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BIOMARKER:

miR-324-5p overexpression

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Other names: MIR324, MicroRNA 324, Hsa-Mir-324, Hsa-MiR-324-5p, Hsa-MiR-324-3p, MIRN324
Entrez ID:
Related biomarkers:
over4years
MicroRNA-324-5p-CUEDC2 Axis Mediates Gain-of-Function Mutant p53-Driven Cancer Stemness. (PubMed, Mol Cancer Res)
Thus, our study delineates an altered miR-324-5p-CUEDC2-NF-κB pathway as a novel regulator of GOF mutant p53-driven cancer stemness. Implications: Our findings implicate microRNA-324-5p as a novel epigenetic modifier of human cancer stemness.
Journal
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TP53 (Tumor protein P53) • MYC (V-myc avian myelocytomatosis viral oncogene homolog) • MIR324 (MicroRNA 324)
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TP53 mutation • MYC expression • miR-324-5p overexpression
almost5years
Ginsenoside 20(S)-Rg3 suppresses cell viability in esophageal squamous cell carcinoma via modulating miR-324-5p-targeted PSME3. (PubMed, Hum Exp Toxicol)
Further exploration verified that miR-324-5p targeted PSME3, and PSME3 deficiency countervailed the effect of miR-324-5p inhibition on ESCC cell viability under 20(S)-Rg3 treatment. Conclusively, 20(S)-Rg3 suppresses cell viability in ESCC via mediating miR-324-5p-targeted PSME3.
Journal
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MIR324 (MicroRNA 324)
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miR-324-5p overexpression