Abstract
The genetic variants of the ATP-binding cassette, subfamily G, member 2 (ABCG2) are known to be involved in developing cancer risk and interindividual differences in chemotherapeutic response. The polymorphisms in ABCG2 gene were genotyped by using PCR-RFLP assays. We found that ABCG2 G34A GA/AA genotype, C421A AA genotype, and haplotypes 34A-421C and 34G-421A were significantly associated with increased risk for developing breast carcinoma. Furthermore, ABCG2 C421A AA homozygote had a significant enhanced therapeutic response in patients with neoadjuvant anthracycline-based chemotherapy. Moreover, ABCG2 G34A AA genotype carriers displayed a longer OS in ER positive patients or PR positive patients after postoperative anthracycline-based chemotherapy. These results suggested that the ABCG2 polymorphisms might be a candidate pharmacogenomic factor to assess susceptibility and prognosis for breast carcinoma patients.
Publication types
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Multicenter Study
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Randomized Controlled Trial
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Research Support, Non-U.S. Gov't
MeSH terms
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ATP Binding Cassette Transporter, Subfamily G, Member 2
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ATP-Binding Cassette Transporters / genetics*
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Adult
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Aged
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Aged, 80 and over
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Anthracyclines / administration & dosage*
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Antineoplastic Agents / administration & dosage
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Biomarkers, Tumor / genetics*
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Breast Neoplasms / drug therapy*
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Breast Neoplasms / epidemiology
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Breast Neoplasms / genetics*
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China / epidemiology
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Female
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Genetic Predisposition to Disease / epidemiology
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Genetic Predisposition to Disease / genetics
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Genetic Variation / genetics
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Humans
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Incidence
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Middle Aged
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Neoplasm Proteins / genetics*
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Polymorphism, Single Nucleotide / genetics*
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Prognosis
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Reproducibility of Results
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Risk Factors
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Sensitivity and Specificity
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Treatment Outcome
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Young Adult
Substances
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ABCG2 protein, human
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ATP Binding Cassette Transporter, Subfamily G, Member 2
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ATP-Binding Cassette Transporters
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Anthracyclines
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Antineoplastic Agents
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Biomarkers, Tumor
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Neoplasm Proteins