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Prognostic significance of long non coding maternally expressed gene 3 in pediatric acute myeloid leukemia.
Xue, Hongjuan; Gao, Haili; Xia, Hong; Li, Shaofei; Li, Na; Duan, Yuwen; Ren, Yanfei; Zhang, Henglu; Liu, Jingzheng; Gao, Wei.
Affiliation
  • Xue H; Department of Pediatric Hematology and Oncology, Xingtai People's Hospital, Xingtai, China.
  • Gao H; Department of Pediatric Hematology and Oncology, The Children's Hospital Affiliated of Zhengzhou University, Zhengzhou, China.
  • Xia H; Department of Pediatric, Xingtai People's Hospital, Xingtai, China.
  • Li S; Department of Digestive Endoscopy, Minmetals Hanxing General Hospital, Handan, China.
  • Li N; Department of Pediatric Hematology and Oncology, Xingtai People's Hospital, Xingtai, China.
  • Duan Y; Department of Pediatric Hematology and Oncology, Xingtai People's Hospital, Xingtai, China.
  • Ren Y; Department of Pediatric Hematology and Oncology, Xingtai People's Hospital, Xingtai, China.
  • Zhang H; Department of Pediatric Hematology and Oncology, Xingtai People's Hospital, Xingtai, China.
  • Liu J; Department of Pediatric Hematology and Oncology, The Central Hospital of Enshi Tujia and Miao Autonomous Prefecture, Enshi, China.
  • Gao W; Department of Pediatric Hematology and Oncology, Xingtai People's Hospital, Xingtai, China.
Medicine (Baltimore) ; 100(35): e26959, 2021 Sep 03.
Article in En | MEDLINE | ID: mdl-34477125
ABSTRACT: The purpose of this study was to evaluate the correlation of long non-coding RNA maternally expressed gene 3 (Lnc-MEG3) with disease features, treatment response, and survival in pediatric acute myeloid leukemia (AML) patients.Among 92 de novo pediatric AML patients (before treatment and after 1 course of induction) and 40 controls, bone marrow mononuclear cells were obtained. Then, Lnc-MEG3 expression was determined by reverse transcription quantitative polymerase chain reaction. After 1 course of standard induction therapy of pediatric AML patients, complete remission (CR) was assessed. Furthermore, event-free survival (EFS) and overall survival (OS) were determined according to follow-up data.Lnc-MEG3 was reduced in pediatric AML patients compared with controls. In pediatric AML patients, Lnc-MEG3 was correlated with French-American-Britain subtypes and lower Chinese Medical Association risk stratification, while it was not associated with cytogenetic features, FLT3-ITD mutation, CEBPA mutation, NPM1 mutation, WT1 mutation, or National Comprehensive Cancer Network risk stratification. After 1 course of treatment, Lnc-MEG3 exhibited an up-regulation trend. Furthermore, Lnc-MEG3 was of no difference before treatment between patients with and without CR, while elevated Lnc-MEG3 and change of Lnc-MEG3 after 1 course of treatment were associated with increased CR rate. Additionally, increased Lnc-MEG3 expression before treatment was associated with longer EFS but not OS, while enhanced Lnc-MEG3 expression after 1 course of treatment was correlated with both prolonged EFS and OS.Lnc-MEG3 may have clinical significance as a biomarker for assisting with disease management, treatment optimization, and prognosis improvement in pediatric AML patients.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Biomarkers, Tumor / Leukemia, Myeloid / RNA, Long Noncoding Type of study: Prognostic_studies Language: En Journal: Medicine (Baltimore) Year: 2021 Type: Article Affiliation country: China

Full text: 1 Database: MEDLINE Main subject: Biomarkers, Tumor / Leukemia, Myeloid / RNA, Long Noncoding Type of study: Prognostic_studies Language: En Journal: Medicine (Baltimore) Year: 2021 Type: Article Affiliation country: China