PBX1, PBX homeobox 1, 5087

N. diseases: 167; N. variants: 14
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1332977
Disease: Childhood Leukemia
Childhood Leukemia
0.100 AlteredExpression disease BEFREE For example, a recent study has shown that MTG16 can repress not only wild-type E2A-mediated transcription, but also leukemia fusion protein E2A-Pbx1-mediated transcription, suggesting that MTG16 may serve as a potential therapeutic target in acute lymphoblastic leukemia expressing the E2A-Pbx1 fusion protein. 29358956 2017
CUI: C1332977
Disease: Childhood Leukemia
Childhood Leukemia
0.100 GeneticVariation disease BEFREE Despite the induced expression of E2A-PBX1, no hematopoietic disease was observed, strongly suggesting that additional genetic alterations are required to develop leukemia. 27088431 2016
CUI: C1332977
Disease: Childhood Leukemia
Childhood Leukemia
0.100 Biomarker disease BEFREE This study thus suggests that RNF6 overexpression in leukemia is under the direction of PBX1 and that the PBX1/RNF6 axis can be developed as a novel therapeutic target of leukemia. 26971355 2016
CUI: C1332977
Disease: Childhood Leukemia
Childhood Leukemia
0.100 Biomarker disease BEFREE In preleukemic mice, conditional Pax5 deletion cooperated with E2A-PBX1 to expand progenitor B cell subpopulations, increasing penetrance and shortening leukemia latency. 26301816 2015
CUI: C1332977
Disease: Childhood Leukemia
Childhood Leukemia
0.100 GeneticVariation disease BEFREE We validated GIPFEL for the five most common gene fusions associated with childhood leukemia (MLL-AF4, MLL-AF9, MLL-ENL, ETV6-RUNX1, and TCF3-PBX1). 25137060 2014
CUI: C1332977
Disease: Childhood Leukemia
Childhood Leukemia
0.100 AlteredExpression disease BEFREE The observed in vitro and in vivo anti-leukemic potency of the αCD19-AON immunoconjugate provides the first preclinical proof-of-principle that t(1;19)(+) high risk B-lineage ALL can be treated with leukemia-specific biotherapeutic agents that knock-down E2A-PBX1 expression. 22990208 2013
CUI: C1332977
Disease: Childhood Leukemia
Childhood Leukemia
0.100 Biomarker disease BEFREE These results provide molecular insights into E-protein-driven differentiation of B-cells and the mechanism of E-protein silencing, and reveal the PCET/KIX interaction as a therapeutic target for E2A-PBX1-induced leukemia. 22972988 2012
CUI: C1332977
Disease: Childhood Leukemia
Childhood Leukemia
0.100 Biomarker disease BEFREE Namely, we have identified significant associations of overexpressed IGF2BP1 with ETV6/RUNX1-positive (r(2)=0.7891, y=0.8105x-0.4471, p<0.0001), underexpressed IGF2BP2 with E2A/PBX1-positive (p<0.01), and overexpressed IGF2BP2 and IGF2BP3 with MLL/AF4-positive (r(2)=0.6571, y=0.1507x-0.2722, p<0.0001, and r(2)=0.7022, y=0.6482x-0.7660, p<0.0001, respectively) leukemia. 21414819 2011
CUI: C1332977
Disease: Childhood Leukemia
Childhood Leukemia
0.100 Biomarker disease BEFREE Despite improvements in current combinational chemotherapy regimens, the prognosis of the (1;19)(q23;p13) translocation (E2A/PBX1)-positive B-cell precursor acute lymphoblastic leukemia (ALL) is poor in pediatric leukemia patients. 19922767 2010
CUI: C1332977
Disease: Childhood Leukemia
Childhood Leukemia
0.100 Biomarker disease BEFREE Lessons from the analysis of children with TCF3-PBX1 ALL could help to identify treatment components essential for this leukemia subtype. 18024406 2007
CUI: C1332977
Disease: Childhood Leukemia
Childhood Leukemia
0.100 AlteredExpression disease BEFREE Targeted-E2A-PBX1 inhibition leads to reduced expression of the EB-1 and Wnt16b genes; aberrant expression of these genes may be a key step in leukemogenesis in t(1;19)-positive pre-B leukemia. 16769578 2006
CUI: C1332977
Disease: Childhood Leukemia
Childhood Leukemia
0.100 Biomarker disease BEFREE Seven distinct leukemia subtypes were identified representing known leukemia subtypes including: BCR-ABL, E2A-PBX1, TEL-AML1, rearrangements in the MLL gene, hyperdiploid karyotype (i.e., > 50 chromosomes), and T-ALL as well as a new leukemia subtype. 14633779 2003
CUI: C1332977
Disease: Childhood Leukemia
Childhood Leukemia
0.100 AlteredExpression disease BEFREE Since the E2A, PBX1 and HLF proteins all appear to function as transcription factors, it appears likely that the oncogenic fusion proteins contribute to leukemia development by causing abnormal transcriptional regulation of key target genes. 12700034 2003
CUI: C1332977
Disease: Childhood Leukemia
Childhood Leukemia
0.100 Biomarker disease BEFREE The prenatal origin of the leukemia was assessed in 15 pediatric patients by screening for the clonotypic E2A-PBX1 translocation in neonatal blood spots, or Guthrie cards, obtained from the children at the time of birth. 12415113 2002
CUI: C1332977
Disease: Childhood Leukemia
Childhood Leukemia
0.100 Biomarker disease BEFREE Oncogenic homeodomain transcription factor E2A-Pbx1 activates a novel WNT gene in pre-B acute lymphoblastoid leukemia. 10500199 1999
CUI: C1332977
Disease: Childhood Leukemia
Childhood Leukemia
0.100 Biomarker disease BEFREE Pbx1 is converted into a transcriptional activator upon acquiring the N-terminal region of E2A in pre-B-cell acute lymphoblastoid leukemia. 8327485 1993