1α,25-dihydroxyvitamin D3 inhibits programmed cell death in HL-60 cells by activation of sphingosine kinase

Cancer Research

Volumn 58, Issue 9, 1998, Pages 1817-1824

  Kleuser, Burkhard ^a   Cuvillier, Olivier ^a   Spiegel, Sarah ^a  

^a GEORGETOWN UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CERAMIDE; CHELERYTHRINE; DIHYDROXYCOLECALCIFEROL; PHORBOL 13 ACETATE 12 MYRISTATE; PHOSPHOTRANSFERASE; RETINOIC ACID; RETINOIC ACID RECEPTOR; SPHINGOMYELIN PHOSPHODIESTERASE; SPHINGOSINE 1 PHOSPHATE; ALKALOID; BENZOPHENANTHRIDINE DERIVATIVE; CALCITRIOL; CARCINOGEN; DRUG DERIVATIVE; ENZYME INHIBITOR; LYSOPHOSPHOLIPID; N,N DIMETHYLSPHINGOSINE; N,N-DIMETHYLSPHINGOSINE; PHENANTHRIDINE DERIVATIVE; SPHINGOSINE; SPHINGOSINE 1-PHOSPHATE; SPHINGOSINE KINASE;

APOPTOSIS; ARTICLE; CANCER INHIBITION; CELL PROTECTION; CELL STRAIN HL 60; CELL SURVIVAL; COMPETITIVE INHIBITION; DOSE RESPONSE; DOSE TIME EFFECT RELATION; DRUG ACTIVITY; DRUG MECHANISM; HUMAN; HUMAN CELL; PRIORITY JOURNAL; PROMYELOCYTIC LEUKEMIA; SECOND MESSENGER; DRUG ANTAGONISM; DRUG EFFECT; ENZYMOLOGY; METABOLISM; PATHOLOGY; TIME;

ALKALOIDS; APOPTOSIS; BENZOPHENANTHRIDINES; CALCITRIOL; CARCINOGENS; CELL SURVIVAL; CERAMIDES; DOSE-RESPONSE RELATIONSHIP, DRUG; ENZYME INHIBITORS; HL-60 CELLS; HUMANS; LYSOPHOSPHOLIPIDS; PHENANTHRIDINES; PHOSPHOTRANSFERASES (ALCOHOL GROUP ACCEPTOR); SPHINGOSINE; TETRADECANOYLPHORBOL ACETATE; TIME FACTORS;

EID: 0032056362     PISSN: 00085472     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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