Literature DB >> 6744317

High-level, unstable adriamycin resistance in a Chinese hamster mutant cell line with double minute chromosomes.

N Howell, T A Belli, L T Zaczkiewicz, J A Belli.   

Abstract

An Adriamycin-resistant Chinese hamster V79 line was isolated previously in this laboratory. There was about a 5-fold increase in Adriamycin resistance in this mutant as determined from survival curve measurements. Using this low-level Adriamycin-resistant mutant, a cell line with a high level of resistance was isolated after a multistep selection process culminating in continuous growth of the cells in medium containing 5.0 micrograms Adriamycin/ml. These cells are about 3000 times more resistant towards the cytotoxic effects of Adriamycin than is the parental V79 line. This high-level resistance phenotype is unstable and lost upon culture in the absence of drug. The highly resistant cells also showed increased cross-resistance to actinomycin D, Colcemid, and vincristine compared to the low-level resistant cells. Cytogenetic studies showed that these mutant cells contained increased numbers of double minute chromosomes and that the number of double minutes decreased proportionately with the reduction of Adriamycin resistance in cultures changed to drug-free medium. Adriamycin uptake assays demonstrated that there was a further decrease in net uptake relative to the low-level resistant mutant.

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Year:  1984        PMID: 6744317

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


  23 in total

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Authors:  Gregory Young; Luis Reuss; Guillermo A Altenberg
Journal:  Int J Biochem Mol Biol       Date:  2010-06-03

Review 2.  Genetic basis of multidrug resistance of tumor cells.

Authors:  S E Kane; I Pastan; M M Gottesman
Journal:  J Bioenerg Biomembr       Date:  1990-08       Impact factor: 2.945

3.  The three mouse multidrug resistance (mdr) genes are expressed in a tissue-specific manner in normal mouse tissues.

Authors:  J M Croop; M Raymond; D Haber; A Devault; R J Arceci; P Gros; D E Housman
Journal:  Mol Cell Biol       Date:  1989-03       Impact factor: 4.272

4.  Retroviral transfer of a murine cDNA for multidrug resistance confers pleiotropic drug resistance to cells without prior drug selection.

Authors:  B C Guild; R C Mulligan; P Gros; D E Housman
Journal:  Proc Natl Acad Sci U S A       Date:  1988-03       Impact factor: 11.205

5.  Isolation and characterization of DNA sequences amplified in multidrug-resistant hamster cells.

Authors:  P Gros; J Croop; I Roninson; A Varshavsky; D E Housman
Journal:  Proc Natl Acad Sci U S A       Date:  1986-01       Impact factor: 11.205

6.  Chromosome-mediated gene transfer of multidrug resistance.

Authors:  P Gros; D A Fallows; J M Croop; D E Housman
Journal:  Mol Cell Biol       Date:  1986-11       Impact factor: 4.272

7.  Unstable and stable CAD gene amplification: importance of flanking sequences and nuclear environment in gene amplification.

Authors:  J Meinkoth; A M Killary; R E Fournier; G M Wahl
Journal:  Mol Cell Biol       Date:  1987-04       Impact factor: 4.272

8.  The gene encoding multidrug resistance is induced and expressed at high levels during pregnancy in the secretory epithelium of the uterus.

Authors:  R J Arceci; J M Croop; S B Horwitz; D Housman
Journal:  Proc Natl Acad Sci U S A       Date:  1988-06       Impact factor: 11.205

9.  Changes in intra- or extracellular pH do not mediate P-glycoprotein-dependent multidrug resistance.

Authors:  G A Altenberg; G Young; J K Horton; D Glass; J A Belli; L Reuss
Journal:  Proc Natl Acad Sci U S A       Date:  1993-10-15       Impact factor: 11.205

10.  Detection of adriamycin-induced cardiotoxicity in cultured heart cells with technetium 99m-SESTAMIBI.

Authors:  D Piwnica-Worms; M L Chiu; J F Kronauge
Journal:  Cancer Chemother Pharmacol       Date:  1993       Impact factor: 3.333

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