Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/30022
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dc.contributor.authorGüney Eskiler, Gamze-
dc.date.accessioned2022-12-21T13:49:26Z-
dc.date.available2022-12-21T13:49:26Z-
dc.date.issued2018-04-25-
dc.identifier.citationEskiler, G. G. vd. (2018). ''Triple negative breast cancer: new therapeutic approaches and BRCA status''. APMIS, 126(5), 371-379.en_US
dc.identifier.issn0903-4641-
dc.identifier.issn1600-0463-
dc.identifier.urihttps://doi.org/10.1111/apm.12836-
dc.identifier.urionlinelibrary.wiley.com/doi/10.1111/apm.12836-
dc.identifier.urihttp://hdl.handle.net/11452/30022-
dc.description.abstractTreatment of triple negative breast cancer (TNBC) is a clinically challenging problem due to intriguing clinical and pathologic features of TNBC and natural or induced resistance to existing therapies. However, a great understanding of features of TNBC particularly associated with BRCA mutations has led to the development of different therapeutic approaches. Besides, identification of TNBC subtypes contribute to investigation of the underlying molecular differences and development of new strategies for the treatment of TNBC patients. In this review, we discussed the definition and characteristic properties of TNBC. We summarized an up-to-date description of the reported clinical trials of novel targeted strategies especially PARP inhibitors (PARPi) due to novel and highly potent for the treatment of TNBC. Additionally, we reviewed published studies which investigated the prevalence and types of BRCA1/2 mutation in breast cancer patients to assess and draw attention of association of BRCA status with TNBC. Consequently, the definition subtype of TNBC has important predictive value for the development of new therapeutic agents in the treatment of TNBC. Additionally, the incidence and types of mutations in BRCA-related pathways may be affected by ethnic origin and contribute to the risk of developing TNBC.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectTriple negative breast canceren_US
dc.subjectBRCA1/2en_US
dc.subjectSynthetic lethalityen_US
dc.subjectTherapeutic agentsen_US
dc.subjectPARP inhibitorsen_US
dc.subjectMutation carriersen_US
dc.subjectTargeted therapyen_US
dc.subjectParp inhibitorsen_US
dc.subjectTurkish breasten_US
dc.subjectGermline brca1en_US
dc.subjectOvarianen_US
dc.subjectGenesen_US
dc.subjectSusceptibilityen_US
dc.subjectManagementen_US
dc.subjectFamiliesen_US
dc.subjectImmunologyen_US
dc.subjectMicrobiologyen_US
dc.subjectPathologyen_US
dc.subject.meshFemaleen_US
dc.subject.meshGenes, BRCA1en_US
dc.subject.meshGenes, BRCA2en_US
dc.subject.meshHumansen_US
dc.subject.meshPoly(ADP-ribose) polymerase inhibitorsen_US
dc.subject.meshTriple negative breast neoplasmsen_US
dc.titleTriple negative breast cancer: New therapeutic approaches and BRCA statusen_US
dc.typeReviewen_US
dc.identifier.wos000430912200002tr_TR
dc.identifier.scopus2-s2.0-85045939792tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Tıbbi Biyoloji Anabilim Dalı.tr_TR
dc.contributor.orcid0000-0002-3820-424Xtr_TR
dc.contributor.orcid0000-0001-7904-883Xtr_TR
dc.contributor.orcid0000-0002-1619-6680tr_TR
dc.identifier.startpage371tr_TR
dc.identifier.endpage379tr_TR
dc.identifier.volume126tr_TR
dc.identifier.issue5tr_TR
dc.relation.journalAPMISen_US
dc.contributor.buuauthorÇeçener, Gülşah-
dc.contributor.buuauthorEgeli, Ünal-
dc.contributor.buuauthorTunca, Berrin Türkei-
dc.contributor.researcheridAAP-9988-2020tr_TR
dc.contributor.researcheridAAH-1420-2021tr_TR
dc.contributor.researcheridABI-6078-2020tr_TR
dc.relation.collaborationYurt içitr_TR
dc.identifier.pubmed29696717tr_TR
dc.subject.wosImmunologyen_US
dc.subject.wosMicrobiologyen_US
dc.subject.wosPathologyen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubMeden_US
dc.wos.quartileQ2 (Pathology)en_US
dc.wos.quartileQ3 (Microbiology)en_US
dc.wos.quartileQ4 (Immunology)en_US
dc.contributor.scopusid6508156530tr_TR
dc.contributor.scopusid55665145000tr_TR
dc.contributor.scopusid6602965754tr_TR
dc.subject.scopusTriple Negative Breast Neoplasms; Negative; Hormone Receptorsen_US
dc.subject.emtreeBRCA1 proteinen_US
dc.subject.emtreeBRCA2 proteinen_US
dc.subject.emtreeCytokeratin 17en_US
dc.subject.emtreeCytokeratin 5en_US
dc.subject.emtreeCytokeratin 6en_US
dc.subject.emtreeEpidermal growth factor receptoren_US
dc.subject.emtreeNirapariben_US
dc.subject.emtreeOlapariben_US
dc.subject.emtreeRucapariben_US
dc.subject.emtreeTalazopariben_US
dc.subject.emtreeVelipariben_US
dc.subject.emtreeNicotinamide adenine dinucleotide adenosine diphosphate ribosyltransferase inhibitoren_US
dc.subject.emtreeCancer growthen_US
dc.subject.emtreeCancer incidenceen_US
dc.subject.emtreeCancer patienten_US
dc.subject.emtreeCancer stagingen_US
dc.subject.emtreeCancer surgeryen_US
dc.subject.emtreeCancer survivalen_US
dc.subject.emtreeDisease free survivalen_US
dc.subject.emtreeFemaleen_US
dc.subject.emtreeGene mutationen_US
dc.subject.emtreeGenetic risken_US
dc.subject.emtreeGenomic instabilityen_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeInduced resistanceen_US
dc.subject.emtreeMedical historyen_US
dc.subject.emtreePredictionen_US
dc.subject.emtreePrevalenceen_US
dc.subject.emtreePriority journalen_US
dc.subject.emtreeReviewen_US
dc.subject.emtreeTriple negative breast canceren_US
dc.subject.emtreeGeneticsen_US
dc.subject.emtreeTriple negative breast canceren_US
dc.subject.emtreeTumor suppressor geneen_US
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