ABCG2, also known as the breast cancer resistance protein (BCRP), is an ATP-binding cassette transporter involved in multidrug resistance (MDR) in cancer and pharmacological barrier functions . It regulates the efflux of xenobiotics, chemotherapeutic agents, and endogenous substrates (e.g., uric acid) .
Antibodies targeting ABCG2 are pivotal for:
Flow cytometry: Quantifying ABCG2 expression in erythrocytes and cancer cells .
Immunohistochemistry (IHC): Detecting ABCG2 in tissue samples (e.g., placenta, cancer biopsies) .
Drug resistance studies: Identifying ABCG2 overexpression in chemotherapy-resistant cancers .
Genetic Variants: The Q141K polymorphism reduces ABCG2 expression by ~50% in erythrocytes, impacting uric acid metabolism and drug pharmacokinetics .
Cancer Resistance:
Blood Group System: ABCG2 encodes the Junior (Jr) blood group antigen; Jr(a−) individuals lack functional ABCG2 .
Substrate Specificity: Mutations at residue 482 (e.g., R482G/T) alter substrate affinity, enhancing efflux of anthracyclines (e.g., doxorubicin) .
Modulation: ABCG2 inhibitors (e.g., novobiocin, KO-143) reverse drug resistance in vitro .
Biomarker Potential: Erythrocyte ABCG2 levels may predict tissue-specific expression patterns and drug response .
Therapeutic Targeting: Antibodies like BXP-34 enable personalized diagnostics for optimizing chemotherapy regimens .