Εμφάνιση απλής εγγραφής

dc.creatorDimitrakopoulos F.-I., Kottorou A., Tzezou A.en
dc.date.accessioned2023-01-31T07:55:58Z
dc.date.available2023-01-31T07:55:58Z
dc.date.issued2021
dc.identifier10.1016/j.canlet.2021.05.030
dc.identifier.issn03043835
dc.identifier.urihttp://hdl.handle.net/11615/73322
dc.description.abstractDespite the enormous advances during the last three decades, breast cancer continues to be the most frequent type of cancer as well as one of the most frequent cancer-related causes of death in women. Therapeutic management of patients with hormone receptor-positive breast cancer becomes very often a challenge, since de novo or acquired resistance deprives a significant percentage of the patients from the clinical benefit of the well-tolerated hormone therapy. Several molecular mechanisms are implicated in resistance to endocrine therapy, including changes in hormone receptor signaling, activation of parallel signaling pathways, modifications of cell cycle regulators, activation of different transcription factors as well as changes in stem cells activity. In addition, a growing number of studies supports the pivotal role of epigenetic changes not only in the initiation and progression of breast cancer, but also in resistance to endocrine therapy. These changes refer to DNA methylation, histone post-translational modifications as well as to ncRNAs alterations. In this review, we provide an overview of epigenetic mechanisms underlying the endocrine resistance focusing exclusively on breast cancer patients. © 2021 Elsevier B.V.en
dc.language.isoenen
dc.sourceCancer Lettersen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85107790149&doi=10.1016%2fj.canlet.2021.05.030&partnerID=40&md5=f29f6ae07c179af9b27b781e031fd692
dc.subjectafimoxifeneen
dc.subjectanacardic aciden
dc.subjectandrogenen
dc.subjectaromataseen
dc.subjectaromatase inhibitoren
dc.subjectazacitidineen
dc.subjectbeclin 1en
dc.subjectbeta cateninen
dc.subjectcholesterolen
dc.subjectcircular ribonucleic aciden
dc.subjectcomplementary DNAen
dc.subjectcyclin D1en
dc.subjectcyclin dependent kinase inhibitor 1Ben
dc.subjectcytochrome P450 2D6en
dc.subjectdipyridamoleen
dc.subjectDNA methyltransferaseen
dc.subjectentinostaten
dc.subjectepidermal growth factor receptor 2en
dc.subjectestradiolen
dc.subjectestriolen
dc.subjectestrogen receptoren
dc.subjectestrogen receptor alphaen
dc.subjectestrogen receptor betaen
dc.subjectestroneen
dc.subjectexemestaneen
dc.subjectfollitropinen
dc.subjectfulvestranten
dc.subjectgonadotropinen
dc.subjecthistone acetyltransferaseen
dc.subjecthistone deacetylaseen
dc.subjecthistone lysine methyltransferaseen
dc.subjecthistone methyltransferaseen
dc.subjecthomeodomain proteinen
dc.subjectinterleukin 1betaen
dc.subjectinterleukin 6en
dc.subjectJanus kinaseen
dc.subjectlong untranslated RNAen
dc.subjectlow density lipoprotein receptor related protein 6en
dc.subjectluteinizing hormoneen
dc.subjectmammalian target of rapamycinen
dc.subjectmessenger RNAen
dc.subjectmicroRNA 221en
dc.subjectmicroRNA 222en
dc.subjectmitogen activated protein kinaseen
dc.subjectNotch receptoren
dc.subjectphosphatidylinositol 3 kinaseen
dc.subjectprogesterone receptoren
dc.subjectprotein kinase Ben
dc.subjectprotein p53en
dc.subjectprotein tyrosine kinaseen
dc.subjectraloxifeneen
dc.subjectreceptor interacting protein 140en
dc.subjectRNA polymerase IIen
dc.subjectselective estrogen receptor modulatoren
dc.subjectSTAT proteinen
dc.subjecttamoxifenen
dc.subjectthrombospondin 1en
dc.subjecttoremifeneen
dc.subjecttranscription factoren
dc.subjecttranscription factor GATA 3en
dc.subjecttranscription factor YY1en
dc.subjecttransforming growth factor beta receptoren
dc.subjecttucidinostaten
dc.subjectubiquitinen
dc.subjectuntranslated RNAen
dc.subjectWnt11 proteinen
dc.subjectestrogen receptoren
dc.subjectadipose tissueen
dc.subjectAkt/mTOR signalingen
dc.subjectapoptosisen
dc.subjectbone densityen
dc.subjectbreast cancer cell lineen
dc.subjectcancer associated fibroblasten
dc.subjectcancer cellen
dc.subjectcancer growthen
dc.subjectcancer mortalityen
dc.subjectcarcinogenesisen
dc.subjectcause of deathen
dc.subjectcell cycleen
dc.subjectcell proliferationen
dc.subjectcholesterol blood levelen
dc.subjectchromatinen
dc.subjectCpG islanden
dc.subjectdisease exacerbationen
dc.subjectDNA methylationen
dc.subjectDown syndromeen
dc.subjectendocrine glanden
dc.subjectendometrium canceren
dc.subjectepigeneticsen
dc.subjectestrogen receptor positive breast canceren
dc.subjectestrogen responsive elementen
dc.subjectestrogen signalingen
dc.subjectgene expressionen
dc.subjectgene mutationen
dc.subjectgrowth regulationen
dc.subjecthistone modificationen
dc.subjecthormonal therapyen
dc.subjecthormone resistanceen
dc.subjecthypothalamus hypophysis systemen
dc.subjecthypoxiaen
dc.subjectJAK-STAT signalingen
dc.subjectluminal A breast canceren
dc.subjectluminal B breast canceren
dc.subjectmammary glanden
dc.subjectMAPK signalingen
dc.subjectMCF-7 cell lineen
dc.subjectMDA-MB-231 cell lineen
dc.subjectmenstruationen
dc.subjectnonhumanen
dc.subjectNotch signalingen
dc.subjectorganogenesisen
dc.subjectovariectomyen
dc.subjectovary canceren
dc.subjectoverall survivalen
dc.subjectPi3K/Akt signalingen
dc.subjectpostmenopauseen
dc.subjectprogression free survivalen
dc.subjectpromoter regionen
dc.subjectquality of lifeen
dc.subjectShort Surveyen
dc.subjectsignal transductionen
dc.subjectSK-BR-3 cell lineen
dc.subjectsystematic reviewen
dc.subjectTGF beta signalingen
dc.subjectanimalen
dc.subjectbreast tumoren
dc.subjectfemaleen
dc.subjectgenetic epigenesisen
dc.subjectgeneticsen
dc.subjecthumanen
dc.subjectmetabolismen
dc.subjectprotein processingen
dc.subjectAnimalsen
dc.subjectBreast Neoplasmsen
dc.subjectDNA Methylationen
dc.subjectEpigenesis, Geneticen
dc.subjectFemaleen
dc.subjectHumansen
dc.subjectProtein Processing, Post-Translationalen
dc.subjectReceptors, Estrogenen
dc.subjectSignal Transductionen
dc.subjectElsevier Ireland Ltden
dc.titleEndocrine resistance and epigenetic reprogramming in estrogen receptor positive breast canceren
dc.typeotheren


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