The Kaohsiung Journal of Medical Sciences · 2019 · 25 citations · 23 references
MedicineMolecular BiologyOncologyCell SignalingGene ExpressionMolecular OncologyCancer Cell SignalingCell-cycle DysregulationLung CancerOncogenic Signaling PathwaysTumor Suppressor Gene InactivationTumor Suppressor GenesCell Growth RegulationCyclin RegulationPi3k-akt Signaling PathwayPi3k-akt-mtor SignalingProtein Expression LevelsPten InactivationTumor Suppressor P53Tumor Suppressor Pathways
Ubiquitin-specific protease 44 (USP44) has been reported as a tumor suppressor or promoter in some tumors, but its function in non-small cell lung cancer (NSCLC) is still unclear. In this study, USP44 was found significantly downregulated in both of NSCLC tissues and cell lines, and low expression of USP44 predicted a poor prognosis for NSCLC patients. Overexpression of USP44 markedly downregulated the expression levels of Cyclin D1 and CDK4, but upregulated p53 expression, as a result of which, suppressing the cell growth of NSCLC cells. Further studies indicated that overexpression of USP44 significantly inhibited the phosphorylation of AKT, and its down-stream signals, including mTOR and P70S6K. Moreover, overexpression of USP44 increased PTEN protein but not its mRNA levels, which suggested that USP44 inhibited AKT signaling by stabilizing PTEN in NSCLC cells. In conclusion, we demonstrated that USP44 showed prior evidence of a tumor suppressive function in NSCLC cells, and inhibited NSCLC cell growth by suppressing AKT signaling, suggesting that USP44 could be as a novel target for NSCLC therapy.
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Non-Small Cell Lung Cancer: Epidemiology, Risk Factors, Treatment, and Survivorship
Julian R. Molina, Ping Yang, Stephen D. Cassivi et al. · Mayo Clinic Proceedings · 2008 · 2.9K citations