Human Gene Set: CHARAFE_BREAST_CANCER_BASAL_VS_MESENCHYMAL_UP


Standard name CHARAFE_BREAST_CANCER_BASAL_VS_MESENCHYMAL_UP
Systematic name M12795
Brief description Genes up-regulated in basal-like breast cancer cell lines as compared to the mesenchymal-like ones.
Full description or abstract A better molecular characterization of breast cell lines (BCL) may help discover new markers to apply to tumour samples. We performed gene and protein expression profiling of 31 BCL using whole-genome DNA microarrays and immunohistochemistry (IHC) on 'cell microarrays' (CMA), respectively. Global hierarchical clustering discriminated two groups of BCL: group I corresponded to luminal cell lines, group II to basal and mesenchymal cell lines. Correlations with centroids calculated from a published 'intrinsic 500-gene set' assigned 15 cell lines as luminal, eight as basal and four as mesenchymal. A set of 1.233 genes was differentially expressed between basal and luminal samples. Mesenchymal and basal subtypes were rather similar and discriminated by only 227 genes. The expression of 10 proteins (CAV1, CD44, EGFR, MET, ETS1, GATA3, luminal cytokeratin CK19, basal cytokeratin CK5/6, CD10, and ERM protein moesin) encoded by luminal vs basal discriminator genes confirmed the subtype classification and the validity of the identified markers. Our BCL basal/luminal signature correctly re-classified the published series of tumour samples that originally served to identify the molecular subtypes, suggesting that the identified markers should be useful for tumour classification and might represent promising targets for disease management.
Collection C2: Curated
      CGP: Chemical and Genetic Perturbations
Source publication Pubmed 16288205   Authors: Charafe-Jauffret E,Ginestier C,Monville F,Finetti P,Adélaïde J,Cervera N,Fekairi S,Xerri L,Jacquemier J,Birnbaum D,Bertucci F
Exact source Table 4S
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Source species Homo sapiens
Contributed by Arthur Liberzon (MSigDB Team)
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identifier namespace		 AFFY_HG_U133
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Version history 3.0: First introduced

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