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                  <mods:namePart>Toledo, Luis I</mods:namePart>
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                  <mods:namePart>Murga, Matilde</mods:namePart>
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                  <mods:namePart>Zur, Rafal</mods:namePart>
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                  <mods:namePart>Rodriguez, Antonio</mods:namePart>
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                  <mods:namePart>Martinez, Sonia</mods:namePart>
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                  <mods:namePart>Oyarzabal, Julen</mods:namePart>
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                  <mods:namePart>Pastor, Joaquin</mods:namePart>
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                  <mods:namePart>Bischoff, James R</mods:namePart>
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                  <mods:namePart>Fundación Pfizer</mods:namePart>
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               <mods:name>
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                     <mods:roleTerm type="text">funder</mods:roleTerm>
                  </mods:role>
                  <mods:namePart>Instituto de Salud Carlos III</mods:namePart>
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               <mods:name>
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                     <mods:roleTerm type="text">funder</mods:roleTerm>
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                  <mods:namePart>Ministerio de Ciencia (España)</mods:namePart>
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                  <mods:dateAccessioned encoding="iso8601">2024-02-09T10:13:56Z</mods:dateAccessioned>
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                  <mods:dateIssued encoding="iso8601">2011-06</mods:dateIssued>
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               <mods:identifier type="citation">Nat Struct Mol Biol  . 2011;18(6):721-7</mods:identifier>
               <mods:identifier type="doi">10.1038/nsmb.2076</mods:identifier>
               <mods:identifier type="e-issn">1545-9985</mods:identifier>
               <mods:identifier type="journal">Nature structural &amp; molecular biology</mods:identifier>
               <mods:identifier type="pmc">https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4869831/</mods:identifier>
               <mods:identifier type="pubmedID">21552262</mods:identifier>
               <mods:identifier type="uri">http://hdl.handle.net/20.500.12105/17684</mods:identifier>
               <mods:abstract>Oncogene activation has been shown to generate replication-born DNA damage, also known as replicative stress. The primary responder to replicative stress is not Ataxia-Telangiectasia Mutated (ATM) but rather the kinase ATM and Rad3-related (ATR). One limitation for the study of ATR is the lack of potent inhibitors. We here describe a cell-based screening strategy that has allowed us to identify compounds with ATR inhibitory activity in the nanomolar range. Pharmacological inhibition of ATR generates replicative stress, leading to chromosomal breakage in the presence of conditions that stall replication forks. Moreover, ATR inhibition is particularly toxic for p53-deficient cells, this toxicity being exacerbated by replicative stress-generating conditions such as the overexpression of cyclin E. Notably, one of the compounds we identified is NVP-BEZ235, a dual phosphatidylinositol-3-OH kinase (PI3K) and mTOR inhibitor that is being tested for cancer chemotherapy but that we now show is also very potent against ATM, ATR and the catalytic subunit of DNA-dependent protein kinase (DNA-PKcs).</mods:abstract>
               <mods:language>
                  <mods:languageTerm authority="rfc3066">eng</mods:languageTerm>
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                  <mods:title>A cell-based screen identifies ATR inhibitors with synthetic lethal properties for cancer-associated mutations.</mods:title>
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               <mods:genre>journal article</mods:genre>
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