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- W3135480237 endingPage "103281" @default.
- W3135480237 startingPage "103281" @default.
- W3135480237 abstract "Acute myeloid leukemia (AML) is one of the most common hematological neoplasia causing death worldwide. The long-term overall survival is unsatisfactory due to many factors including older age, genetic heterogeneity and molecular characteristics comprising additional mutations, and resistance to chemotherapeutic drugs. The expression of ABCB1/P-glycoprotein, ABCC1/MRP1, ABCG2/BCRP and LRP transporter proteins is considered the major reason for multidrug resistance (MDR) in AML, however conflicting data have been reported. Here, we review the main issues about drug transporter proteins in AML clinical scenario, and highlight the clinicopathological significance of MDR phenotype associated with ABCB1 polymorphisms and FLT3 mutation." @default.
- W3135480237 created "2021-03-15" @default.
- W3135480237 creator A5010660227 @default.
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- W3135480237 creator A5046981054 @default.
- W3135480237 creator A5067156449 @default.
- W3135480237 creator A5086610740 @default.
- W3135480237 date "2021-04-01" @default.
- W3135480237 modified "2023-10-03" @default.
- W3135480237 title "Update on drug transporter proteins in acute myeloid leukemia: Pathological implication and clinical setting" @default.
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