Role of RUNX1 in hematological malignancies

R Sood, Y Kamikubo, P Liu - … Journal of the American Society of …, 2017 - ashpublications.org
RUNX1 is a member of the core-binding factor family of transcription factors and is
indispensable for the establishment of definitive hematopoiesis in vertebrates. RUNX1 is …

[HTML][HTML] Pathogenesis of ETV6/RUNX1-positive childhood acute lymphoblastic leukemia and mechanisms underlying its relapse

C Sun, L Chang, X Zhu - Oncotarget, 2017 - ncbi.nlm.nih.gov
Abstract ETV6/RUNX1 (E/R) is the most common fusion gene in childhood acute
lymphoblastic leukemia (ALL). Multiple lines of evidence imply a “two-hit” model for the …

SLX4IP antagonizes promiscuous BLM activity during ALT maintenance

S Panier, M Maric, G Hewitt, E Mason-Osann, H Gali… - Molecular cell, 2019 - cell.com
Cancer cells acquire unlimited proliferative capacity by either re-expressing telomerase or
inducing alternative lengthening of telomeres (ALT), which relies on telomere …

Acute lymphoblastic leukemia

CJ Harrison, B Johansson - … Cytogenetics: Chromosomal and …, 2015 - Wiley Online Library
Acute lymphoblastic leukemia (ALL) is classified as B‐lineage ALL (B‐ALL) and T‐lineage
ALL (T‐ALL). The incidence of ALL is almost three times higher in white than black children …

Clonal origins of relapse in ETV6-RUNX1 acute lymphoblastic leukemia

FW Van Delft, S Horsley, S Colman… - Blood, The Journal …, 2011 - ashpublications.org
B-cell precursor childhood acute lymphoblastic leukemia with ETV6-RUNX1 (TEL-AML1)
fusion has an overall good prognosis, but relapses occur, usually after cessation of …

Modeling the evolution of ETV6-RUNX1–induced B-cell precursor acute lymphoblastic leukemia in mice

L van der Weyden, G Giotopoulos… - Blood, The Journal …, 2011 - ashpublications.org
Abstract The t (12; 21) translocation that generates the ETV6-RUNX1 (TEL-AML1) fusion
gene, is the most common chromosomal rearrangement in childhood cancer and is …

The landscape of secondary genetic rearrangements in pediatric patients with B-cell acute lymphoblastic leukemia with t (12; 21)

A Kaczmarska, J Derebas, M Pinkosz, M Niedźwiecki… - Cells, 2023 - mdpi.com
The most frequent chromosomal rearrangement in childhood B-cell acute lymphoblastic
leukemia (B-ALL) is translocation t (12; 21)(p13; q22). It results in the fusion of the ETV6 …

Ikaros and leukaemia

L Olsson, B Johansson - British journal of haematology, 2015 - Wiley Online Library
The IKZF 1 gene at 7p12. 2 codes for IKAROS (also termed IKZF 1), an essential
transcription factor in haematopoiesis involved primarily in lymphoid differentiation. Its …

Molecular and pharmacological heterogeneity of ETV6::RUNX1 acute lymphoblastic leukemia

Z Li, H Zhao, W Yang, M Maillard, S Yoshimura… - Nature …, 2025 - nature.com
Abstract ETV6:: RUNX1 is the most common fusion gene in childhood acute lymphoblastic
leukemia (ALL) associated with favorable prognosis, but the optimal therapy for this subtype …

ETV6/RUNX1 induces reactive oxygen species and drives the accumulation of DNA damage in B cells

HP Kantner, W Warsch, A Delogu, E Bauer… - Neoplasia, 2013 - Elsevier
Abstract The t (12; 21)(p13; q22) chromosomal translocation is the most frequent
translocation in childhood B cell precursor-acute lymphoblastic leukemia and results in the …