Abstract
Anthracyclines are frequently used in the adjuvant setting for breast cancer treatment since it is considered that anthracycline-based chemotherapy treatment benefits breast cancer patients. Nonetheless, these drugs are associated with severe side effects and predictive factors, for sensitivity to anthracyclines, are warranted in clinical practice. Topoisomerase 2 alpha (TOP2A) is considered to be the molecular target of these drugs. The potential predictive value of TOP2A amplification and overexpression has been extensively studied in breast cancer patients treated with anthracyclines. However, results are not conclusive. In this paper, we review some of the published studies addressing the predictive value of TOP2A as well as the cellular functions of this enzyme and its status in breast cancer tissue.
Publication types
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Evaluation Study
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Research Support, Non-U.S. Gov't
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Review
MeSH terms
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Animals
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Anthracyclines / therapeutic use*
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Antigens, Neoplasm / genetics
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Antigens, Neoplasm / metabolism
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Antigens, Neoplasm / physiology*
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Antineoplastic Agents / therapeutic use
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Biomarkers, Pharmacological / analysis
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Biomarkers, Pharmacological / metabolism
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Biomarkers, Tumor / genetics
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Biomarkers, Tumor / metabolism
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Biomarkers, Tumor / physiology
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Breast Neoplasms / diagnosis
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Breast Neoplasms / drug therapy
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Carcinoma / diagnosis
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Carcinoma / drug therapy
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DNA Topoisomerases, Type II / genetics
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DNA Topoisomerases, Type II / metabolism
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DNA Topoisomerases, Type II / physiology*
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DNA-Binding Proteins / genetics
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DNA-Binding Proteins / metabolism
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DNA-Binding Proteins / physiology*
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Female
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Humans
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Models, Biological
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Poly-ADP-Ribose Binding Proteins
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Predictive Value of Tests
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Prognosis
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Treatment Outcome
Substances
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Anthracyclines
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Antigens, Neoplasm
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Antineoplastic Agents
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Biomarkers, Pharmacological
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Biomarkers, Tumor
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DNA-Binding Proteins
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Poly-ADP-Ribose Binding Proteins
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DNA Topoisomerases, Type II
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TOP2A protein, human