[HTML][HTML] Multifaceted role of PRDM proteins in human cancer
The PR/SET domain family (PRDM) comprise a family of genes whose protein products
share a conserved N-terminal PR [PRDI-BF1 (positive regulatory domain I-binding factor 1) …
share a conserved N-terminal PR [PRDI-BF1 (positive regulatory domain I-binding factor 1) …
[HTML][HTML] EVI1 dysregulation: impact on biology and therapy of myeloid malignancies
C Birdwell, W Fiskus, TM Kadia, CD DiNardo… - Blood cancer …, 2021 - nature.com
Ecotropic viral integration site 1 (Evi1) was discovered in 1988 as a common site of
ecotropic viral integration resulting in myeloid malignancies in mice. EVI1 is an oncogenic …
ecotropic viral integration resulting in myeloid malignancies in mice. EVI1 is an oncogenic …
[HTML][HTML] Epigenetic landscape reveals MECOM as an endothelial lineage regulator
A comprehensive understanding of endothelial cell lineage specification will advance
cardiovascular regenerative medicine. Recent studies found that unique epigenetic …
cardiovascular regenerative medicine. Recent studies found that unique epigenetic …
[PDF][PDF] Multipotent progenitors and hematopoietic stem cells arise independently from hemogenic endothelium in the mouse embryo
T Dignum, B Varnum-Finney, SR Srivatsan, S Dozono… - Cell reports, 2021 - cell.com
During embryogenesis, waves of hematopoietic progenitors develop from hemogenic
endothelium (HE) prior to the emergence of self-renewing hematopoietic stem cells (HSCs) …
endothelium (HE) prior to the emergence of self-renewing hematopoietic stem cells (HSCs) …
MECOM-associated syndrome: a heterogeneous inherited bone marrow failure syndrome with amegakaryocytic thrombocytopenia
M Germeshausen, P Ancliff, J Estrada… - Blood …, 2018 - ashpublications.org
Heterozygous mutations in MECOM (MDS1 and EVI1 complex locus) have been reported to
be causative of a rare association of congenital amegakaryocytic thrombocytopenia and …
be causative of a rare association of congenital amegakaryocytic thrombocytopenia and …
The creatine kinase pathway is a metabolic vulnerability in EVI1-positive acute myeloid leukemia
N Fenouille, CF Bassil, I Ben-Sahra, L Benajiba… - Nature medicine, 2017 - nature.com
Expression of the MECOM (also known as EVI1) proto-oncogene is deregulated by
chromosomal translocations in some cases of acute myeloid leukemia (AML) and is …
chromosomal translocations in some cases of acute myeloid leukemia (AML) and is …
The role of PRDMs in cancer: one family, two sides
The PRDM family of proteins share a unique structure, with an N-terminal PR domain, which
has a potential methyltransferase activity, followed by a distinct number of zinc fingers at the …
has a potential methyltransferase activity, followed by a distinct number of zinc fingers at the …
EVI1 drives leukemogenesis through aberrant ERG activation
J Schmoellerl, IAM Barbosa, M Minnich, F Andersch… - Blood, 2023 - ashpublications.org
Chromosomal rearrangements involving the MDS1 and EVI1 complex locus (MECOM) on
chromosome 3q26 define an aggressive subtype of acute myeloid leukemia (AML) that is …
chromosome 3q26 define an aggressive subtype of acute myeloid leukemia (AML) that is …
[HTML][HTML] PRMT5 regulates ATF4 transcript splicing and oxidative stress response
MM Szewczyk, GM Luciani, V Vu, A Murison… - Redox biology, 2022 - Elsevier
Abstract Protein methyltransferase 5 (PRMT5) symmetrically dimethylates arginine residues
leading to regulation of transcription and splicing programs. Although PRMT5 has emerged …
leading to regulation of transcription and splicing programs. Although PRMT5 has emerged …
[HTML][HTML] The PU. 1-modulated microRNA-22 is a regulator of monocyte/macrophage differentiation and acute myeloid leukemia
C Shen, MT Chen, XH Zhang, XL Yin, HM Ning… - PLoS …, 2016 - journals.plos.org
MicroRNA-22 (miR-22) is emerging as a critical regulator in organ development and various
cancers. However, its role in normal hematopoiesis and leukaemogenesis remains unclear …
cancers. However, its role in normal hematopoiesis and leukaemogenesis remains unclear …