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Updated: May 24, 2026

Analysis of Combinatorial miRNA Treatments to Regulate Cell Cycle and Angiogenesis
Published on: March 30, 2019
Oncomir miR-125b regulates hematopoiesis by targeting the gene Lin28A
Aadel A Chaudhuri1, Alex Yick-Lun So, Arnav Mehta
1Departments of Biology and Computing and Mathematical Sciences, California Institute of Technology, Pasadena, CA 91125, USA.
Abstract:
MicroRNA-125b (miR-125b) is up-regulated in patients with leukemia. Overexpression of miR-125b alone in mice causes a very aggressive, transplantable myeloid leukemia. Before leukemia, these mice do not display elevation of white blood cells in the spleen or bone marrow; rather, the hematopoietic compartment shows lineage-skewing, with myeloid cell numbers dramatically increased and B-cell numbers severely diminished. miR-125b exerts this effect by up-regulating the number of common myeloid progenitors while inhibiting development of pre-B cells. We applied a miR-125b sponge loss of function system in vivo to show that miR-125b physiologically regulates hematopoietic development. Investigating the mechanism by which miR-125b regulates hematopoiesis, we found that, among a panel of candidate targets, the mRNA for Lin28A, an induced pluripotent stem cell gene, was most repressed by miR-125b in mouse hematopoietic stem and progenitor cells. Overexpressing Lin28A in the mouse hematopoietic system mimicked the phenotype observed on inhibiting miR-125b function, leading to a decrease in hematopoietic output. Relevant to the miR-125b overexpression phenotype, we also found that knockdown of Lin28A led to hematopoietic lineage-skewing, with increased myeloid and decreased B-cell numbers. Thus, the miR-125b target Lin28A is an important regulator of hematopoiesis and a primary target of miR-125b in the hematopoietic system.
Insights
MicroRNA-125b (miR-125b) drives aggressive myeloid leukemia by skewing hematopoietic development. It increases myeloid progenitors and decreases B-cells, primarily by repressing the Lin28A gene.
Area of Science:
- Hematology
- Molecular Biology
- Oncology
Background:
- MicroRNA-125b (miR-125b) is elevated in leukemia patients.
- Overexpression of miR-125b in mice induces aggressive myeloid leukemia.
Purpose of the Study:
- To investigate the role of miR-125b in hematopoietic development and leukemia.
- To identify the molecular targets of miR-125b in hematopoiesis.
Main Methods:
- Utilized a miR-125b sponge loss-of-function system in vivo.
- Analyzed hematopoietic stem and progenitor cells for gene expression changes.
- Overexpressed and knocked down Lin28A to assess its role in hematopoiesis.
Main Results:
- miR-125b overexpression caused myeloid leukemia with skewed hematopoiesis (increased myeloid, decreased B-cells).
- miR-125b was found to repress Lin28A mRNA in hematopoietic stem and progenitor cells.
- Lin28A manipulation mimicked or reversed miR-125b-induced hematopoietic changes.
Conclusions:
- miR-125b is a key regulator of hematopoietic development.
- Lin28A is a critical target of miR-125b in the hematopoietic system.
- The miR-125b/Lin28A axis plays a significant role in myeloid leukemia pathogenesis.
Related Concept Videos
MicroRNAs
MicroRNAs
Regulation of Hematopoietic Stem Cells
lncRNA - Long Non-coding RNAs
Hematopoiesis
Lineage Commitment

