Decoding Breast Cancer: Emerging Molecular Biomarkers and Novel Therapeutic Targets for Precision Medicine

Breast cancer is the most frequent gynecological malignancy and the main cause of cancer death in the female population worldwide. One of the most significant challenges in its clinical management is the molecular heterogeneity of malignant breast tumors, which is reflected in the current molecular classification of these entities. In each of these tumor molecular subtypes, distinct genetic alterations are involved, and several intracellular signaling pathways contribute to defining their biological identity and clinical response. This literature review summarized the main classic and emerging biomarkers in breast cancer, along with the therapies associated with them. There are several classic biomarkers associated with this disease, such as estrogen and progesterone receptors, the HER2 receptor, and the Ki-67 cell proliferation marker. Given the limitations of these biomarkers, new biomarkers have been identified, including the <i>TP53</i> tumor suppressor gene, the EGFR, different types of RNAs, plus epigenetic and immunological biomarkers. The integration of classic and emerging biomarkers along with new therapeutic targets in the clinical practice has promoted a thorough understanding of the high molecular complexity of breast cancer and the development of precision medicine strategies which increase the chances of therapeutic success.

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Publication Details

Journal
International Journal of Molecular Sciences
Published
2025-12-22
DOI
https://doi.org/10.3390/ijms27010138
Primary Topic
HER2/EGFR in Cancer Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Decoding Breast Cancer: Emerging Molecular Biomarkers and Novel Therapeutic Targets for Precision Medicine

Juan Carlos Pozo Palacios, Gabriele Davide Bigoni Ordóñez, Vanessa Romero, Dámaris P. Intriago-Baldeón et al.
International Journal of Molecular Sciences
HER2/EGFR in Cancer Research
article

Decoding Breast Cancer: Emerging Molecular Biomarkers and Novel Therapeutic Targets for Precision Medicine

Juan Carlos Pozo Palacios, Gabriele Davide Bigoni Ordóñez, Vanessa Romero, Dámaris P. Intriago-Baldeón, Eduarda Sofía Pérez-Coral, Martina Isabella Armas Samaniego
article en

Abstract

Breast cancer is the most frequent gynecological malignancy and the main cause of cancer death in the female population worldwide. One of the most significant challenges in its clinical management is the molecular heterogeneity of malignant breast tumors, which is reflected in the current molecular classification of these entities. In each of these tumor molecular subtypes, distinct genetic alterations are involved, and several intracellular signaling pathways contribute to defining their biological identity and clinical response. This literature review summarized the main classic and emerging biomarkers in breast cancer, along with the therapies associated with them. There are several classic biomarkers associated with this disease, such as estrogen and progesterone receptors, the HER2 receptor, and the Ki-67 cell proliferation marker. Given the limitations of these biomarkers, new biomarkers have been identified, including the <i>TP53</i> tumor suppressor gene, the EGFR, different types of RNAs, plus epigenetic and immunological biomarkers. The integration of classic and emerging biomarkers along with new therapeutic targets in the clinical practice has promoted a thorough understanding of the high molecular complexity of breast cancer and the development of precision medicine strategies which increase the chances of therapeutic success.

International Journal of Molecular SciencesVol. 27(1)
University of Cuenca (EC), Universidad Internacional SEK (EC), Universidad San Francisco de Quito (EC)
Universidad de Cuenca
Good health and well-being
Openalex Percentile: Top 32%
HER2/EGFR in Cancer Research
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Decoding Breast Cancer: Emerging Molecular Biomarkers and Novel Therapeutic Targets for Precision Medicine — Juan Carlos Pozo Palacios, Gabriele Davide Bigoni Ordóñez, et al. · International Journal of Molecular Sciences (2025) | TGRS Research Map | TGRS