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Updated: Aug 19, 2026

Proliferation and Differentiation of Murine Myeloid Precursor 32D/G-CSF-R Cells
Published on: February 21, 2018
Coexpression and regulation of the FGF-2 and FGF antisense genes in leukemic cells
Mark Baguma-Nibasheka1, Audrey W Li, Mohammed S Osman
1Department of Physiology and Biophysics, Faculty of Medicine, Dalhousie University, 5850 College Street, Halifax, Nova Scotia, Canada B3H 1X5.
Abstract:
Fibroblast growth factor-2 (FGF-2) is a growth and survival factor whose expression is elevated in many hematopoietic malignancies. A natural antisense RNA (FGF-AS) has been implicated in the posttranscriptional regulation of FGF-2 mRNA expression. We demonstrate for the first time that FGF sense and antisense RNAs are coordinately expressed and translated in hematopoietic cells and tissues. Cytokine stimulation of growth-arrested K562 cells elicited a rapid transient increase in FGF-AS mRNA expression followed by a slower but sustained increase in FGF-2 mRNA. This was accompanied by a marked increase in the expression and nuclear translocation of FGF-2 and the FGF-AS encoded protein, GFG/NUDT6. These findings suggest a role for both FGF-2 and GFG proteins in the cell survival and proliferation of lymphoid and myeloid tumor cells.
Insights
Fibroblast growth factor-2 (FGF-2) and its antisense RNA (FGF-AS) are coordinately expressed in hematopoietic cells. This suggests both proteins play a role in lymphoid and myeloid tumor cell survival and proliferation.
Area of Science:
- Molecular Biology
- Hematology
- Cancer Biology
Background:
- Fibroblast growth factor-2 (FGF-2) is a key regulator of cell growth and survival.
- Elevated FGF-2 expression is observed in various hematopoietic malignancies.
- Natural antisense RNAs, like FGF-AS, are involved in posttranscriptional gene regulation.
Purpose of the Study:
- To investigate the coordinated expression and translation of FGF-2 and FGF-AS in hematopoietic cells.
- To elucidate the functional roles of FGF-2 and its antisense RNA in lymphoid and myeloid tumor cells.
Main Methods:
- Analysis of FGF sense and antisense RNA expression in hematopoietic cells and tissues.
- Cytokine stimulation of K562 cells to study mRNA and protein expression dynamics.
- Assessment of FGF-2 and GFG/NUDT6 protein expression and subcellular localization.
Main Results:
- Demonstrated coordinate expression and translation of FGF-2 and FGF-AS RNAs in hematopoietic cells.
- Observed rapid, transient increase in FGF-AS mRNA followed by sustained FGF-2 mRNA increase upon cytokine stimulation.
- Documented increased expression and nuclear translocation of FGF-2 and the FGF-AS encoded protein, GFG/NUDT6.
Conclusions:
- FGF-2 and GFG/NUDT6 proteins are likely involved in the survival and proliferation of lymphoid and myeloid tumor cells.
- The coordinated expression of FGF-2 and FGF-AS suggests a regulatory mechanism influencing hematopoietic malignancy progression.
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