dc.creatorVargas-Rondón, Natalia
dc.creatorVillegas, Victoria E.
dc.creatorRondón-Lagos, Milena
dc.date.accessioned2020-03-31T20:48:34Z
dc.date.accessioned2022-09-22T14:03:10Z
dc.date.available2020-03-31T20:48:34Z
dc.date.available2022-09-22T14:03:10Z
dc.date.created2020-03-31T20:48:34Z
dc.date.issued2018
dc.identifier2072-6694
dc.identifierhttps://repository.urosario.edu.co/handle/10336/21328
dc.identifierhttps://doi.org/10.3390/cancers10010004
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3435357
dc.description.abstractCancer is one of the leading causes of death, and despite increased research in recent years, control of advanced-stage disease and optimal therapeutic responses remain elusive. Recent technological improvements have increased our understanding of human cancer as a heterogeneous disease. For instance, four hallmarks of cancer have recently been included, which in addition to being involved in cancer development, could be involved in therapeutic responses and resistance. One of these hallmarks is chromosome instability (CIN), a source of genetic variation in either altered chromosome number or structure. CIN has become a hot topic in recent years, not only for its implications in cancer diagnostics and prognostics, but also for its role in therapeutic responses. Chromosomal alterations are mainly used to determine genetic heterogeneity in tumors, but CIN could also reveal treatment efficacy, as many therapies are based on increasing CIN, which causes aberrant cells to undergo apoptosis. However, it should be noted that contradictory findings on the implications of CIN for the therapeutic response have been reported, with some studies associating high CIN with a better therapeutic response and others associating it with therapeutic resistance. Considering these observations, it is necessary to increase our understanding of the role CIN plays not only in tumor development, but also in therapeutic responses. This review focuses on recent studies that suggest possible mechanisms and consequences of CIN in different disease types, with a primary focus on cancer outcomes and therapeutic responses. © 2018 by the authors. Licensee MDPI, Basel, Switzerland.
dc.languageeng
dc.relationCancers, ISSN:2072-6694, Vol. 10 (2018)
dc.relationhttps://www.mdpi.com/2072-6694/10/1/4
dc.relationCancers
dc.relationVol. 10
dc.rightsinfo:eu-repo/semantics/openAccess
dc.rightsAbierto (Texto Completo)
dc.sourceNicholson, J.M., Cimini, D., Cancer karyotypes: Survival of the fittest (2013) Front. Oncol, 3, p. 148. , [CrossRef] [PubMed]
dc.sourceinstname:Universidad del Rosario
dc.sourcereponame:Repositorio Institucional EdocUR
dc.subjectEpidermal Growth Factor Receptor 2
dc.subjectEstrogen Receptor
dc.subjectSmad2 Protein
dc.subjectSmad4 Protein
dc.subjectAcute Lymphoblastic Leukemia
dc.subjectAneuploidy
dc.subjectBladder Cancer
dc.subjectBreast Cancer
dc.subjectCancer Diagnosis
dc.subjectCancer Growth
dc.subjectCancer Prognosis
dc.subjectCancer Therapy
dc.subjectChromosomal Instability
dc.subjectChromosome Aberration
dc.subjectChromosome Segregation
dc.subjectColorectal Cancer
dc.subjectEndometrium Cancer
dc.subjectGene Function
dc.subjectGene Interaction
dc.subjectGene Mutation
dc.subjectGenetic Heterogeneity
dc.subjectGenetic Variation
dc.subjectHigh Hyperdiploid Acute Lymphoblastic Leukemia
dc.subjectHuman
dc.subjectMalignant Neoplasm
dc.subjectMultiple Myeloma
dc.subjectNon Recurrent Chromosomal Alteration
dc.subjectNonhuman
dc.subjectProstate Cancer
dc.subjectReview
dc.subjectTherapy Resistance
dc.subjectTreatment Outcome
dc.subjectTreatment Response
dc.subjectTumor Growth
dc.subjectUterine Cervix Cancer
dc.subjectFactor de Crecimiento Epidérmico Receptor 2
dc.subjectReceptor de estrógenos
dc.subjectLa proteína Smad2
dc.subjectLa proteína smad4
dc.titleThe role of chromosomal instability in cancer and therapeutic responses
dc.typereview


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