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Pro-Coagulant and Pro-Thrombotic Effects of Paclitaxel Mediated by Red Blood Cells

Authors
Kim, KeunyoungChang, Youn-KyeongBian, YiyingBae, Ok-NamLim, Kyung-MinChung, Jin-Ho
Issue Date
Oct-2018
Publisher
GEORG THIEME VERLAG KG
Keywords
paclitaxel; anti-cancer drug; thrombosis; red blood cells; phosphatidylserine exposure; microvesicle release
Citation
THROMBOSIS AND HAEMOSTASIS, v.118, no.10, pp 1765 - 1775
Pages
11
Indexed
SCI
SCIE
SCOPUS
Journal Title
THROMBOSIS AND HAEMOSTASIS
Volume
118
Number
10
Start Page
1765
End Page
1775
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/5292
DOI
10.1055/s-0038-1670659
ISSN
0340-6245
2567-689X
Abstract
Background Paclitaxel is one of the most widely used anti-cancer drugs, but numerous case reports of thrombotic events in the cancer patients using paclitaxel raise concern over its pro-thrombotic risk. Materials and Methods We investigated whether paclitaxel can elicit pro-thrombotic properties in red blood cells (RBCs) through phosphatidylserine (PS) exposure and microvesicle (MV) release. Results In freshly isolated human RBCs, paclitaxel induced thrombin generation through PS exposure and MV release, whereas either coagulation factors or platelets were unaffected. Paclitaxel-induced PS exposure in RBC was mediated by scramblase activation which was induced by calcium-independent protein kinase C (PKC). activation. Paclitaxel also increased RBC-endothelial cell adhesion and RBC aggregate formation which can also contribute to thrombosis. Indeed, intravenous administration of paclitaxel to rats induced PS exposure and PKC. activation in RBCs in vivo which ultimately promoted venous thrombus formation. Conclusion These results demonstrated that paclitaxel may elicit pro-thrombotic properties in RBCs through PS exposure andMV release, which can ultimately promote thrombus formation.
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