Tehran University of Medical Sciences

Science Communicator Platform

Stay connected! Follow us on X network (Twitter):
Share this content! On (X network) By
Snhg14 Lncrna As a Prognostic Biomarker in Adult Non-M3 Aml Patients Publisher Pubmed



Seifpour S1 ; Zomorrod MS1 ; Atashi A2 ; Khaseb S1 ; Tavangar F3 ; Vajari MK4 ; Ahmadvand M5
Authors
Show Affiliations
Authors Affiliations
  1. 1. Department of Hematology, Faculty of Medical Sciences, Tarbiat Modares University (TMU), Tehran, Iran
  2. 2. Stem Cell and Tissue Engineering Research Center, Shahroud University of Medical Sciences, Iran
  3. 3. Iranian Blood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine, Tehran, Iran
  4. 4. Department of Hematology and Blood Banking, School of Allied Medical Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  5. 5. Cell Therapy and Hematopoietic Stem Cell Transplantation Research Center, Tehran University of Medical Sciences, Tehran, Iran

Source: Hematology/oncology and stem cell therapy Published:2025


Abstract

BACKGROUND AND OBJECTIVES: Acute myeloid leukemia (AML) is one of the most common blood malignancies in adults, characterized by the involvement of hematopoietic myeloid progenitors. Numerous studies have demonstrated the involvement of long noncoding RNAs (lncRNAs) in AML pathogenesis. This study aimed to investigate the expression profile of lncRNA small nuclear RNA host gene 14 (SNHG14) and its role in the pathogenesis, clinical features, and prognosis of adult non-M3 AML. MATERIALS AND METHODS: The expression level of SNHG14 was evaluated in bone marrow (BM) samples obtained from 50 adult non-M3 AML patients and 49 healthy controls using Quantitative Reverse Transcription-Polymerase Chain Reaction. We also investigated the correlation between clinicopathological characteristics and SNHG14 expression levels in AML patients. RESULTS: The expression level of SNHG14 was significantly decreased in the BM tissues of adult non-M3 AML patients compared to healthy controls. Patients with low SNHG14 expression were associated with poor overall survival, while no correlation was found between low SNHG14 expression and relapse-free survival. CONCLUSION: Our findings suggest that SNHG14 expression could serve as a potential biomarker for prognosing adult non-M3 AML patients. Furthermore, SNHG14 may offer insights into novel therapeutic targets for this subset of AML patients. Copyright © 2025 Hematology/Oncology and Stem Cell Therapy.