Experimental & Molecular Medicine · 2024 · 17 citations · 35 references
Life SciencesMolecular BiologyOncologyGene ExpressionMolecular OncologySignal TransductionCancer Cell SignalingHepatocellular CarcinomaOncogenic Signaling PathwaysSignal Transduction In CancerStress Signaling PathwaysStress-responsive Gene RegulationAdrenergic SignalingCellular Stress Signaling PathwaysEpinephrine SignalingPsychological Stress ResponseStress-activated Signaling PathwaysTherapeutic Target Identification
Hepatocellular carcinoma (HCC) is associated with a poor prognosis. Our previous study demonstrated that Pleomorphic adenoma gene like-2 (PLAGL2) was a potential therapeutic target in HCC. However, the mechanisms that lead to the upregulation of PLAGL2 in HCC remain unclear. The present study revealed that stress-induced epinephrine increased the expression of PLAGL2, thereby promoting the progression of HCC. Furthermore, PLAGL2 knockdown inhibited epinephrine-induced HCC development. Mechanistically, epinephrine upregulated ubiquitin-specific protease 10 (USP10) to stabilize PLAGL2 via the adrenergic β-receptor-2-c-Myc (ADRB2-c-Myc) axis. Furthermore, PLAGL2 acted as a transcriptional regulator of USP10, forming a signaling loop. Taken together, these results reveal that stress-induced epinephrine activates the PLAGL2-USP10 signaling loop to enhance HCC progression. Furthermore, PLAGL2 plays a crucial role in psychological stress-mediated promotion of HCC progression.
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Hallmarks of Cancer: New Dimensions
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