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LncRNA-XIST Competitively Binds to MicroRNA-532-5p to Regulate PTEN Expression, Exacerbating Cerebral
Xudong Lu1,2, Luhan Chen1,2, Liqi Qian1,2
1Department of Neurology, Jiaxing Second Hospital, Jiaxing, Zhejiang, China.
Advanced Biology
|August 5, 2026
Summary
Long non-coding RNA-XIST promotes cerebral ischemia-reperfusion injury (CIRI) by targeting microRNA-532-5p and PTEN. Inhibiting lncRNA-XIST may offer a therapeutic strategy for CIRI.
Area of Science:
- Neuroscience
- Molecular Biology
- Genetics
Background:
- Cerebral ischemia-reperfusion injury (CIRI) is a significant neurological condition with unclear molecular mechanisms.
- Long non-coding RNA-XIST (lncRNA-XIST) has been implicated in CIRI, but its specific role and pathways are not fully understood.
Purpose of the Study:
- To elucidate the mechanism by which lncRNA-XIST contributes to cerebral ischemia-reperfusion injury.
- To investigate the regulatory axis involving lncRNA-XIST, microRNA-532-5p, and PTEN in CIRI.
Main Methods:
- Established middle cerebral artery occlusion/reperfusion (MCAO/R) rat and oxygen-glucose deprivation/reoxygenation (OGD/R) SH-SY5Y cell models.
- Utilized qPCR, bioinformatic prediction, dual-luciferase assays, CCK-8, flow cytometry, Western blot, and MDA/SOD assays to assess molecular changes and cellular responses.
- Investigated the expression levels of lncRNA-XIST, microRNA-532-5p, and PTEN.
Main Results:
- LncRNA-XIST and PTEN expression were elevated, while microRNA-532-5p was reduced in CIRI models.
- Knockdown of lncRNA-XIST mitigated OGD/R-induced cellular injury, apoptosis, and oxidative stress.
- LncRNA-XIST directly targets and inhibits microRNA-532-5p, which in turn targets and suppresses PTEN. This regulatory axis was confirmed through knockdown and rescue experiments.
Conclusions:
- LncRNA-XIST exacerbates cerebral ischemia-reperfusion injury through the microRNA-532-5p/PTEN pathway.
- Targeting the lncRNA-XIST/microRNA-532-5p/PTEN axis presents a potential therapeutic avenue for treating CIRI.
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