001     265365
005     20231120155359.0
024 7 _ |a pmid:37783677
|2 pmid
024 7 _ |a 10.1038/s41420-023-01650-4
|2 doi
024 7 _ |a pmc:PMC10545677
|2 pmc
024 7 _ |a altmetric:155311198
|2 altmetric
037 _ _ |a DZNE-2023-00989
082 _ _ |a 610
100 1 _ |a Yang, Xue
|b 0
245 _ _ |a A primary luminal/HER2 negative breast cancer patient with mismatch repair deficiency
260 _ _ |a London
|c 2023
|b Nature Publishing Group
336 7 _ |a article
|2 DRIVER
336 7 _ |a Output Types/Journal article
|2 DataCite
336 7 _ |a Journal Article
|b journal
|m journal
|0 PUB:(DE-HGF)16
|s 1697198295_22039
|2 PUB:(DE-HGF)
336 7 _ |a ARTICLE
|2 BibTeX
336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a Journal Article
|0 0
|2 EndNote
520 _ _ |a Here, we present the case of a 47-year-old woman diagnosed with luminal B breast cancer subtype and provide an in-depth analysis of her gene mutations, chromosomal alterations, mRNA and protein expression changes. We found a point mutation in the FGFR2 gene, which is potentially hyper-activating the receptor function, along with over-expression of its ligand FGF20 due to genomic amplification. The patient also harbors somatic and germline mutations in some mismatch repair (MMR) genes, with a strong MMR mutational signature. The patient displays high microsatellite instability (MSI) and tumor mutational burden (TMB) status and increased levels of CTLA-4 and PD-1 expression. Altogether, these data strongly implicate that aberrant FGFR signaling, and defective MMR system might be involved in the development of this breast tumor. In addition, high MSI and TMB in the context of CTLA-4 and PD-L1 positivity, suggest the potential benefit of immune checkpoint inhibitors. Accurate characterization of molecular subtypes, based on gene mutational and expression profiling analyses, will be certainly helpful for individualized treatment and targeted therapy of breast cancer patients, especially for those subtypes with adverse outcome.
536 _ _ |a 351 - Brain Function (POF4-351)
|0 G:(DE-HGF)POF4-351
|c POF4-351
|f POF IV
|x 0
588 _ _ |a Dataset connected to DataCite
700 1 _ |a Smirnov, Artem
|0 0000-0002-1575-8725
|b 1
700 1 _ |a Buonomo, Oreste Claudio
|b 2
700 1 _ |a Mauriello, Alessandro
|b 3
700 1 _ |a Shi, Yufang
|b 4
700 1 _ |a Bischof, Julia
|b 5
700 1 _ |a Woodsmith, Jonathan
|b 6
700 1 _ |a Bove, Pierluigi
|b 7
700 1 _ |a Rovella, Valentina
|b 8
700 1 _ |a Scimeca, Manuel
|b 9
700 1 _ |a Sica, Giuseppe
|b 10
700 1 _ |a Tisone, Giuseppe
|b 11
700 1 _ |a Wang, Ying
|b 12
700 1 _ |a Servadei, Francesca
|b 13
700 1 _ |a Melino, Gerry
|0 P:(DE-2719)9001390
|b 14
|u dzne
700 1 _ |a Candi, Eleonora
|0 0000-0001-8332-4825
|b 15
700 1 _ |a Bernassola, Francesca
|0 0000-0002-8883-8654
|b 16
773 _ _ |a 10.1038/s41420-023-01650-4
|g Vol. 9, no. 1, p. 365
|0 PERI:(DE-600)2842546-7
|n 1
|p 365
|t Cell death discovery
|v 9
|y 2023
|x 2058-7716
856 4 _ |y OpenAccess
|u https://pub.dzne.de/record/265365/files/DZNE-2023-00989.pdf
856 4 _ |y OpenAccess
|x pdfa
|u https://pub.dzne.de/record/265365/files/DZNE-2023-00989.pdf?subformat=pdfa
909 C O |o oai:pub.dzne.de:265365
|p openaire
|p open_access
|p VDB
|p driver
|p dnbdelivery
910 1 _ |a Deutsches Zentrum für Neurodegenerative Erkrankungen
|0 I:(DE-588)1065079516
|k DZNE
|b 14
|6 P:(DE-2719)9001390
913 1 _ |a DE-HGF
|b Gesundheit
|l Neurodegenerative Diseases
|1 G:(DE-HGF)POF4-350
|0 G:(DE-HGF)POF4-351
|3 G:(DE-HGF)POF4
|2 G:(DE-HGF)POF4-300
|4 G:(DE-HGF)POF
|v Brain Function
|x 0
914 1 _ |y 2023
915 _ _ |a OpenAccess
|0 StatID:(DE-HGF)0510
|2 StatID
915 _ _ |a Creative Commons Attribution CC BY 4.0
|0 LIC:(DE-HGF)CCBY4
|2 HGFVOC
915 _ _ |a JCR
|0 StatID:(DE-HGF)0100
|2 StatID
|b CELL DEATH DISCOV : 2022
|d 2023-08-22
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0200
|2 StatID
|b SCOPUS
|d 2023-08-22
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0300
|2 StatID
|b Medline
|d 2023-08-22
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0320
|2 StatID
|b PubMed Central
|d 2023-08-22
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0501
|2 StatID
|b DOAJ Seal
|d 2023-05-02T09:09:37Z
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0500
|2 StatID
|b DOAJ
|d 2023-05-02T09:09:37Z
915 _ _ |a Peer Review
|0 StatID:(DE-HGF)0030
|2 StatID
|b DOAJ : Anonymous peer review
|d 2023-05-02T09:09:37Z
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0199
|2 StatID
|b Clarivate Analytics Master Journal List
|d 2023-08-22
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1050
|2 StatID
|b BIOSIS Previews
|d 2023-08-22
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0150
|2 StatID
|b Web of Science Core Collection
|d 2023-08-22
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1030
|2 StatID
|b Current Contents - Life Sciences
|d 2023-08-22
915 _ _ |a IF >= 5
|0 StatID:(DE-HGF)9905
|2 StatID
|b CELL DEATH DISCOV : 2022
|d 2023-08-22
920 1 _ |0 I:(DE-2719)1013003
|k AG Bano
|l Aging and Neurodegeneration
|x 0
920 1 _ |0 I:(DE-2719)5000018
|k AG Nicotera
|l Synaptic Connectivity and Neurodegeneration
|x 1
980 _ _ |a journal
980 _ _ |a VDB
980 _ _ |a UNRESTRICTED
980 _ _ |a I:(DE-2719)1013003
980 _ _ |a I:(DE-2719)5000018
980 1 _ |a FullTexts


LibraryCollectionCLSMajorCLSMinorLanguageAuthor
Marc 21