Long non-coding RNAs (lncRNAs) serve an important role in
tumor progression, and their abnormal expression is associated with
tumor development. The
lncRNA narcolepsy candidate region 1 gene C (lnc-NLC1-C) is involved in numerous types of
cancer, but its biological function in
glioma remains unknown. In the present study, lnc-NLC1-C expression was detected using reverse transcription-quantitative (RT-q)PCR in U251, SHG44, U87MG and U118MG
glioma cells. U87MG cells were transfected with lnc-NLC1-C overexpression or interference vectors. Cell proliferation was detected using a Cell Counting Kit-8 assay. Cell migration and invasion were examined using a Transwell assay, while apoptosis, cell cycle and
reactive oxygen species production were evaluated using flow cytometry, and the expression levels of lnc-NLC1-C,
microRNA (miR)-383 and
peroxiredoxin 3 (PRDX-3) were measured using western blotting and RT-qPCR. Rescue experiments were performed to verify the function of the lnc-NLC1-C/miR-383/PRDX-3 axis. The highest expression levels of lnc-NLC1-C were identified in U87MG
glioma cells. Overexpression of lnc-NLC1-C expression promoted cell proliferation, G1 phase blocking, migration and invasion, while inhibiting apoptosis and autophagy in U87MG cells. Mechanistically, miR-383 could bind to lnc-NLC1-C to regulate PRDX-3 expression and improve its oncogenic effect. Rescue experiments confirmed that the lnc-NLC1-C/miR-383/PRDX-3 axis was involved in the molecular mechanism of
glioma progression. Therefore, lnc-NLC1-C may be a
tumor promoter that affects multiple biological functions, such as migration, invasion and autophagy, in
glioma cells.