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Transcriptomic immunologic signature associated with favorable clinical outcome in basal-like breast tumors

AutorMartínez-Canales, Sandra; Cifuentes, Francisco; López De Rodas Gregorio, Miguel; Serrano-Oviedo, Leticia; Galán-Moya, Eva María; Amir, Eitan; Pandiella, Atanasio ; Győrffy, Balázs; Ocaña, Alberto
Fecha de publicación2017
EditorPublic Library of Science
CitaciónPLoS ONE 12(5): e0175128 (2017)
Resumen[Background]: Most patients with early stage triple negative breast cancer (TNBC) receive adjuvant chemotherapy. Activation of the immune system is associated with tumor response and may help identify TNBC with favorable outcome. [Methods]: Gene expression data were obtained from the GEO Dataset GDS2250/GSE3744. Affymetrix CEL files were downloaded and analyzed with Affymetrix Transcriptome Analysis Console 3.0. Functional genomics was implemented with David Bioinformatics Resources 6.8. Data contained at Oncomine were used to identify genes upregulated in basal-like cancer compared to normal breast tissue. Data contained at cBioportal were used to assess for molecular alterations. The KMPlotter online tool, METABRIC and GSE25066 datasets were used to associate gene signatures with clinical outcome. [Results]: 1564 upregulated genes were identified as differentially expressed between normal and basal-like tumors. Of these, 16 genes associated with immune function were linked with clinical outcome. HLA-C, HLA-F, HLA-G and TIGIT were associated with both improved relapse-free survival (RFS) and overall survival (OS). The combination of HLA-F/TIGIT and HLA-C/HLA-F/TIGIT showed the most favorable outcome (HR for RFS 0.44, p<0.001; HR for OS 0.22, p<0.001; and HR for RFS 0.46, p<0.001; HR for OS 0.15, p<0.001; respectively). The association of HLA-C/HLA-F with outcome was confirmed using the METABRIC and GSE25066 datasets. No copy number alterations of these genes were identified. [Conclusion]: We describe a gene signature associated with immune function and favorable outcome in basal-like breast cancer. Incorporation of this signature in prospective studies may help to stratify risk of early stage TNBC.
Versión del editorhttps://doi.org/10.1371/journal.pone.0175128
URIhttp://hdl.handle.net/10261/168798
Identificadoresdoi: 10.1371/journal.pone.0175128
e-issn: 1932-6203
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