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Updated: Apr 23, 2026

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Analysis of Retinoic Acid-induced Neural Differentiation of Mouse Embryonic Stem Cells in Two and Three-dimensional Embryoid Bodies
Published on: April 22, 2017
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Retinoic Acid and Long Noncoding RNAs Crosstalk: Implications for Neuronal Differentiation and Diseases
Anita Kumari1,2, Pramod C Rath3
1Molecular Biology Laboratory, School of Life Sciences, Jawaharlal Nehru University, New Delhi, 110067, India.
Molecular Neurobiology
|April 21, 2026
Summary
Retinoic acid (RA) regulates gene expression by modulating long noncoding RNAs (lncRNAs). This crosstalk influences cell fate and disease, offering potential for new RNA-based therapies.
Area of Science:
- Molecular Biology
- Genetics
- Developmental Biology
Background:
- Retinoic acid (RA), a vitamin A metabolite, is a key signaling molecule controlling cell functions via nuclear receptors.
- Long noncoding RNAs (lncRNAs) are regulatory RNAs impacting gene expression through diverse mechanisms.
- Both RA signaling and lncRNA networks are implicated in aging and associated diseases.
Purpose of the Study:
- To review the mechanisms of RA-mediated modulation of lncRNA expression.
- To highlight the role of RA-lncRNA interactions in development, disease, and aging.
- To explore the therapeutic potential of targeting this crosstalk.
Main Methods:
- Literature review focusing on transcriptional and post-transcriptional regulation.
- Analysis of studies investigating RA-lncRNA interactions in various biological contexts.
- Synthesis of information on RNA-based therapeutic strategies.
Main Results:
- RA influences lncRNA expression through transcriptional and post-transcriptional regulation.
- The interplay between RA and lncRNAs is crucial for cell differentiation, tissue development, and disease pathogenesis.
- RA-lncRNA crosstalk is involved in aging and age-related diseases.
Conclusions:
- The intricate relationship between RA and lncRNAs is fundamental to normal development and disease processes.
- Understanding RA-lncRNA crosstalk opens avenues for novel RNA-based therapeutic interventions.
- Targeting RA-lncRNA interactions may offer promising treatments for age-related diseases.
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