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Volumn 47, Issue 5, 2015, Pages 1912-1922

Cantharidin and norcantharidin impair stemness of pancreatic cancer cells by repressing the β-catenin pathway and strengthen the cytotoxicity of gemcitabine and erlotinib

Author keywords

Cancer stem cells; Cantharidin; Pancreatic cancer; PP2A; catenin

Indexed keywords

ACTIVATED LEUKOCYTE CELL ADHESION MOLECULE; BETA CATENIN; BMI1 PROTEIN; CANTHARIDIN; CD24 ANTIGEN; CHEMOKINE RECEPTOR CXCR4; CYSTEINE RICH PROTEIN 61; EPHRIN RECEPTOR A2; EPIDERMAL GROWTH FACTOR RECEPTOR 3; EPITHELIAL CELL ADHESION MOLECULE; ERLOTINIB; GEMCITABINE; HERMES ANTIGEN; HIGH MOBILITY GROUP A2 PROTEIN; HYPOXIA INDUCIBLE FACTOR 1ALPHA; KRUPPEL LIKE FACTOR 4; KRUPPEL LIKE FACTOR 5; MESSENGER RNA; MULTIDRUG RESISTANCE PROTEIN 1; NORCANTHARIDIN; SMAD3 PROTEIN; TRANSCRIPTION FACTOR EZH2; TRANSCRIPTION FACTOR HES 1; TRANSCRIPTION FACTOR MSX2; TRANSCRIPTION FACTOR NANOG; TRANSCRIPTION FACTOR SOX2; TRANSCRIPTION FACTOR SOX9; DEOXYCYTIDINE; FUSED HETEROCYCLIC RINGS;

EID: 84942846318     PISSN: 10196439     EISSN: 17912423     Source Type: Journal    
DOI: 10.3892/ijo.2015.3156     Document Type: Article
Times cited : (36)

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