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Polo-like kinase inhibitor BI2536 induces eryptosis.

Authors :
Jemaà M
Mokdad Gargouri R
Lang F
Source :
Wiener medizinische Wochenschrift (1946) [Wien Med Wochenschr] 2023 Apr; Vol. 173 (5-6), pp. 152-157. Date of Electronic Publication: 2022 Sep 30.
Publication Year :
2023

Abstract

BI2536 is potent inhibitor of polo-like kinases PLK1, 2, and 3. The inhibition of PLKs in nucleated cells induces apoptosis by perturbing the cell cycle with consequent engagement of mitotic catastrophe. BI2536 is being tested as chemotherapy in various phase I/II/III clinical trials. Erythrocytes do not have a nucleus; however, they may undergo programmed suicide with characteristic hallmarks including cell shrinkage and phosphatidylserine translocation to the cell surface. This particular death is baptized eryptosis. Our study explored whether BI2536 induces eryptosis. We used flow cytometry to access death in red blood cells. We analyzed the cellular volume, the intracellular calcium concentration, the cell surface phosphatidylserine exposure, and the ceramide abundance. In addition, we analyzed the effect of BI2536 on hemolysis. Our investigation showed that after 48 h of incubation with PLK inhibitor BI2536, erythrocytes lost volume and were positive for annexin‑V without any effect on hemolysis. Cells also showed an abundance of ceramide and an increase of intracellular calcium. All these finding suggest that BI2536 provokes eryptosis in red blood cells, ostensibly in part due to Ca <superscript>2+</superscript> entry and ceramide accumulation.<br /> (© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Austria, ein Teil von Springer Nature.)

Details

Language :
English
ISSN :
1563-258X
Volume :
173
Issue :
5-6
Database :
MEDLINE
Journal :
Wiener medizinische Wochenschrift (1946)
Publication Type :
Academic Journal
Accession number :
36178637
Full Text :
https://doi.org/10.1007/s10354-022-00966-7