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Omics Technologies Improving Breast Cancer Research and Diagnostics
Open accessAbstract
Breast cancer (BC) has yielded approximately 2.26 million new cases and has caused nearly 685,000 deaths worldwide in the last two years, making it the most common diagnosed cancer type in the world. BC is an intricate ecosystem formed by both the tumor microenvironment and malignant cells, and its heterogeneity impacts the response to treatment. Biomedical research has entered the era of massive omics data thanks to the high-throughput sequencing revolution, quick progress and widespread adoption. These technologies—liquid biopsy, transcriptomics, epigenomics, proteomics, metabolomics, pharmaco-omics and artificial intelligence imaging—could help researchers and clinicians to better understand the formation and evolution of BC. This review focuses on the findings of recent multi-omics-based research that has been applied to BC research, with an introduction to every omics technique and their applications for the different BC phenotypes, biomarkers, target therapies, diagnosis, treatment and prognosis, to provide a comprehensive overview of the possibilities of BC research.
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“For instance, BRCA1 and USP44 have been reported to be of great interest in breast cancer, since the first protein is a tumor suppressor, and the second one still has an unknown oncogenic potential.”
From Revisiting Epigenetics Fundamentals and Its Biomedical Implications (2024) · cites this paper as [106]
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Integration of multi-omics data reveals a novel hybrid breast cancer subtype and its biomarkers
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Role of MRI in screening, diagnosis and management of breast cancer
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Integrated analysis of differentially expressed genes and pathways in triple-negative breast cancer
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Drug Metabolism for the Identification of Clinical Biomarkers in Breast Cancer
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Srinivasan, D., Balakrishnan, R., Chauhan, A., Kumar, J., Girija, D. M., Shrestha, R., Shrestha, R., & Subbarayan, R. (2025) · MedComm · doi:10.1002/mco2.70333 · Cited by 40
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Revisiting Epigenetics Fundamentals and Its Biomedical Implications
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Metadata
- Authors
- Orsini, A., Diquigiovanni, C., & Bonora, E.
- Affiliations
- University of Bologna (IT)
- Corresponding author
- Diquigiovanni, Chiara
- Venue
- International Journal of Molecular Sciences
- Publisher
- MDPI AG
- Published
- 2023-08-11
- Volume
- 24
- Issue
- 16
- Pages
- 12690
- ISSN
- 1422-0067 (ISSN-L)
- PMC
- PMC10454385
- OpenAlex
- W4385769695
- Cited by
- 52
- References
- 201
- Citations by year
- 2026: 10 · 2025: 26 · 2024: 15 · 2023: 1
- FWCI
- 1.64
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- International Journal of Molecular Sciences (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Archivio istituzionale della ricerca (Alma Mater Studiorum Università di Bologna) (submittedVersion, cc-by)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Breast Cancer Treatment Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer Genomics and Diagnostics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bioinformatics and Genomic Networks
- Keywords
- breast cancer, multi-omics, liquid biopsy, transcriptomics, epigenomics, proteomics, metabolomics, tumor microenvironment, tumor heterogeneity, biomarkers, targeted therapy, prognosis, diagnosis
- MeSH terms
- Artificial Intelligence, Humans, Neoplasms, Research Personnel, Ecosystem, Biomedical Research, Epigenomics
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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