@article {WESO{\L}OWSKA943, author = {OLGA WESO{\L}OWSKA and JOSEPH MOLNAR and IMRE OCSOVSZKI and KRYSTYNA MICHALAK}, title = {Differential Effect of Phenothiazines on MRP1 and P-Glycoprotein Activity}, volume = {23}, number = {6}, pages = {943--947}, year = {2009}, publisher = {International Institute of Anticancer Research}, abstract = {Background: Overexpression of ATP-binding cassette (ABC) transporters such as P-glycoprotein (P-gp), multidrug resistance-associated protein 1 (MRP1) or breast cancer resistance protein (BCRP) accounts for majority of cases of multidrug resistance (MDR) of cancer cells. Materials and Methods: In the present work, the interactions of seven commercially available phenothiazine derivatives, known P-glycoprotein inhibitors, with this transporter and MRP1 were compared. By flow cytometry, it was shown that all the drugs increased the accumulation of rhodamine 123 in the P-gp-overexpressing lymphoma cell line L5178 MDR. On the other hand, phenothiazine derivatives stimulated MRP1-mediated efflux of fluorescent probe (BCPCF) out of human erythrocytes. Results: In this way, these phenothiazine derivatives were identified as a group of atypical MDR modulators that differently interact with P-gp (as inhibitors) and MRP1 (as stimulators). Conclusion: This observation clearly shows that the activity of all new modulators should be tested for their effects towards different ABC transporters as a standard procedure.}, issn = {0258-851X}, URL = {https://iv.iiarjournals.org/content/23/6/943}, eprint = {https://iv.iiarjournals.org/content/23/6/943.full.pdf}, journal = {In Vivo} }