Natural Inhibitors of P-glycoprotein in Acute Myeloid Leukemia

Int J Mol Sci. 2023 Feb 18;24(4):4140. doi: 10.3390/ijms24044140.

Abstract

Acute myeloid leukemia (AML) remains an insidious neoplasm due to the percentage of patients who develop resistance to both classic chemotherapy and emerging drugs. Multidrug resistance (MDR) is a complex process determined by multiple mechanisms, and it is often caused by the overexpression of efflux pumps, the most important of which is P-glycoprotein (P-gp). This mini-review aims to examine the advantages of using natural substances as P-gp inhibitors, focusing on four molecules: phytol, curcumin, lupeol, and heptacosane, and their mechanism of action in AML.

Keywords: P-glycoprotein; acute myeloid leukemia; multidrug resistance; natural substances.

Publication types

  • Review

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B, Member 1* / antagonists & inhibitors
  • Curcumin* / therapeutic use
  • Drug Resistance, Multiple
  • Drug Resistance, Neoplasm
  • Humans
  • Leukemia, Myeloid, Acute* / drug therapy

Substances

  • ATP Binding Cassette Transporter, Subfamily B, Member 1
  • Curcumin

Grants and funding

This research received no external funding.