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Search: onr:"swepub:oai:DiVA.org:uu-94699" > Screening of an ann...

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Screening of an annotated compound library for drug activity in a resistant myeloma cell line

Rickardson, Linda (author)
Uppsala universitet,Klinisk farmakologi,Cancer Pharmacology and Informatics
Fryknäs, Mårten (author)
Uppsala universitet,Institutionen för genetik och patologi,Cancer Pharmacology and Informatics
Haglund, Caroline (author)
Uppsala universitet,Klinisk farmakologi,Cancer Pharmacology and Informatics
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Lövborg, Henrik (author)
Uppsala universitet,Klinisk farmakologi,Cancer Pharmacology and Informatics
Nygren, Peter (author)
Uppsala universitet,Institutionen för onkologi, radiologi och klinisk immunologi,Cancer Pharmacology and Informatics
Gustafsson, Mats (author)
Uppsala universitet,Institutionen för genetik och patologi,Signalbehandling,Cancer Pharmacology and Informatics
Isaksson, Anders (author)
Uppsala universitet,Institutionen för genetik och patologi,Cancer Pharmacology and Informatics
Larsson, Rolf (author)
Uppsala universitet,Klinisk farmakologi,Cancer Pharmacology and Informatics
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 (creator_code:org_t)
2006-03-10
2006
English.
In: Cancer Chemotherapy and Pharmacology. - : Springer Science and Business Media LLC. - 0344-5704 .- 1432-0843. ; 58:6, s. 749-758
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Purpose: Resistance to anticancer drugs is a major problem in chemotherapy. In order to identify drugs with selective cytotoxic activity in drug-resistant cancer cells, the annotated compound library LOPAC(1280), containing compounds from 56 pharmacological classes, was screened in the myeloma cell line RPMI 8226 and its doxorubicin-resistant subline 8226/Dox40. Methods: Cell survival was measured by the Fluorometric Microculture Cytotoxicity Assay. Results: Selective cytotoxic activity in 8226/Dox40 was obtained for 33 compounds, with the most pronounced difference observed for the glucocorticoids. A microarray analysis of the cells showed a difference in mRNA-expression for the glucocorticoid receptor suggesting potential mechanisms for the difference in glucocorticoid sensitivity. In the presence of the glucocorticoid-receptor antagonist RU486, the sensitivity to the glucocorticoids was reduced and a similar effect level in RPMI 8226 and 8226/Dox40 was achieved. Conclusion: In conclusion, screening of mechanistically annotated compounds on drug-resistant cancer cells can identify compounds with selective activity and provide a basis for the development of novel treatments of drug-resistant malignancies.

Keyword

anticancer drug resistance
drug screening
annotated compound library
glucocorticoids
gene expression
MEDICINE
MEDICIN

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