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Triggering of Suicidal Erythrocyte Death by Ruxolitinib
Author(s) -
Marilena Briglia,
Antonella Fazio,
Caterina Faggio,
Stefan Laufer,
Kousi Alzoubi,
Florian Läng
Publication year - 2015
Publication title -
cellular physiology and biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.486
H-Index - 87
eISSN - 1421-9778
pISSN - 1015-8987
DOI - 10.1159/000430394
Subject(s) - ruxolitinib , phosphatidylserine , kinase , annexin , p38 mitogen activated protein kinases , microbiology and biotechnology , erythropoietin , phospholipid scramblase , chemistry , annexin a5 , protein kinase a , apoptosis , pharmacology , biology , medicine , endocrinology , biochemistry , myelofibrosis , phospholipid , bone marrow , membrane
The JAK1/JAK2 tyrosine kinase inhibitor ruxolitinib is widely used for the treatment of myeloproliferative neoplasm-associated myelofibrosis and other malignancies. Most important side effects include anemia. A common cause of anemia is accelerated suicidal death of erythrocytes or eryptosis, which is characterized by cell shrinkage and cell membrane scrambling with phosphatidylserine translocation to the erythrocyte surface. Mechanisms contributing to the triggering of eryptosis include oxidative stress, Ca2+ entry with increase of cytosolic Ca2+ activity ([Ca2+]i), and activation of distinct kinases, such as p38 mitogen activated protein (MAP) kinase. The present study explored whether and how ruxolitinib induces eryptosis.

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