Publication:
Triple negative breast cancer: New therapeutic approaches and BRCA status

dc.contributor.authorGüney Eskiler, Gamze
dc.contributor.buuauthorÇeçener, Gülşah
dc.contributor.buuauthorEgeli, Ünal
dc.contributor.buuauthorTunca, Berrin Türkei
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentTıbbi Biyoloji Ana Bilim Dalı
dc.contributor.orcid0000-0002-3820-424X
dc.contributor.orcid0000-0001-7904-883X
dc.contributor.orcid0000-0002-1619-6680
dc.contributor.researcheridAAP-9988-2020
dc.contributor.researcheridAAH-1420-2021
dc.contributor.researcheridABI-6078-2020
dc.contributor.scopusid6508156530
dc.contributor.scopusid55665145000
dc.contributor.scopusid6602965754
dc.date.accessioned2022-12-21T13:49:26Z
dc.date.available2022-12-21T13:49:26Z
dc.date.issued2018-04-25
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.
dc.identifier.citationEskiler, G. G. vd. (2018). ''Triple negative breast cancer: new therapeutic approaches and BRCA status''. APMIS, 126(5), 371-379.
dc.identifier.endpage379
dc.identifier.issn0903-4641
dc.identifier.issn1600-0463
dc.identifier.issue5
dc.identifier.pubmed29696717
dc.identifier.scopus2-s2.0-85045939792
dc.identifier.startpage371
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.identifier.volume126
dc.identifier.wos000430912200002
dc.indexed.scopusScopus
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherWiley
dc.relation.collaborationYurt içi
dc.relation.journalAPMIS
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectTriple negative breast cancer
dc.subjectBRCA1/2
dc.subjectSynthetic lethality
dc.subjectTherapeutic agents
dc.subjectPARP inhibitors
dc.subjectMutation carriers
dc.subjectTargeted therapy
dc.subjectParp inhibitors
dc.subjectTurkish breast
dc.subjectGermline brca1
dc.subjectOvarian
dc.subjectGenes
dc.subjectSusceptibility
dc.subjectManagement
dc.subjectFamilies
dc.subjectImmunology
dc.subjectMicrobiology
dc.subjectPathology
dc.subject.emtreeBRCA1 protein
dc.subject.emtreeBRCA2 protein
dc.subject.emtreeCytokeratin 17
dc.subject.emtreeCytokeratin 5
dc.subject.emtreeCytokeratin 6
dc.subject.emtreeEpidermal growth factor receptor
dc.subject.emtreeNiraparib
dc.subject.emtreeOlaparib
dc.subject.emtreeRucaparib
dc.subject.emtreeTalazoparib
dc.subject.emtreeVeliparib
dc.subject.emtreeNicotinamide adenine dinucleotide adenosine diphosphate ribosyltransferase inhibitor
dc.subject.emtreeCancer growth
dc.subject.emtreeCancer incidence
dc.subject.emtreeCancer patient
dc.subject.emtreeCancer staging
dc.subject.emtreeCancer surgery
dc.subject.emtreeCancer survival
dc.subject.emtreeDisease free survival
dc.subject.emtreeFemale
dc.subject.emtreeGene mutation
dc.subject.emtreeGenetic risk
dc.subject.emtreeGenomic instability
dc.subject.emtreeHuman
dc.subject.emtreeInduced resistance
dc.subject.emtreeMedical history
dc.subject.emtreePrediction
dc.subject.emtreePrevalence
dc.subject.emtreePriority journal
dc.subject.emtreeReview
dc.subject.emtreeTriple negative breast cancer
dc.subject.emtreeGenetics
dc.subject.emtreeTriple negative breast cancer
dc.subject.emtreeTumor suppressor gene
dc.subject.meshFemale
dc.subject.meshGenes, BRCA1
dc.subject.meshGenes, BRCA2
dc.subject.meshHumans
dc.subject.meshPoly(ADP-ribose) polymerase inhibitors
dc.subject.meshTriple negative breast neoplasms
dc.subject.scopusTriple Negative Breast Neoplasms; Negative; Hormone Receptors
dc.subject.wosImmunology
dc.subject.wosMicrobiology
dc.subject.wosPathology
dc.titleTriple negative breast cancer: New therapeutic approaches and BRCA status
dc.typeReview
dc.wos.quartileQ2 (Pathology)
dc.wos.quartileQ3 (Microbiology)
dc.wos.quartileQ4 (Immunology)
dc.wos.quartileQ2
dc.wos.quartileQ3
dc.wos.quartileQ4
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Tıbbi Biyoloji Ana Bilim Dalı
local.indexed.atPubMed
local.indexed.atWOS
local.indexed.atScopus

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