Articles with "mll af4" as a keyword



MiR‐27a downregulates 14‐3‐3θ, RUNX1, AF4, and MLL‐AF4, crucial drivers of blast transformation in t(4;11) leukemia cells

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Published in 2022 at "Cell Biochemistry and Function"

DOI: 10.1002/cbf.3736

Abstract: The chromosomal translocation t(4;11)(q21;q23), a hallmark of an aggressive form of acute lymphoblastic leukemia (ALL), encodes mixed‐lineage leukemia (MLL)‐AF4 oncogenic chimera that triggers aberrant transcription of genes involved in lymphocyte differentiation, including HOXA9 and MEIS1.… read more here.

Keywords: af4 mll; mir 27a; mll af4; leukemia ... See more keywords

MLL-AF4 Spreading Identifies Binding Sites that Are Distinct from Super-Enhancers and that Govern Sensitivity to DOT1L Inhibition in Leukemia

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Published in 2017 at "Cell Reports"

DOI: 10.1016/j.celrep.2016.12.054

Abstract: Summary Understanding the underlying molecular mechanisms of defined cancers is crucial for effective personalized therapies. Translocations of the mixed-lineage leukemia (MLL) gene produce fusion proteins such as MLL-AF4 that disrupt epigenetic pathways and cause poor-prognosis… read more here.

Keywords: mll af4; af4 spreading; sensitivity; gene ... See more keywords

Antileukemic Efficacy of BET Inhibitor in a Preclinical Mouse Model of MLL-AF4+ Infant ALL

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Published in 2018 at "Molecular Cancer Therapeutics"

DOI: 10.1158/1535-7163.mct-17-1123

Abstract: MLL-rearranged acute lymphoblastic leukemia (ALL) occurring in infants is a rare but very aggressive leukemia, typically associated with a dismal prognosis. Despite the development of specific therapeutic protocols, infant patients with MLL-rearranged ALL still suffer… read more here.

Keywords: mll af4; model mll; mouse model; mll rearranged ... See more keywords

Abstract 4937: Immunoproteasome inhibitors for the treatment of t(4;11)-driven ALL

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Published in 2023 at "Cancer Research"

DOI: 10.1158/1538-7445.am2023-4937

Abstract: The t(4;11)(q21;q23) chromosomal translocation that creates the MLL-AF4 fusion protein, confers a poor prognosis in infant acute lymphoblastic leukemia (ALL). This translocation also sensitizes cells to proteasome inhibitors bortezomib and carfilzomib, which are approved by… read more here.

Keywords: abstract 4937; mll af4; treatment driven; inhibitors treatment ... See more keywords

The full transforming capacity of MLL-Af4 is interlinked with lymphoid lineage commitment.

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Published in 2017 at "Blood"

DOI: 10.1182/blood-2017-04-777185

Abstract: Chromosome rearrangements involving the mixed-lineage leukemia gene (MLL) create MLL-fusion proteins, which could drive both acute lymphoblastic leukemia (ALL) and acute myeloid leukemia (AML). The lineage decision of MLL-fusion leukemia is influenced by the fusion… read more here.

Keywords: mll af4; af4 interlinked; lineage; fusion ... See more keywords

Novel Small Molecule Inhibitor Against IGF2BP3 with Potent Anti-Leukemic Activity

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Published in 2024 at "Blood"

DOI: 10.1182/blood-2024-204473

Abstract: Background:RNA binding proteins have emerged as promising therapeutic targets in cancer because of their role as important mediators of oncogenesis. The RNA binding protein IGF2BP3 is an oncofetal protein expressed during fetal development, absent or… read more here.

Keywords: mll; mll af4; i3in 002; igf2bp3 ... See more keywords

NG2 is a target gene of MLL-AF4 and underlies glucocorticoid resistance in MLL-r B-ALL by regulating NR3C1 expression.

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Published in 2024 at "Blood"

DOI: 10.1182/blood.2023022050

Abstract: B-cell acute lymphoblastic leukemia (B-ALL) is the most common pediatric cancer, with long-term overall survival rates of ~85%. However, B-ALL harboring rearrangements of the MLL gene (also known as KMT2A), referred to as MLLr B-ALL,… read more here.

Keywords: resistance; mll af4; target gene; expression ... See more keywords

Enhanced hemato-endothelial specification during human embryonic differentiation through developmental cooperation between AF4-MLL and MLL-AF4 fusions

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Published in 2019 at "Haematologica"

DOI: 10.3324/haematol.2018.202044

Abstract: The t(4;11)(q21;q23) translocation is associated with high-risk infant pro-B-cell acute lymphoblastic leukemia and arises prenatally during embryonic/fetal hematopoiesis. The developmental/pathogenic contribution of the t(4;11)-resulting MLL-AF4 (MA4) and AF4-MLL (A4M) fusions remains unclear; MA4 is always… read more here.

Keywords: mll af4; differentiation; fusion; hemato endothelial ... See more keywords