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HORMAD1 overexpression predicts response to anthracycline-cyclophosphamide and survival in triple-negative breast cancers.
- Source :
-
Molecular oncology [Mol Oncol] 2023 Oct; Vol. 17 (10), pp. 2017-2028. Date of Electronic Publication: 2023 Mar 23. - Publication Year :
- 2023
-
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.<br /> (© 2023 The Authors. Molecular Oncology published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies.)
- Subjects :
- Humans
Anthracyclines pharmacology
Anthracyclines therapeutic use
Disease-Free Survival
Antibiotics, Antineoplastic therapeutic use
Cyclophosphamide pharmacology
Cyclophosphamide therapeutic use
Cell Cycle Proteins
Triple Negative Breast Neoplasms drug therapy
Triple Negative Breast Neoplasms genetics
Triple Negative Breast Neoplasms pathology
Subjects
Details
- Language :
- English
- ISSN :
- 1878-0261
- Volume :
- 17
- Issue :
- 10
- Database :
- MEDLINE
- Journal :
- Molecular oncology
- Publication Type :
- Academic Journal
- Accession number :
- 36852691
- Full Text :
- https://doi.org/10.1002/1878-0261.13412