Aouida M~Ramotar D, 2004

Pubmed ID 14871844
Title A genome-wide screen in Saccharomyces cerevisiae reveals altered transport as a mechanism of resistance to the anticancer drug bleomycin.
Authors Mustapha Aouida, Nicolas Pagé, Anick Leduc, Matthias Peter, Dindial Ramotar
Abstract The potent DNA damaging agent bleomycin (BLM) is highly effective for treating various cancers, although, in certain individuals, the development of cellular resistance to the drug can severely diminish its antineoplastic properties. We performed two independent genome-wide screens using a Saccharomyces cerevisiae mutant collection to isolate variants exhibiting either sensitivity or resistance to BLM. This procedure reproducibly identified a relatively large collection of 231 BLM-hypersensitive mutants, representing genes belonging to diverse functional groups. In contrast, only five BLM-resistant mutants could be recovered by our screens. Among these latter mutants, three were deleted for genes involved in plasma membrane transport, including the L-carnitine transporter Agp2, as well as the kinases Ptk2 and Sky1, which are involved in regulating polyamine transport. We further showed that Agp2 acts as a transporter of BLM and that overexpression of this transporter significantly enhances BLM-induced cell killing. Our data strongly implicate membrane transport as a key determinant in BLM resistance in yeast. This finding is critical, given that very little is known about BLM transport in human cells. Indeed, characterization of analogous mechanisms in humans may ultimately lead to enhancement of the antitumor properties of BLM.
Citation Cancer Res. 2004; 64:1102-9

Datasets

Download the list of datasets
Papers Phenotype Conditions Collection Tested mutants Data Details
Aouida M~Ramotar D, 2004 growth (undefined) bleomycin [1-7.5 ug/ml] hap a 4,784 Discrete

Curation history

Data

Feb. 25, 2014 Waiting for tested.
Nov. 21, 2014 Ready to load.
Nov. 21, 2014 Loaded.

Tested strains

Feb. 25, 2014 Request sent.
Nov. 11, 2014 Request sent.
Nov. 21, 2014 Ready to load.
Nov. 21, 2014 Loaded.