Agents that reverse multidrug resistance, tamoxifen, verapamil, and cyclosporin A, block glycosphingolipid metabolism by inhibiting ceramide glycosylation in human cancer cells

Journal of Biological Chemistry

Volumn 272, Issue 3, 1997, Pages 1682-1687

  Lavie, Yaakov ^a   Cao, Hui Ting ^a,b   Volner, Alon ^a   Lucci, Anthony ^a   Han, Tie Yan ^a   Geffen, Vivian ^a   Giuliano, Armando E ^a   Cabot, Myles C ^a  

^a JOHN WAYNE CANCER INSTITUTE   (United States)

^b INSTITUTE OF BIOCHEMISTRY AND CELL BIOLOGY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

CERAMIDE; CYCLOSPORIN A; GLYCOSPHINGOLIPID; TAMOXIFEN; VERAPAMIL;

ARTICLE; CANCER; DRUG EFFECT; DRUG METABOLISM; GLYCOSYLATION; HUMAN; HUMAN CELL; MULTIDRUG RESISTANCE; PRIORITY JOURNAL;

CERAMIDES; CYCLOSPORINE; DOXORUBICIN; DRUG RESISTANCE, MULTIPLE; DRUG RESISTANCE, NEOPLASM; GLYCOSPHINGOLIPIDS; GLYCOSYLATION; HUMANS; MEPERIDINE; TAMOXIFEN; TUMOR CELLS, CULTURED; VERAPAMIL;

MINK CELL FOCUS-FORMING VIRUS;

EID: 0031019309     PISSN: 00219258     EISSN: None     Source Type: Journal    
DOI: 10.1074/jbc.272.3.1682     Document Type: Article

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