Reversal of vinblastine resistance by a new staurosporine derivative, NA-382, in cells
- 1 June 1992
- journal article
- Published by Elsevier in Cancer Letters
- Vol. 64 (2) , 177-183
- https://doi.org/10.1016/0304-3835(92)90079-b
Abstract
No abstract availableKeywords
Funding Information
- Ministry of Education, Culture, Sports, Science and Technology
This publication has 13 references indexed in Scilit:
- Staurosporine, a potent inhibitor of C-kinase, enhances drug accumulation in multidrug-resistant cellsBiochemical and Biophysical Research Communications, 1990
- Circumvention of multidrug resistance in P388 murine leukemia cells by a novel inhibitor of cyclic AMP-dependent protein kinase, H-87Cancer Letters, 1990
- Correlation of protein kinase C translocation, P-glycoprotein phosphorylation and reduced drug accumulation in multidrug resistant human KB cellsBiochemical and Biophysical Research Communications, 1990
- Phosphorylation of the multidrug resistance associated glycoproteinBiochemistry, 1987
- Staurosporine, a potent inhibitor of phospholipidCa++dependent protein kinaseBiochemical and Biophysical Research Communications, 1986
- An inhibitor of protein kinase C, 1-(5-isoquinolinylsulfonyl)-2-methylpiperazine(H-7) inhibits TPA-induced reduction of vincristine uptake from P388 murine leukemic cellLeukemia Research, 1986
- Amplification of P-glycoprotein genes in multidrug-resistant mammalian cell linesNature, 1985
- Detection of P-glycoprotein in multidrug-resistant cell lines by monoclonal antibodiesNature, 1985
- Isolation and genetic characterization of human KB cell lines resistant to multiple drugsSomatic Cell and Molecular Genetics, 1985
- Isoquinolinesulfonamides, novel and potent inhibitors of cyclic nucleotide-dependent protein kinase and protein kinase CBiochemistry, 1984