Publication:
Efficacy of bortezomib in sarcomas with high levels of MAP17 (PDZK1IP1).

dc.contributor.authorPerez, Marco
dc.contributor.authorPeinado-Serrano, Javier
dc.contributor.authorGarcia-Heredia, Jose Manuel
dc.contributor.authorFelipe-Abrio, Irene
dc.contributor.authorTous, Cristina
dc.contributor.authorFerrer, Irene
dc.contributor.authorMartin-Broto, Javier
dc.contributor.authorSaez, Carmen
dc.contributor.authorCarnero, Amancio
dc.date.accessioned2023-01-25T08:35:54Z
dc.date.available2023-01-25T08:35:54Z
dc.date.issued2016
dc.description.abstractSarcomas 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
dc.identifier.doi10.18632/oncotarget.11475
dc.identifier.essn1949-2553
dc.identifier.pmcPMC5341855
dc.identifier.pmid27563810
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5341855/pdf
dc.identifier.unpaywallURLhttp://www.oncotarget.com/index.php?journal=oncotarget&page=article&op=download&path%5B%5D=11475&path%5B%5D=48021
dc.identifier.urihttp://hdl.handle.net/10668/10392
dc.issue.number41
dc.journal.titleOncotarget
dc.journal.titleabbreviationOncotarget
dc.language.isoen
dc.organizationIBIS
dc.page.number67033-67046
dc.pubmedtypeJournal Article
dc.rightsAttribution 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectMAP17
dc.subjectbiomarker
dc.subjectbortezomib
dc.subjectsarcomas
dc.subjectPDX
dc.subject.meshAdolescent
dc.subject.meshAdult
dc.subject.meshAged
dc.subject.meshAnimals
dc.subject.meshAntineoplastic Agents
dc.subject.meshArea Under Curve
dc.subject.meshBiomarkers, Tumor
dc.subject.meshBortezomib
dc.subject.meshDisease-Free Survival
dc.subject.meshFemale
dc.subject.meshHumans
dc.subject.meshKaplan-Meier Estimate
dc.subject.meshMale
dc.subject.meshMembrane Proteins
dc.subject.meshMice
dc.subject.meshMiddle Aged
dc.subject.meshPrognosis
dc.subject.meshROC Curve
dc.subject.meshSarcoma
dc.subject.meshSensitivity and Specificity
dc.subject.meshXenograft Model Antitumor Assays
dc.subject.meshYoung Adult
dc.titleEfficacy of bortezomib in sarcomas with high levels of MAP17 (PDZK1IP1).
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number7
dspace.entity.typePublication

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