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dc.rights.licenseopenen_US
hal.structure.identifierInstitut de Neurosciences cognitives et intégratives d'Aquitaine [INCIA]
dc.contributor.authorMORGAT, Clement
dc.contributor.authorBROUSTE, Veronique
hal.structure.identifierInstitut de Neurosciences cognitives et intégratives d'Aquitaine [INCIA]
dc.contributor.authorCHASTEL, Adrien
hal.structure.identifierActions for OnCogenesis understanding and Target Identification in ONcology [ACTION]
dc.contributor.authorVELASCO, Valerie
hal.structure.identifierActions for OnCogenesis understanding and Target Identification in ONcology [ACTION]
dc.contributor.authorMACGROGAN, Gaetan
hal.structure.identifierInstitut de Neurosciences cognitives et intégratives d'Aquitaine [INCIA]
dc.contributor.authorHINDIE, Elif
dc.date.accessioned2023-06-28T12:31:06Z
dc.date.available2023-06-28T12:31:06Z
dc.date.issued2021-12-01
dc.identifier.issn1573-7217en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/183230
dc.description.abstractEnNeurotensin receptor-1 (NTS) is increasingly recognized as a potential target in diverse tumors including breast cancer, but factors associated with NTS expression have not been fully clarified. We studied NTS expression using the Tissue MicroArray (TMA) of primary breast tumors from Institut Bergonié. We also studied association between NTS expression and clinical, pathological, and biological parameters, as well as patient outcomes. Out of 1419 primary breast tumors, moderate to strong positivity for NTS (≥ 10% of tumoral cells stained) was seen in 459 samples (32.4%). NTS staining was cytoplasmic in 304 tumors and nuclear in 155 tumors, a distribution which appeared mutually exclusive. Cytoplasmic overexpression of NTS was present in 21.5% of all breast tumors. In multivariate analysis, factors associated with cytoplasmic overexpression of NTS in breast cancer samples were higher tumor grade, Ki67 ≥ 20%, and higher pT stage. Cytoplasmic NTS was more frequent in tumors other than luminal A (30% versus 17.3%; p < 0.0001). Contrastingly, the main "correlates" of a nuclear location of NTS were estrogen receptor (ER) positivity, low E&E (Elston and Ellis) grade, Ki67 < 20%, and lower pT stage. In NTS-positive samples, cytoplasmic expression of NTS was associated with shorter 10-year metastasis-free interval (p = 0.033) compared to NTS nuclear staining. Ancillary analysis showed NTS expression in 73% of invaded lymph nodes from NTS-positive primaries. NTS overexpression was found in about one-third of breast tumors from patients undergoing primary surgery with two distinct patterns of distribution, cytoplasmic distribution being more frequent in aggressive subtypes. These findings encourage the development of NTS-targeting strategy, including radiopharmaceuticals for imaging and therapy.
dc.description.sponsorshipTranslational Research and Advanced Imaging Laboratory - ANR-10-LABX-0057en_US
dc.language.isoENen_US
dc.subject.enBiological Factors
dc.subject.enBreast Neoplasms
dc.subject.enCell Line
dc.subject.enTumor
dc.subject.enFemale
dc.subject.enHumans
dc.subject.enRadiopharmaceuticals
dc.subject.enReceptors
dc.subject.enNeurotensin
dc.title.enExpression of neurotensin receptor-1 (NTS1) in primary breast tumors, cellular distribution, and association with clinical and biological factors
dc.title.alternativeBreast Cancer Res Treaten_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1007/s10549-021-06402-5en_US
dc.subject.halSciences du Vivant [q-bio]/Neurosciences [q-bio.NC]en_US
dc.identifier.pubmed34596798en_US
bordeaux.journalBreast Cancer Research and Treatmenten_US
bordeaux.page403-413en_US
bordeaux.volume190en_US
bordeaux.hal.laboratoriesInstitut de neurosciences cognitives et intégratives d'Aquitaine (INCIA) - UMR 5287en_US
bordeaux.issue3en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionCNRSen_US
bordeaux.teamImagerie multimodale translationnelle
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.identifierhal-04144560
hal.version1
hal.date.transferred2023-06-28T12:31:09Z
hal.exporttrue
workflow.import.sourcepubmed
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&amp;rft_val_fmt=info:ofi/fmt:kev:mtx:journal&amp;rft.jtitle=Breast%20Cancer%20Research%20and%20Treatment&amp;rft.date=2021-12-01&amp;rft.volume=190&amp;rft.issue=3&amp;rft.spage=403-413&amp;rft.epage=403-413&amp;rft.eissn=1573-7217&amp;rft.issn=1573-7217&amp;rft.au=MORGAT,%20Clement&amp;BROUSTE,%20Veronique&amp;CHASTEL,%20Adrien&amp;VELASCO,%20Valerie&amp;MACGROGAN,%20Gaetan&amp;rft.genre=article


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