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                  <mods:namePart>Sánchez-Muñoz, Alfonso</mods:namePart>
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                  <mods:namePart>Gallego-Domínguez, Elena María</mods:namePart>
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                  <mods:namePart>De Luque, Vanessa</mods:namePart>
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                  <mods:namePart>Ribelles, Nuria</mods:namePart>
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                  <mods:namePart>Lozano-Castro, José</mods:namePart>
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                  <mods:namePart>Alba-Conejo, Emilio</mods:namePart>
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                  <mods:dateAccessioned encoding="iso8601">2024-01-31T18:37:53Z</mods:dateAccessioned>
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               <mods:identifier type="citation">Sánchez-Muñoz A, Gallego E, de Luque V, Pérez-Rivas LG, Vicioso L, Ribelles N, Lozano J, Alba E. Lack of evidence for KRAS oncogenic mutations in triple-negative breast cancer. BMC Cancer. 2010 Apr 13;10:136. doi: 10.1186/1471-2407-10-136. PMID: 20385028; PMCID: PMC2868051.</mods:identifier>
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               <mods:identifier type="doi">10.1186/1471-2407-10-136</mods:identifier>
               <mods:abstract>Background: Mutational analysis of the KRAS gene has recently been established as a complementary in vitro diagnostic tool for the identification of patients with colorectal cancer who will not benefit from anti-epidermal growth factor receptor (EGFR) therapies. Assessment of the mutation status of KRAS might also be of potential relevance in other EGFR-overexpressing tumors,&#xd;
such as those occurring in breast cancer. Although KRAS is mutated in only a minor fraction of breast tumors (5%), about 60% of the basal-like subtype express EGFR and, therefore could be targeted by EGFR inhibitors. We aimed to study the mutation frequency of KRAS in that subtype of breast tumors to provide a molecular basis for the evaluation of anti-EGFR therapies.&#xd;
Methods: Total, genomic DNA was obtained from a group of 35 formalin-fixed paraffin-embedded, triple-negative breast tumor samples. Among these, 77.1% (27/35) were defined as basal-like by immunostaining specific for the established surrogate markers cytokeratin (CK) 5/6 and/or EGFR. KRAS mutational status was determined in the purified DNA samples by Real Time&#xd;
(RT)-PCR using primers specific for the detection of wild-type KRAS or the following seven oncogenic somatic mutations: Gly12Ala, Gly12Asp, Gly12Arg, Gly12Cys, Gly12Ser, Gly12Val and Gly13Asp.&#xd;
Results: We found no evidence of KRAS oncogenic mutations in all analyzed tumors.&#xd;
Conclusions: This study indicates that KRAS mutations are very infrequent in triple-negative breast tumors and that EGFR inhibitors may be of potential benefit in the treatment of basal-like breast tumors, which overexpress EGFR in&#xd;
about 60% of all cases.</mods:abstract>
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               <mods:accessCondition type="useAndReproduction">Atribución 4.0 Internacional</mods:accessCondition>
               <mods:subject>
                  <mods:topic>Cáncer - Aspectos genéticos</mods:topic>
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               <mods:subject>
                  <mods:topic>Mamas - Cáncer - Aspectos genéticos</mods:topic>
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                  <mods:title>Lack of evidence for KRAS oncogenic mutations in triple-negative breast cancer.</mods:title>
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