The chemosensitizing potential of GF120918 is independent of the magnitude of P-glycoprotein-mediated resistance to conventional chemotherapeutic agents in a small cell lung cancer line

Oncology Reports

Volumn 6, Issue 1, 1999, Pages 217-218

  Myer, M S ^a   Joone G ^a   Chasen, M R ^a   Van Rensburg, C E J ^a,b  

^a UNIVERSITY OF PRETORIA   (South Africa)

^b Department of Immunology ^*  (South Africa)

Author keywords

GF120918; Multidrug resistance

Indexed keywords

ACRIDINE DERIVATIVE; DAUNORUBICIN; DOCETAXEL; DRUG DERIVATIVE; ELACRIDAR; ETOPOSIDE; GLYCOPROTEIN P; ISOQUINOLINE DERIVATIVE; NAVELBINE; PACLITAXEL; TAXOID; TETRAHYDROISOQUINOLINE DERIVATIVE; TUMOR PROTEIN; VINBLASTINE;

ARTICLE; CELL CULTURE; CELL DIVISION; CHEMICAL STRUCTURE; CHEMISTRY; COMPARATIVE STUDY; DRUG ANTAGONISM; DRUG EFFECT; DRUG RESISTANCE; HUMAN; LUNG TUMOR; METABOLISM; MULTIDRUG RESISTANCE; PATHOLOGY; PHYSIOLOGY; SMALL CELL CARCINOMA;

ACRIDINES; CARCINOMA, SMALL CELL; CELL DIVISION; DAUNORUBICIN; DRUG RESISTANCE, MULTIPLE; DRUG RESISTANCE, NEOPLASM; ETOPOSIDE; HUMANS; ISOQUINOLINES; LUNG NEOPLASMS; MOLECULAR STRUCTURE; NEOPLASM PROTEINS; P-GLYCOPROTEIN; PACLITAXEL; TAXOIDS; TETRAHYDROISOQUINOLINES; TUMOR CELLS, CULTURED; VINBLASTINE;

EID: 0032621404     PISSN: 1021335X     EISSN: None     Source Type: Journal    
DOI: 10.3892/or.6.1.217     Document Type: Article

References (5)

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