Opposing actions of endocannabinoids on cholangiocarcinoma growth: Recruitment of Fas and Fas ligand to lipid rafts

Journal of Biological Chemistry

Volumn 282, Issue 17, 2007, Pages 13098-13113

  DeMorrow, Sharon ^a   Glaser, Shannon ^a   Francis, Heather ^a   Venter, Julie ^a   Vaculin, Bradley ^a   Vaculin, Shelley ^a   Alpini, Gianfranco ^a,b,c  

^a TEXAS A M COLLEGE OF MEDICINE   (United States)

^b SCOTT AND WHITE MEMORIAL HOSPITAL   (United States)

^c VETERANS AFFAIRS MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMIDES; CELL GROWTH; CELL PROLIFERATION; GLYCEROL; LIGANDS; LIPIDS; TUMORS;

CELL LINES; ENDOCANNABINOIDS; RAFTS;

PROTEINS;

2 ARACHIDONOYLGLYCEROL; ANANDAMIDE; CANNABINOID RECEPTOR; CERAMIDE; ENDOCANNABINOID; FAS ANTIGEN; FAS LIGAND; FLOTILLIN 1; MEMBRANE PROTEIN; METHYL BETA CYCLODEXTRIN; PROTEIN KINASE LYN; 2-ARACHIDONYLGLYCEROL; ACYLGLYCEROL; AMIDE; ANTIINFECTIVE AGENT; ARACHIDONIC ACID DERIVATIVE; BETA CYCLODEXTRIN DERIVATIVE; FILIPIN; FLOTILLINS; INHIBITORY GUANINE NUCLEOTIDE BINDING PROTEIN; LYN PROTEIN-TYROSINE KINASE; METHYL-BETA-CYCLODEXTRIN; PROTEIN TYROSINE KINASE; TUMOR PROTEIN; UNCLASSIFIED DRUG;

ANTINEOPLASTIC ACTIVITY; ARTICLE; BILE DUCT CARCINOMA; BIOACCUMULATION; CANCER GROWTH; CANCER INHIBITION; CELL CYCLE PROGRESSION; CELL GROWTH; CELL MEMBRANE; CELL PROLIFERATION; CONTROLLED STUDY; DRUG EFFECT; HUMAN; HUMAN CELL; LIPID MEMBRANE; LIPID RAFT; MEMBRANE STRUCTURE; MITOSIS INHIBITION; MOLECULAR BIOLOGY; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; DRUG SCREENING; METABOLISM; TUMOR CELL LINE;

ANTI-BACTERIAL AGENTS; ANTIGENS, CD95; ARACHIDONIC ACIDS; BETA-CYCLODEXTRINS; CELL LINE, TUMOR; CELL PROLIFERATION; CHOLANGIOCARCINOMA; DRUG SCREENING ASSAYS, ANTITUMOR; ENDOCANNABINOIDS; FAS LIGAND PROTEIN; FILIPIN; GLYCERIDES; GTP-BINDING PROTEIN ALPHA SUBUNITS, GI-GO; HUMANS; MEMBRANE MICRODOMAINS; MEMBRANE PROTEINS; NEOPLASM PROTEINS; POLYUNSATURATED ALKAMIDES; SRC-FAMILY KINASES;

EID: 34250378332     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M608238200     Document Type: Article

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