This review highlights multiomics' potential utility in understanding triple-negative breast cancer biology, suggesting novel biomarkers and therapeutic targets.
Triple-negative breast cancer (TNBC) has the poorest prognosis among all breast cancer subtypes, largely due to the lack of targeted therapies and its resistance to both chemotherapy and immunotherapy. A deeper understanding of TNBC biology is therefore critical for identifying therapeutic targets. Molecular subtyping of TNBC, first introduced over a decade ago, has significantly advanced our knowledge of the disease’s biology. However, tumor heterogeneity remains a major factor contributing to poor clinical outcomes and treatment resistance. The integration of multi-omics technologies including genomic, transcriptomic, and proteomic analyses, offers a powerful approach to further dissect tumor heterogeneity and accelerate the discovery of new biomarkers and therapeutic targets. This review aims to highlight the potential utility and evolving role of multiomics (-omics) in improving our understanding of TNBC biology - particularly tumor heterogeneity - ultimately facilitating the development of novel therapies and actionable strategies to treat the disease.
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Juan et al. (2025) studied this question.
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