Identification of curaxin as a potential new therapeutic for JAK2 V617F mutant patients.
Myelofibrosis is a myeloproliferative neoplasm (MPN) which typically results in reduced length and quality of life due to systemic symptoms and blood count changes arising from fibrotic changes in the bone marrow. While the JAK2 inhibitor ruxolitinib provides some clinical benefit, there remains a s...
Main Authors: | Stella Pearson, Rognvald Blance, Fei Yan, Ya-Ching Hsieh, Bethany Geary, Fabio M R Amaral, Tim C P Somervaille, Kristina Kirschner, Anthony D Whetton, Andrew Pierce |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2023-01-01
|
Series: | PLoS ONE |
Online Access: | https://doi.org/10.1371/journal.pone.0286412 |
Similar Items
-
AXL Inhibition Extinguishes Primitive JAK2 Mutated Myeloproliferative Neoplasm Progenitor Cells
by: Stella Pearson, et al.
Published: (2019-06-01) -
Combination of curaxin and tyrosine kinase inhibitors display enhanced killing of primitive Chronic Myeloid Leukaemia cells.
by: Stella Pearson, et al.
Published: (2022-01-01) -
Mechanism of curaxin-dependent nucleosome unfolding by FACT
by: Olesya I. Volokh, et al.
Published: (2022-11-01) -
The SMAC mimetic LCL-161 selectively targets JAK2V617F mutant cells
by: Brianna M. Craver, et al.
Published: (2020-01-01) -
The telomerase inhibitor imetelstat differentially targets JAK2V617F versus CALR mutant myeloproliferative neoplasm cells and inhibits JAK-STAT signaling
by: Kathrin Olschok, et al.
Published: (2023-10-01)