The molecular mechanisms of XBP-1 gene silencing on IRE1α-TRAF2-ASK1-JNK pathways in oral squamous cell carcinoma under endoplasmic reticulum stress

Biomedicine and Pharmacotherapy

Volumn 77, Issue , 2016, Pages 108-113

  Chen, Haiying ^a,b   Yang, Hongli ^a   Pan, Li ^a   Wang, Weihua ^a   Liu, Xianbin ^a   Ren, Xiaoyan ^a   Liu, Yihua ^a   Liu, Wei ^a   Zhang, Yingxin ^a   Jiang, Licheng ^a   Li, Keyi ^a   Zhang, Bin ^a   Wang, Le xin ^c  

^a LIAOCHENG PEOPLE'S HOSPITAL   (China)

^b LIAOCHENG UNIVERSITY   (China)

^c CHARLES STURT UNIVERSITY   (Australia)

Author keywords

Apoptosis; MG132; Oral squamous cell carcinoma; Silencing; X box binding protein 1

Indexed keywords

APOPTOSIS SIGNAL REGULATING KINASE 1; BENZYLOXYCARBONYLLEUCYLLEUCYLLEUCINAL; PLASMID VECTOR; PROTEIN IRE1; PROTEIN IRE1ALPHA; SHORT HAIRPIN RNA; STRESS ACTIVATED PROTEIN KINASE; TUMOR NECROSIS FACTOR RECEPTOR ASSOCIATED FACTOR 2; UNCLASSIFIED DRUG; X BOX BINDING PROTEIN 1; BENZYLOXYCARBONYLLEUCYL-LEUCYL-LEUCINE ALDEHYDE; DNA BINDING PROTEIN; ERN1 PROTEIN, HUMAN; LEUPEPTIN; PROTEIN SERINE THREONINE KINASE; REGULATORY FACTOR X TRANSCRIPTION FACTOR; RIBONUCLEASE; SMALL INTERFERING RNA; TRANSCRIPTION FACTOR; XBP1 PROTEIN, HUMAN;

APOPTOSIS; ARTICLE; ENDOPLASMIC RETICULUM STRESS; FLOW CYTOMETRY; GENE EXPRESSION; GENE SILENCING; GENETIC TRANSFECTION; MOUTH SQUAMOUS CELL CARCINOMA; PRIORITY JOURNAL; REAL TIME POLYMERASE CHAIN REACTION; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SIGNAL TRANSDUCTION; WESTERN BLOTTING; GENETICS; HUMAN; METABOLISM; MOUTH TUMOR; PHYSIOLOGY; SQUAMOUS CELL CARCINOMA; TUMOR CELL LINE;

APOPTOSIS; CARCINOMA, SQUAMOUS CELL; CELL LINE, TUMOR; DNA-BINDING PROTEINS; ENDOPLASMIC RETICULUM STRESS; ENDORIBONUCLEASES; GENE SILENCING; HUMANS; LEUPEPTINS; MAP KINASE SIGNALING SYSTEM; MOUTH NEOPLASMS; PROTEIN-SERINE-THREONINE KINASES; REGULATORY FACTOR X TRANSCRIPTION FACTORS; RNA, SMALL INTERFERING; SIGNAL TRANSDUCTION; TNF RECEPTOR-ASSOCIATED FACTOR 2; TRANSCRIPTION FACTORS; X-BOX BINDING PROTEIN 1;

EID: 84954524069     PISSN: 07533322     EISSN: 19506007     Source Type: Journal    
DOI: 10.1016/j.biopha.2015.12.010     Document Type: Article

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