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                  <mods:namePart>Perez, Marco</mods:namePart>
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                  <mods:namePart>Peinado-Serrano, Javier</mods:namePart>
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                  <mods:namePart>Tous, Cristina</mods:namePart>
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                  <mods:namePart>Martin-Broto, Javier</mods:namePart>
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                  <mods:namePart>Carnero, Amancio</mods:namePart>
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                  <mods:namePart>Garcia-Heredia, Jose Manuel</mods:namePart>
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                  <mods:namePart>Felipe-Abrio, Irene</mods:namePart>
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                  <mods:namePart>Tous, Cristina</mods:namePart>
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                  <mods:namePart>Ferrer, Irene</mods:namePart>
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                  <mods:namePart>Martin-Broto, Javier</mods:namePart>
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               <mods:name>
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                  <mods:namePart>Saez, Carmen</mods:namePart>
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               <mods:name>
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                  <mods:namePart>Carnero, Amancio</mods:namePart>
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                  <mods:dateAccessioned encoding="iso8601">2024-10-23T09:08:08Z</mods:dateAccessioned>
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                  <mods:dateIssued encoding="iso8601">2016</mods:dateIssued>
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               <mods:identifier type="doi">10.18632/oncotarget.11475</mods:identifier>
               <mods:identifier type="e-issn">1949-2553</mods:identifier>
               <mods:identifier type="journal">Oncotarget</mods:identifier>
               <mods:identifier type="other">http://hdl.handle.net/10668/10392</mods:identifier>
               <mods:identifier type="pubmedID">27563810</mods:identifier>
               <mods:identifier type="uri">https://hdl.handle.net/20.500.12105/25210</mods:identifier>
               <mods:abstract>Sarcomas are malignant tumors accounting for a high percentage of cancer morbidity and mortality in children and young adults. Surgery and radiation therapy are the accepted treatments for most sarcomas; however, patients with metastatic disease are treated with systemic chemotherapy. Many tumors display marginal levels of chemoresponsiveness, and new treatment approaches are needed. MAP17 is a small non-glycosylated membrane protein overexpressed in carcinomas. The levels of MAP17 could be used as a prognostic marker to predict the response to bortezomib in hematological malignancies and in breast tumors. Therefore, we analyzed the expression of this oncogene in sarcomas and its relationship with clinico-pathological features, as well as tested whether it can be used as a new biomarker to predict the therapeutic response to bortezomib and new therapies for sarcomas. We found that the levels of MAP17 were related to clinical features and poor survival in a cohort of 69 patients with different sarcoma types, not being restricted to any special subtype of tumor. MAP17 expression is associated with poor overall survival (p</mods:abstract>
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               <mods:subject>
                  <mods:topic>MAP17</mods:topic>
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               <mods:subject>
                  <mods:topic>Biomarker</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Bortezomib</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Sarcomas</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>PDX</mods:topic>
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               <mods:titleInfo>
                  <mods:title>Efficacy of bortezomib in sarcomas with high levels of MAP17 (PDZK1IP1)</mods:title>
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