HORMAD1 overexpression predicts response to anthracycline–cyclophosphamide and survival in triple‐negative breast cancers

Author:

El‐Botty Rania1,Vacher Sophie2,Mainguené Juliette23ORCID,Briaux Adrien2,Ibadioune Sabrina2,Dahmani Ahmed1,Montaudon Elodie1,Nemati Fariba1,Huguet Léa1,Sourd Laura1,Morriset Ludivine1,Château‐Joubert Sophie4,Dubois Thierry1,Maire Virginie1,Lidereau Rosette2,Rapinat Audrey1,Gentien David1,Coussy Florence23,Bièche Ivan25,Marangoni Elisabetta1ORCID

Affiliation:

1. Translational Research Department, Institut Curie PSL Research University Paris France

2. Department of Genetics, Institut Curie PSL Research University Paris France

3. Medical Oncology Department, Institut Curie PSL Research University Paris France

4. BioPole Alfort, Ecole Nationale Vétérinaire d'Alfort Maisons Alfort France

5. Faculty of Pharmaceutical and Biological Sciences Paris City University, Inserm U1016 France

Abstract

Triple negative breast cancers (TNBCs) represent 15–20% of all breast cancers and are associated with higher recurrence and distant metastasis rate. Standard of care for early stage TNBC is anthracyclines combined with cyclophosphamide (AC) followed by taxanes, in the neo‐adjuvant or adjuvant setting. This work aimed to identify predictive biomarkers of AC response in patient‐derived xenograft (PDX) models of TNBC and to validate them in the clinical setting. By gene and protein expression analysis of 39 PDX with different responses to AC, we found that high expression of HORMAD1 was associated with better response to AC. Both gene and protein expression were associated with promoter hypomethylation. In a cohort of 526 breast cancer patients, HORMAD1 was overexpressed in 71% of TNBC. In a second cohort of 186 TNBC patients treated with AC, HORMAD1 expression was associated with longer metastasis‐free survival (MFS). In summary, HORMAD1 overexpression was predictive of an improved response to AC in PDX and is an independent prognostic factor in TNBC patients treated with AC.

Publisher

Wiley

Subject

Cancer Research,Genetics,Molecular Medicine,General Medicine,Oncology

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