Journal
ACTA BIOCHIMICA ET BIOPHYSICA SINICA
Volume 53, Issue 4, Pages 446-453Publisher
SCIENCE PRESS
DOI: 10.1093/abbs/gmab011
Keywords
lncRNA; LBX2-AS1; glioma; proliferation; migration
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Funding
- Tianjin Municipal Science and Technology Commission [20JCQNJC00410]
- Tianjin Jinnan District Science and Technology Project [20190103]
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This study demonstrated that LBX2-AS1 is significantly increased and negatively correlated with prognosis in glioma. Silencing LBX2-AS1 inhibited the proliferation, migration, and invasion of glioma cells and increased apoptosis. LBX2-AS1 was found to regulate the Akt/GSK3 beta pathway, making it a potential new target for glioma therapy.
Long non-coding RNAs (lncRNAs) have been proposed to play pivotal roles in the tumorigenesis of various malignant tumors. Previous studies have found that lncRNA LBX2-AS1 is involved in the progression of various tumors. However, currently, the expression and exact mechanism of LBX2-AS1 in glioma remain unclear. In this study, using online-available datasets combined with clinical glioma tissues collected, we found that LBX2-AS1 was significantly increased and negatively correlated with prognosis in glioma. In vitro functional assays such as CCK-8, Annexin V, transwell assay, and western blot analysis showed that silencing of LBX2-AS1 suppressed the proliferation, migration, and invasion of glioma cells and increased apoptosis. RNA sequencing and western blot analysis confirmed that LBX2-AS1 regulates the Akt/GSK3 beta pathway. In conclusion, this study showed that lncRNA LBX2-AS1 depletion inhibits the proliferation, migration, and invasion of glioma cells and increases apoptosis through the Akt/GSK3 beta pathway. lncRNA LBX2-AS1 is expected to become a new target for glioma therapy.
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