LncRNA FTX/OCT4/miR-122-5p orchestrates self-renewal and lineage commitment of human dental pulp stem cells by directly targeting FOXO3
LncRNA FTX overexpression exerts a suppressive effect on the transcriptional expression of miR-122-5p, which subsequently activates FOXO3 and thereby impedes cell proliferation as well as multilineage differentiation capacity of hDPSCs. Moreover, a novel lncRNA FTX-OCT4-miR-122-5p interaction pathway was discovered. These findings shed light on two novel regulatory mechanisms - lncRNA FTX/OCT4/miR-122-5p regulation and lncRNA FTX/miR-122-5p/FOXO3 regulation - that unravel crucial signaling pathways governing the pluripotency of hDPSCs, potentially offering promising RNA-based therapeutic strategies and gene-editing targets for dentin regeneration.
Authors
- Xi Wei (ORCID: https://orcid.org/0000-0002-5749-2910)
- Weini Xin (ORCID: https://orcid.org/0000-0001-5185-3722)
- Sui Mai (ORCID: https://orcid.org/0000-0002-2278-637X)
- Chen Cui (ORCID: https://orcid.org/0000-0002-9972-7343)
- Kai Zeng (ORCID: https://orcid.org/0000-0002-1738-6793)
- Lijing Wu
- Hong Hong (ORCID: https://orcid.org/0000-0002-1009-3621)
Institutions
- Sun Yat-sen University (CN)
- Shantou University (CN)
- Shantou University Medical College (CN)
- Stomatology Hospital (CN)
Publication Details
- Journal
- Stem Cell Research & Therapy
- Published
- 2025-10-15
- DOI
- https://doi.org/10.1186/s13287-025-04685-9
- Primary Topic
- Cancer-related molecular mechanisms research
- Type
- article
- Field-Weighted Citation Impact
- 0.00