Identification of the circ_PRKDC/miR‐20a‐3p/RASA1 axis in regulating HaCaT keratinocyte migration.

Migration of keratinocytes plays a crucial role in the re‐epithelialization phase during wound healing. Circular RNA (circRNA) protein kinase, DNA‐activated, catalytic subunit (circ_PRKDC, hsa_circ_0084443) has been identified as a regulator of keratinocyte migration. However, the molecular basis go...

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Publicado en:Wound Repair & Regeneration Vol. 30; no. 2; pp. 282 - 292
Autores principales: Jiang, Li‐na, Ji, Xiaohui, Liu, Wei, Qi, Chuanchuan, Zhai, Xiaomei
Formato: pictorial research tables/charts Journal Article
Publicado: Wiley-Blackwell Mar2022
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Mar2022
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      pub: Wiley-Blackwell
      place: Malden, Massachusetts
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        10.1111/wrr.12988
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        atl: Identification of the circ_PRKDC/miR‐20a‐3p/RASA1 axis in regulating HaCaT keratinocyte migration.
      aug:
        au:
          Jiang, Li‐na
          Ji, Xiaohui
          Liu, Wei
          Qi, Chuanchuan
          Zhai, Xiaomei
        affil: Department of Plastic Surgery, The First Affiliated Hospital of Zhengzhou University, Zhengzhou Henan,, China
      sug:
        subj:
          RNA, Circular Physiology
          MicroRNA Physiology
          Keratinocytes Physiology
          Protein Kinases Physiology
          DNA Physiology
          Cell Movement
          Molecular Biology
          Human
          Wound Healing
          Skin Physiology
          RNA, Circular Blood
          MicroRNA Blood
          Polymerase Chain Reaction Methods
          Blotting, Western
          Cell Migration Assays Methods
          Gene Expression
          Transcription Factors
      ab: Migration of keratinocytes plays a crucial role in the re‐epithelialization phase during wound healing. Circular RNA (circRNA) protein kinase, DNA‐activated, catalytic subunit (circ_PRKDC, hsa_circ_0084443) has been identified as a regulator of keratinocyte migration. However, the molecular basis governing it remains unclear. The levels of circ_PRKDC, microRNA (miR)‐20a‐3p, and RAS p21 protein activator 1 (RASA1) were assessed by quantitative real‐time PCR (qRT‐PCR) or western blot. Subcellular localization, Actinomycin D, and Ribonuclease (RNase) R assays were performed to characterise circ_PRKDC. Cell migration was gauged by transwell and wound‐healing assays. A direct relationship between miR‐20a‐3p and circ_PRKDC or RASA1 was verified by dual‐luciferase reporter and RNA pull‐down assays. Circ_PRKDC expression was reduced in wound skin during wound healing. Circ_PRKDC modulated migration of HaCaT keratinocytes. Mechanistically, circ_PRKDC directly targeted miR‐20a‐3p. The regulation of circ_PRKDC on HaCaT keratinocyte migration was mediated by miR‐20a‐3p. RASA1 was identified as a direct and functional target of miR‐20a‐3p, and miR‐20a‐3p‐mediated inhibition of RASA1 impacted HaCaT keratinocyte migration. Circ_PRKDC acted as a post‐transcriptional modulator of RASA1 expression through miR‐20a‐3p. Moreover, circ_PRKDC modulated migration of HaCaT keratinocytes by RASA1. Our findings demonstrated a novel molecular basis, the miR‐20a‐3p/RASA1 axis, for the regulation of circ_PRKDC on HaCaT keratinocyte migration.
      pubtype: Academic Journal
      doctype:
        pictorial
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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