ArticleBreast cancer research and treatment2012
Oncogene amplification in male breast cancer: analysis by multiplex ligation-dependent probe amplification.
Article in Breast cancer research and treatment, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.
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28 citing papers in PubMed, 56 citations in OpenAlex.
- Analysis of the Clinical Advancements forCancers · 2022Review
- Molecular profiling of male breast cancer by multigene panel testing: Implications for precision oncology.Frontiers in oncology · 2022Article
- The Research Progress in Physiological and Pathological Functions of TRAF4.Frontiers in oncology · 2022Review
- Genetic Landscape of Male Breast Cancer.Cancers · 2021Review
- Identification of Nucleolin as a Novel AEG-1-Interacting Protein in Breast Cancer via Interactome Profiling.Cancers · 2021Article
- Elastosis in ERα-positive male breast cancer.Virchows Archiv : an international journal of pathology · 2021Article
- Methylation Profile of X-Chromosome-Related Genes in Male Breast Cancer.Frontiers in oncology · 2020Article
- The molecular genetic make-up of male breast cancer.Endocrine-related cancer · 2019Article
- TRAF4 binds to the juxtamembrane region of EGFR directly and promotes kinase activation.Proceedings of the National Academy of Sciences of the United States of America · 2018Article
- Analysis of the ATR-Chk1 and ATM-Chk2 pathways in male breast cancer revealed the prognostic significance of ATR expression.Scientific reports · 2017Article
- Germline EMSY sequence alterations in hereditary breast cancer and ovarian cancer families.BMC cancer · 2017Article
- Somatic alterations of targetable oncogenes are frequently observed in BRCA1/2 mutation negative male breast cancers.Oncotarget · 2016Article
- Prognostic models in male breast cancer.Breast cancer research and treatment · 2016Article
- HMG-CoAR expression in male breast cancer: relationship with hormone receptors, Hippo transducers and survival outcomes.Scientific reports · 2016Article
- BIRC5 Genomic Copy Number Variation in Early-Onset Breast Cancer.Iranian biomedical journal · 2016Article
- Expression of phosphorylated eIF4E-binding protein 1, but not of eIF4E itself, predicts survival in male breast cancer.British journal of cancer · 2016Article
- Article
- Clinical relevance of copy number profiling in oral and oropharyngeal squamous cell carcinoma.Cancer medicine · 2015Article
- Chromosome 17 copy number changes in male breast cancer.Cellular oncology (Dordrecht, Netherlands) · 2015Article
- Immunohistochemical, genetic and epigenetic profiles of hereditary and triple negative breast cancers. Relevance in personalized medicine.American journal of cancer research · 2015Article
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Authors and funding
8 authors at 6 institutions in 3 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Gene amplification is an important mechanism for oncogene activation, a crucial step in carcinogenesis. Compared to female breast cancer, little is known on the genetic makeup of male breast cancer, because large series are lacking. Copy number changes of 21 breast cancer related genes were studied in 110 male breast cancers using multiplex ligation-dependent probe amplification. A ratio of >1.3 was regarded indicative for gene copy number gain and a ratio >2.0 for gene amplification. Data were correlated with clinicopathological features, prognosis and 17 genes were compared with a group of female breast cancers. Gene copy number gain of CCND1, TRAF4, CDC6 and MTDH was seen in >40 % of the male breast cancer cases, with also frequent amplification. The number of genes with copy number gain and several single genes were associated with high grade, but only CCND1 amplification was an independent predictor of adverse survival in Cox regression (p = 0.015; hazard ratio 3.0). In unsupervised hierarchical clustering a distinctive group of male breast cancer with poor prognosis (p = 0.009; hazard ratio 3.4) was identified, characterized by frequent CCND1, MTDH, CDC6, ADAM9, TRAF4 and MYC copy number gain. Compared to female breast cancers, EGFR (p = 0.005) and CCND1 (p = 0.041) copy number gain was more often seen in male breast cancer, while copy number gain of EMSY (p = 0.004) and CPD (p = 0.001) and amplification in general was less frequent. In conclusion, several female breast cancer genes also seem to be important in male breast carcinogenesis. However, there are also clear differences in copy number changes between male and female breast cancers, pointing toward differences in carcinogenesis between male and female breast cancer and emphasizing the importance of identifying biomarkers and therapeutic agents based on research in male breast cancer. In addition CCND1 amplification seems to be an independent prognosticator in male breast cancer.
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