Related Experiment Video
Updated: Nov 24, 2025

Analysis of Combinatorial miRNA Treatments to Regulate Cell Cycle and Angiogenesis
Published on: March 30, 2019
Up-regulated miR-155 is associated with poor prognosis in childhood acute lymphoblastic leukemia and promotes cell
Cong Liang1, Yu Li1, Li-Na Wang1
1Department of Pediatrics, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, People's Republic of China.
Insights
High miR-155 expression predicts poor prognosis in childhood acute lymphoblastic leukemia (ALL). This microRNA promotes ALL cell proliferation by targeting ZNF238, suggesting miR-155 as a potential prognostic biomarker.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Acute lymphoblastic leukemia (ALL) is a common childhood cancer.
- Identifying prognostic biomarkers is crucial for improving patient outcomes.
Purpose of the Study:
- To identify a novel microRNA (miRNA) for predicting the prognosis of childhood ALL.
- To explore the underlying mechanism of the identified miRNA in ALL.
Main Methods:
- Analysis of miRNA expression profiles from public databases (GEO).
- RT-PCR to measure miR-155 expression in ALL patients.
- In vitro studies using ALL cell lines to assess the effects of miR-155.
- Dual-luciferase reporter assay to confirm miR-155 target.
- MTT and flow cytometry to evaluate cell proliferation and apoptosis.
Main Results:
- miR-155 was significantly upregulated, while ZNF238 was downregulated in diagnosed ALL.
- High miR-155 expression correlated with poor prognosis.
- Overexpression of miR-155 enhanced ALL cell proliferation and inhibited apoptosis.
- miR-155 directly targets and downregulates ZNF238.
- Silencing ZNF238 promoted proliferation in ALL cells.
Conclusions:
- miR-155 shows potential as a biomarker for predicting childhood ALL prognosis.
- miR-155 promotes ALL cell proliferation by targeting ZNF238.
- ZNF238 may function as a tumor suppressor in childhood ALL.
Objectives:
Acute lymphoblastic leukemia (ALL) is one of the most common malignancies in children. Our aim was to identify a novel miRNA that can predict prognosis of childhood ALL patients and explore its potential mechanism.
Methods:
The miRNA expression profiles of childhood ALL were analyzed using GEO database and HiSeq instruments. The expression of miR-155 was examined by RT-PCR in 42 ALL patients. To investigate the role of miR-155 in ALL, four ALL cell lines (CEM-C1, Jurkat, MOLT-3 and MOLT-4) were transfected with miR-155 mimics, miR-155 inhibitors or corresponding controls. Dual-luciferase reporter system was applied to confirm the miR-155 target ZNF238. Moreover, proliferation and apoptosis were evaluated by MTT and flow cytometry.
Results:
Dataset GSE56489 and GSE23024 demonstrated that miR-155 was up-regulated and ZNF238 was down-regulated at diagnosis status of ALL. High miR-155 expression was associated with poor outcome. Overexpressed miR-155 promoted ALL cell proliferation and inhibited apoptosis. Dual-luciferase reporter result showed that miR-155 directly regulated ZNF238. Silencing ZNF238 promoted cell proliferation in ALL cells.
Discussion:
Our research indicating that miR-155 might possess potential value as a biomarker for predicting the prognosis of individuals. However, the role of ZNF238 in childhood ALL remain unknown. In the present study, we found the possible role of ZNF238 as a new tumor suppressor in ALL, which might be necessary for the antiproliferative functions of normal cells to counteract ALL formation.
Conclusion:
Our results propose that miR-155 is in association with poor prognosis of childhood ALL. Furthermore, miR-155 could promote cell proliferation targeting ZNF238.
Related Concept Videos
Abnormal Proliferation
mTOR Signaling and Cancer Progression
The mTOR pathway or the...
Negative Regulator Molecules
Induced Pluripotent Stem Cells
Somatic...
MicroRNAs
MicroRNAs

