» Articles » PMID: 38141369

Progress in Characterizing ABC Multidrug Transporters in Zebrafish

Overview
Date 2023 Dec 23
PMID 38141369
Authors
Affiliations
Soon will be listed here.
Abstract

Zebrafish have proved to be invaluable for modeling complex physiological processes shared by all vertebrate animals. Resistance of cancers and other diseases to drug treatment can occur owing to expression of the ATP-dependent multidrug transporters ABCB1, ABCG2, and ABCC1, either because of expression of these transporters by the target cells to reduce intracellular concentrations of cytotoxic drugs at barrier sites such as the blood-brain barrier (BBB) to limit penetration of drugs into privileged compartments, or by affecting the absorption, distribution, and excretion of drugs administered orally, through the skin, or directly into the bloodstream. We describe the drug specificity, cellular localization, and function of zebrafish orthologs of multidrug resistance ABC transporters with the goal of developing zebrafish models to explore the physiological and pathophysiological functions of these transporters. Finally, we provide context demonstrating the utility of zebrafish in studying cancer drug resistance. Our ultimate goal is to improve treatment of cancer and other diseases which are affected by ABC multidrug resistance transporters.

Citing Articles

Conversion of Human Multidrug Transporter P-glycoprotein (ABCB1) from Drug Efflux to Uptake Pump: Evidence for a Switch Region Modulating the Direction of Substrate Transport.

Sajid A, Ranganathan N, Guha R, Murakami M, Ahmed S, Durell S J Mol Biol. 2025; 437(7):168979.

PMID: 39900286 PMC: 11875896. DOI: 10.1016/j.jmb.2025.168979.


Abcg2a is the functional homolog of human ABCG2 expressed at the zebrafish blood-brain barrier.

Thomas J, Frye W, Robey R, Warner A, Butcher D, Matta J Fluids Barriers CNS. 2024; 21(1):27.

PMID: 38491505 PMC: 10941402. DOI: 10.1186/s12987-024-00529-5.

References
1.
Jeong J, Kwon H, Ahn J, Kang D, Kwon S, Park J . Functional and developmental analysis of the blood-brain barrier in zebrafish. Brain Res Bull. 2008; 75(5):619-28. DOI: 10.1016/j.brainresbull.2007.10.043. View

2.
Wijnholds J, Evers R, van Leusden M, Mol C, Zaman G, Mayer U . Increased sensitivity to anticancer drugs and decreased inflammatory response in mice lacking the multidrug resistance-associated protein. Nat Med. 1997; 3(11):1275-9. DOI: 10.1038/nm1197-1275. View

3.
Lorico A, Rappa G, Finch R, Yang D, Flavell R, Sartorelli A . Disruption of the murine MRP (multidrug resistance protein) gene leads to increased sensitivity to etoposide (VP-16) and increased levels of glutathione. Cancer Res. 1997; 57(23):5238-42. View

4.
Paul C, Devine A, Bishop K, Xu Q, Wulftange W, Burr H . Human macrophages survive and adopt activated genotypes in living zebrafish. Sci Rep. 2019; 9(1):1759. PMC: 6370805. DOI: 10.1038/s41598-018-38186-y. View

5.
Luckenbach T, Fischer S, Sturm A . Current advances on ABC drug transporters in fish. Comp Biochem Physiol C Toxicol Pharmacol. 2014; 165:28-52. DOI: 10.1016/j.cbpc.2014.05.002. View