStr MicroRNA Signatures in Blood or Bone Marrow Distinguish Subtypes of Pediatric Acute Lymphoblastic Leukemia
title_full_unstemmed MicroRNA Signatures in Blood or Bone Marrow Distinguish Subtypes of Pediatric Acute Lymphoblastic Leukemia
title_short MicroRNA Signatures in Blood or Bone Marrow Distinguish Subtypes of Pediatric Acute Lymphoblastic Leukemia
title_sort microrna signatures in blood or bone marrow distinguish subtypes of pediatric acute lymphoblastic leukemia
topic Original article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7292917/
https://www.ncbi.nlm.nih.gov/pubmed/32531485
http://dx.doi.org/10.1016/j.tranon.2020.100800
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