Zobrazeno 1 - 10
of 33
pro vyhledávání: '"C S, Morrow"'
Autor:
K. A. Pickin, Ronald A. Fleming, C. S. Morrow, Susan L. Morris-Natschke, Gregory L. Kucera, K. S. Ishaq, Richard L. Alexander
Publikováno v:
Journal of Drug Delivery Science and Technology. 19:31-36
We synthesized thioether phospholipid carrier molecules, conjugated each of them to 1-b-D-arabinofuranosylcytosine (ara-C), and synthesized amido containing phospholipid carriers conjugated to gemcitabine. Changing the alkyl chain at the C1- and C2-p
Publikováno v:
Cancer research. 61(14)
We examined the role of multidrug resistance protein (MRP) 1 (ABCC1) in the emergence of mitoxantrone (MX) cross-resistance in a MCF7 breast cancer cell line selected for resistance to etoposide. The resistant cell line, MCF7/VP, expresses high level
Publikováno v:
The Journal of biological chemistry. 276(11)
We investigated the role of phase II (conjugation) and phase III (efflux) detoxification of the anticancer drugs melphalan (MLP) and chlorambucil (CHB). Although both drugs are substrates of Alpha-class glutathione S-transferases (GST) and the monogl
Publikováno v:
Molecular carcinogenesis. 29(3)
Previous studies in our laboratory have shown that the phase III efflux transporter multidrug-resistance protein (MRP)1 can act synergistically with the phase II conjugating glutathione S-transferases (GST) to confer resistance to the toxicities of s
Publikováno v:
The Journal of biological chemistry. 273(32)
To examine the role of multidrug resistance protein 1 (MRP1) and glutathione S-transferases (GSTs) in cellular resistance to antineoplastic drugs, derivatives of MCF7 breast carcinoma cells were developed that express MRP1 in combination with one of
Publikováno v:
Chemico-biological interactions.
The authors have shown that expression of mGSTM1-1 or hGSTP1-1 in MCF-7 cells protects against DNA alkylation by 4-nitroquinoline-1-oxide (NQO) in an isozyme-specific manner and is commensurate with relative specific activity. Expression of GSTs also
Publikováno v:
The Journal of biological chemistry. 269(14)
We investigated the mechanism of sodium butyrate (NaB)-mediated induction of mdr1 mRNA in parental (wild type) and multidrug-resistant (Ad1000) SW620 colon cancer cell lines. NaB treatment resulted in reversible, time-dependent increases in nuclear r
Publikováno v:
Cancer chemotherapy and biological response modifiers. 15
Publikováno v:
The Journal of biological chemistry. 268(11)
The human mdr1 gene encodes a putative drug efflux pump (P-glycoprotein) whose overexpression is associated with the development of multidrug resistance (MDR). The promoter and 5'-flanking DNA of this gene were isolated from a human genomic DNA libra
Publikováno v:
The Journal of biological chemistry. 268(8)
Basal transcription of the human multidrug resistance (mdr1) promoter was studied by chloramphenicol acetyltransferase (CAT) reporter fusion gene analysis in two parental and doxorubicin-resistant human tumor cell lines. Deletion of mdr1 DNA sequence