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Published on: February 17, 2021
LncRNA-miRNA-mRNA regulatory networks in skin aging and therapeutic potentials
1Center for RNA Research, Institute for Basic Science, Seoul, Republic of Korea.
Abstract:
Skin aging is a complex process influenced by intrinsic and extrinsic factors. Although dermatology offers advanced interventions, molecular mechanisms in skin aging remain limited. Competing endogenous RNAs (ceRNAs), a subset of coding or non-coding RNAs, regulate gene expression through miRNA competition. Several ceRNA networks investigated up to now offer insights into skin aging and wound healing. In skin aging, RP11-670E13.6-miR-663a-CDK4/CD6 delays senescence induced by UVB radiation. Meg3-miR-93-5p-epiregulin contributes to UVB-induced inflammatory skin damage. Predicted ceRNA networks reveal UVA-induced photoaging mechanisms. SPRR2C sequesters miRNAs in epidermal aging-associated alteration of calcium gradient. H19-miR-296-5p-IGF2 regulates dermal fibroblast senescence. PVT1-miR-551b-3p-AQP3 influences skin photoaging. And bioinformatics analyses identify critical genes and compounds for skin aging interventions. In skin wound healing, MALAT1-miR-124 aids wound healing by activating the Wnt/β-catenin pathway. Hair follicle MSC-derived H19 promotes wound healing by inhibiting pyroptosis. And the SAN-miR-143-3p-ADD3 network rejuvenates adipose-derived mesenchymal stem cells in wound healing. Thus, ceRNA networks provide valuable insights into the molecular underpinnings of skin aging and wound healing, offering potential therapeutic strategies for further investigation. This comprehensive review serves as a foundational platform for future research endeavors in these crucial areas of dermatology.
Insights
Competing endogenous RNA (ceRNA) networks offer new molecular insights into skin aging and wound healing. Understanding these ceRNA networks can guide future dermatological interventions and therapeutic strategies.
Area of Science:
- Molecular biology
- Dermatology
- Genetics
Background:
- Skin aging involves intrinsic and extrinsic factors, with limited understanding of its molecular mechanisms.
- Competing endogenous RNA (ceRNA) networks, regulating gene expression via miRNA competition, are emerging as key players.
- Existing research highlights ceRNA roles in skin aging and wound healing, but a comprehensive overview is needed.
Purpose of the Study:
- To review and synthesize current knowledge on ceRNA networks in skin aging and wound healing.
- To identify specific ceRNA interactions and their roles in these processes.
- To highlight the potential of ceRNA networks as therapeutic targets in dermatology.
Main Methods:
- Literature review of studies investigating ceRNA networks in skin aging and wound healing.
- Analysis of identified ceRNA interactions, including specific RNAs, miRNAs, and target genes.
- Bioinformatic approaches used to predict and validate ceRNA networks.
Main Results:
- Several ceRNA networks implicated in skin aging, such as RP11-670E13.6-miR-663a-CDK4/CD6, Meg3-miR-93-5p-epiregulin, H19-miR-296-5p-IGF2, and PVT1-miR-551b-3p-AQP3.
- ceRNA networks involved in wound healing, including MALAT1-miR-124, H19, and SAN-miR-143-3p-ADD3.
- Identification of critical genes and compounds for skin aging interventions through bioinformatics.
Conclusions:
- ceRNA networks are crucial for understanding the molecular basis of skin aging and wound healing.
- These networks offer promising therapeutic strategies for dermatological conditions.
- Further research into ceRNA mechanisms can advance regenerative medicine and anti-aging therapies.
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