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Serum circRNA_100199 is a Prognostic Biomarker in Acute Myeloid Leukemia

BACKGROUND: An aberrant level of serum microRNA expression has been demonstrated to be a prognostic marker for acute myeloid leukemia (AML). The therapeutic relevance of serum circRNA 100199 remained unknown, however. This research aimed to investigate the probable prognostic significance of serum c...

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Autores principales: Yan, Lingqiao, Yan, Qingxian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10588716/
https://www.ncbi.nlm.nih.gov/pubmed/37868816
http://dx.doi.org/10.2147/IJGM.S426218
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author Yan, Lingqiao
Yan, Qingxian
author_facet Yan, Lingqiao
Yan, Qingxian
author_sort Yan, Lingqiao
collection PubMed
description BACKGROUND: An aberrant level of serum microRNA expression has been demonstrated to be a prognostic marker for acute myeloid leukemia (AML). The therapeutic relevance of serum circRNA 100199 remained unknown, however. This research aimed to investigate the probable prognostic significance of serum circRNA_100199 for AML. METHODS: This study included a total of 200 participants consisting of 114 AML-diagnosed patients and 86 healthy people. Blood samples were taken, and the level of circRNA_100199 in the serum was measured using quantitative reverse transcription polymerase chain reaction (qRT-PCR) to explore its potential clinical significance. RESULTS: Our study demonstrated that circRNA_100199 expression in the serum was substantially higher in AML subjects than in healthy persons. This increase in serum circRNA_100199 levels was particularly noticeable in M4/M5 subtype AML patients, and those with poor cytogenetic risk or higher white blood cell counts. Using receiver operating characteristic (ROC) analysis, AML cases were effectively differentiated from healthy persons based on the level of serum circRNA_100199. Furthermore, it was found that high serum circRNA_100199 expression was strongly linked with shorter survival times and more severe clinical features. Our study also confirmed that high serum circRNA_100199 expression was an independent predictor of relapse-free survival (RFS) and overall survival (OS) in AML patients. Interestingly, the serum expression level of circRNA_100199 was significantly reduced following treatment, and its levels were substantially lower in AML patients who achieved complete remission (CR) than those who did not. CONCLUSION: Overall, these findings suggest that serum circRNA_100199 has the potential to be a favorable prognostic biomarker for AML.
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spelling pubmed-105887162023-10-21 Serum circRNA_100199 is a Prognostic Biomarker in Acute Myeloid Leukemia Yan, Lingqiao Yan, Qingxian Int J Gen Med Original Research BACKGROUND: An aberrant level of serum microRNA expression has been demonstrated to be a prognostic marker for acute myeloid leukemia (AML). The therapeutic relevance of serum circRNA 100199 remained unknown, however. This research aimed to investigate the probable prognostic significance of serum circRNA_100199 for AML. METHODS: This study included a total of 200 participants consisting of 114 AML-diagnosed patients and 86 healthy people. Blood samples were taken, and the level of circRNA_100199 in the serum was measured using quantitative reverse transcription polymerase chain reaction (qRT-PCR) to explore its potential clinical significance. RESULTS: Our study demonstrated that circRNA_100199 expression in the serum was substantially higher in AML subjects than in healthy persons. This increase in serum circRNA_100199 levels was particularly noticeable in M4/M5 subtype AML patients, and those with poor cytogenetic risk or higher white blood cell counts. Using receiver operating characteristic (ROC) analysis, AML cases were effectively differentiated from healthy persons based on the level of serum circRNA_100199. Furthermore, it was found that high serum circRNA_100199 expression was strongly linked with shorter survival times and more severe clinical features. Our study also confirmed that high serum circRNA_100199 expression was an independent predictor of relapse-free survival (RFS) and overall survival (OS) in AML patients. Interestingly, the serum expression level of circRNA_100199 was significantly reduced following treatment, and its levels were substantially lower in AML patients who achieved complete remission (CR) than those who did not. CONCLUSION: Overall, these findings suggest that serum circRNA_100199 has the potential to be a favorable prognostic biomarker for AML. Dove 2023-10-16 /pmc/articles/PMC10588716/ /pubmed/37868816 http://dx.doi.org/10.2147/IJGM.S426218 Text en © 2023 Yan and Yan. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Yan, Lingqiao
Yan, Qingxian
Serum circRNA_100199 is a Prognostic Biomarker in Acute Myeloid Leukemia
title Serum circRNA_100199 is a Prognostic Biomarker in Acute Myeloid Leukemia
title_full Serum circRNA_100199 is a Prognostic Biomarker in Acute Myeloid Leukemia
title_fullStr Serum circRNA_100199 is a Prognostic Biomarker in Acute Myeloid Leukemia
title_full_unstemmed Serum circRNA_100199 is a Prognostic Biomarker in Acute Myeloid Leukemia
title_short Serum circRNA_100199 is a Prognostic Biomarker in Acute Myeloid Leukemia
title_sort serum circrna_100199 is a prognostic biomarker in acute myeloid leukemia
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10588716/
https://www.ncbi.nlm.nih.gov/pubmed/37868816
http://dx.doi.org/10.2147/IJGM.S426218
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