Diagnostic value and cognitive regulatory roles of long non-coding RNA UCA1 in Alzheimer's disease

Background: To explore the diagnostic role and potential mechanism of serum lncRNA UCA1 in Alzheimer 's disease (AD). Methods: UCA1 concentration was determined using quantitative RT-PCR. The receiver operating characteristic curve was plotted to assess the diagnostic value. Cell viability and apoptotic capacity were assessed by cell counting kit -8 (CCK-8) and flow cytometry. Water maze experiments were used to test cognitive function in mice. The target genes of UCA1 were identified with a dual luciferase reporter assay. Functional and pathway analysis of miR-342-3p target genes was determined using enrichment analysis. Results: The concentration of UCA1 was elevated in the AD group and represented a diagnostic possibility of AD. The silenced UCA1 reduced the roles of A beta on viability and apoptosis of SH center dot SY5Y cells by sponging miR-342-3p. The impaired cognitive impairment was partly recovered by the knockdown of the UCA1/miR-342-3p axis. Potential targets of miR-342-3p were enriched in function and pathways related to AD progression. Conclusion: The UCA1/miR-342-3p axis contributed to the occurrence of AD by regulating cognitive ability.