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Targeting the niche is a new strategy to eliminate persistent and drug-resistant LSCs.
2
This represents a novel approach to more effectively target LSCs in patients receiving TKI treatment.
3
No relapse occurred in the eight patients still on TKI therapy, whether LSCs were detectable or not.
4
These cells are thought to be responsible for relapse and are termed leukemia stem cells (LSCs).
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These findings indicate that clinically relevant eradication of LSCs can be achieved with drugs that target LSC metabolic vulnerabilities.
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Finally, it emphasizes the difficulty of detecting residual LSCs due to their rarity and their low BCR-ABL1 mRNA expression.
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We found abnormal profiles only for H3K79me2 on MLL-AF9 fusion target loci in LSCs.
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Our findings point to a promising epigenetic-based therapeutic strategy to more effectively target LSCs in patients with CML receiving TKIs.
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This simple and inexpensive approach will facilitate basic investigation of LSCs and enable screening of novel therapeutic agents targeting LSCs.
10
In a mouse model in which both pathways are activated in stem and progenitor cells, LSCs expanded under chemotherapy-induced stress.
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MAGI2-AS3 exhibited a poor expression level in LSCs than the normal human haematopoietic stem cells.
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This is primarily caused by resisting leukemic stem cells (LSCs), which prevent achievement of treatment-free remission in all patients.
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Here we studied the ability of MSCs to support the growth and survival of leukemic stem cells (LSCs) in vitro.
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Aim: To explore the effects and mechanism of the spleen on the proliferation and differentiation of LSCs in PH due to liver cirrhosis.
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Leukaemia stem cells (LSCs) initiate and maintain the clonal hierarchy of AML and exhibit properties of self-renewal remaining recalcitrant to conventional chemotherapy.
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Radioactivity recovery in HPLC-MSC analysis was reliably determined using an LSC-based method.