ATP-Binding Cassette Subfamily G Member 2 in Acute Myeloid Leukemia: A New Molecular Target?
Daniela DamianiMario TiribelliPublished in: Biomedicines (2024)
Despite the progress in the knowledge of disease pathogenesis and the identification of many molecular markers as potential targets of new therapies, the cure of acute myeloid leukemia remains challenging. Disease recurrence after an initial response and the development of resistance to old and new therapies account for the poor survival rate and still make allogeneic stem cell transplantation the only curative option. Multidrug resistance (MDR) is a multifactorial phenomenon resulting from host-related characteristics and leukemia factors. Among these, the overexpression of membrane drug transporter proteins belonging to the ABC (ATP-Binding Cassette)-protein superfamily, which diverts drugs from their cellular targets, plays an important role. Moreover, a better understanding of leukemia biology has highlighted that, at least in cancer, ABC protein's role goes beyond simple drug transport and affects many other cell functions. In this paper, we summarized the current knowledge of ABCG2 (formerly Breast Cancer Resistance Protein, BCRP) in acute myeloid leukemia and discuss the potential ways to overcome its efflux function and to revert its ability to confer stemness to leukemia cells, favoring the persistence of leukemia progenitors in the bone marrow niche and justifying relapse also after therapy intensification with allogeneic stem cell transplantation.
Keyphrases
- stem cell transplantation
- acute myeloid leukemia
- bone marrow
- high dose
- healthcare
- binding protein
- allogeneic hematopoietic stem cell transplantation
- mesenchymal stem cells
- protein protein
- induced apoptosis
- stem cells
- amino acid
- multidrug resistant
- emergency department
- cell proliferation
- epithelial mesenchymal transition
- drug induced
- transcription factor
- cell therapy
- human health
- dna binding
- single molecule
- free survival
- climate change
- cancer stem cells
- replacement therapy