H3K4 acetylation, H3K9 acetylation and H3K27 methylation in breast tumor molecular subtypes

Author:

Judes Gaëlle12,Dagdemir Aslihan12,Karsli-Ceppioglu Seher123,Lebert André4,Echegut Maureen3,Ngollo Marjolaine23,Bignon Yves-Jean23,Penault-Llorca Frédérique25,Bernard-Gallon Dominique12

Affiliation:

1. Department of Oncogenetics, Centre Jean Perrin, CBRV, 28 Place Henri Dunant, 63001 Clermont-Ferrand, France

2. EA 4677 ‘ERTICA’, University of Auvergne, 63011 Clermont-Ferrand, France

3. Department of Toxicology, Faculty of Pharmacy, Marmara University, 34668 Istanbul, Turkey

4. University Blaise Pascal, Pascal Institute UMR 6602 CNRS/UBP, 63177 Aubière, France

5. Department of Biopathology, Centre Jean Perrin, 63011 Clermont-Ferrand, France

Abstract

Aim: Here, we investigated how the St Gallen breast molecular subtypes displayed distinct histone H3 profiles. Patients & methods: 192 breast tumors divided into five St Gallen molecular subtypes (luminal A, luminal B HER2-, luminal B HER2+, HER2+ and basal-like) were evaluated for their histone H3 modifications on gene promoters. Results: ANOVA analysis allowed to identify specific H3 signatures according to three groups of genes: hormonal receptor genes (ERS1, ERS2, PGR), genes modifying histones (EZH2, P300, SRC3) and tumor suppressor gene (BRCA1). A similar profile inside high-risk cancers (luminal B [HER2+], HER2+ and basal-like) compared with low-risk cancers including luminal A and luminal B (HER2-) were demonstrated. Conclusion: The H3 modifications might contribute to clarify the differences between breast cancer subtypes.

Publisher

Future Medicine Ltd

Subject

Cancer Research,Genetics

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