Evaluation of acute myeloid leukemia blast percentage on MethylC-Capture Sequencing results

Abstract Aberrant DNA methylation is often related to the diagnosis, prognosis, and therapeutic response of acute myeloid leukemia (AML); however, relevant studies on the relationship between bone marrow myeloblast percentage and the DNA methylation level in AML have not been reported. We evaluated...

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Main Authors: Erna Yang, Desheng Gong, Wei Guan, Jieying Li, Xuefeng Gao, Yonghui Li, Li Yu
Format: Article
Language:English
Published: BMC 2021-03-01
Series:Experimental Hematology & Oncology
Subjects:
Online Access:https://doi.org/10.1186/s40164-021-00219-0
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author Erna Yang
Desheng Gong
Wei Guan
Jieying Li
Xuefeng Gao
Yonghui Li
Li Yu
author_facet Erna Yang
Desheng Gong
Wei Guan
Jieying Li
Xuefeng Gao
Yonghui Li
Li Yu
author_sort Erna Yang
collection DOAJ
description Abstract Aberrant DNA methylation is often related to the diagnosis, prognosis, and therapeutic response of acute myeloid leukemia (AML); however, relevant studies on the relationship between bone marrow myeloblast percentage and the DNA methylation level in AML have not been reported. We evaluated the effects of AML blast percentage on DNA methylation level using the MethylC-capture sequencing (MCC-Seq) approach based on next-generation sequencing (NGS) and found that the methylation level of both genome-wide and promoter regions significantly increased when the percentage of AML blasts reached ≥ 40%, indicating that an accurate DNA methylation level in cancer cells can be obtained when the bone marrow samples of AML patients have more than 40% myeloblasts.
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spelling doaj.art-6edce62404374ce99dbc92c8e8c007f72022-12-21T18:53:13ZengBMCExperimental Hematology & Oncology2162-36192021-03-011011410.1186/s40164-021-00219-0Evaluation of acute myeloid leukemia blast percentage on MethylC-Capture Sequencing resultsErna Yang0Desheng Gong1Wei Guan2Jieying Li3Xuefeng Gao4Yonghui Li5Li Yu6Department of Hematology and Oncology, International Cancer Center, Shenzhen Key Laboratory of Precision Medicine for Hematological Malignancies, Shenzhen University General Hospital, Shenzhen University Clinical Medical Academy, Shenzhen University Health Science Center, Shenzhen UniversityDepartment of Hematology and Oncology, International Cancer Center, Shenzhen Key Laboratory of Precision Medicine for Hematological Malignancies, Shenzhen University General Hospital, Shenzhen University Clinical Medical Academy, Shenzhen University Health Science Center, Shenzhen UniversityDepartment of Hematology, Chinese PLA General HospitalDepartment of Hematology and Oncology, International Cancer Center, Shenzhen Key Laboratory of Precision Medicine for Hematological Malignancies, Shenzhen University General Hospital, Shenzhen University Clinical Medical Academy, Shenzhen University Health Science Center, Shenzhen UniversityCentrol Laboratory, Shenzhen University General Hospital, Shenzhen University Health Science CenterCentrol Laboratory, Shenzhen University General Hospital, Shenzhen University Health Science CenterDepartment of Hematology and Oncology, International Cancer Center, Shenzhen Key Laboratory of Precision Medicine for Hematological Malignancies, Shenzhen University General Hospital, Shenzhen University Clinical Medical Academy, Shenzhen University Health Science Center, Shenzhen UniversityAbstract Aberrant DNA methylation is often related to the diagnosis, prognosis, and therapeutic response of acute myeloid leukemia (AML); however, relevant studies on the relationship between bone marrow myeloblast percentage and the DNA methylation level in AML have not been reported. We evaluated the effects of AML blast percentage on DNA methylation level using the MethylC-capture sequencing (MCC-Seq) approach based on next-generation sequencing (NGS) and found that the methylation level of both genome-wide and promoter regions significantly increased when the percentage of AML blasts reached ≥ 40%, indicating that an accurate DNA methylation level in cancer cells can be obtained when the bone marrow samples of AML patients have more than 40% myeloblasts.https://doi.org/10.1186/s40164-021-00219-0AMLBlast percentageMethylation statusMCC-Seq
spellingShingle Erna Yang
Desheng Gong
Wei Guan
Jieying Li
Xuefeng Gao
Yonghui Li
Li Yu
Evaluation of acute myeloid leukemia blast percentage on MethylC-Capture Sequencing results
Experimental Hematology & Oncology
AML
Blast percentage
Methylation status
MCC-Seq
title Evaluation of acute myeloid leukemia blast percentage on MethylC-Capture Sequencing results
title_full Evaluation of acute myeloid leukemia blast percentage on MethylC-Capture Sequencing results
title_fullStr Evaluation of acute myeloid leukemia blast percentage on MethylC-Capture Sequencing results
title_full_unstemmed Evaluation of acute myeloid leukemia blast percentage on MethylC-Capture Sequencing results
title_short Evaluation of acute myeloid leukemia blast percentage on MethylC-Capture Sequencing results
title_sort evaluation of acute myeloid leukemia blast percentage on methylc capture sequencing results
topic AML
Blast percentage
Methylation status
MCC-Seq
url https://doi.org/10.1186/s40164-021-00219-0
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AT jieyingli evaluationofacutemyeloidleukemiablastpercentageonmethylccapturesequencingresults
AT xuefenggao evaluationofacutemyeloidleukemiablastpercentageonmethylccapturesequencingresults
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