Precursor T-Cell Lymphoblastic Leukemia-Lymphoma
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Ectopic overexpression of 10 NKL genes, of which six are unreported in T-ALL (NKX2-3, BARHL1, BARX2, EMX2, LBX2 and MSX2), was detectable in 17/104 (16%) T-ALLs.
|
28592888 |
2018 |
Malignant Neoplasms
|
0.010 |
AlteredExpression
|
group |
BEFREE |
Here we show that NKX2-3 is overexpressed in tumour cells from a subset of patients with marginal-zone lymphomas, but not with other B-cell malignancies.
|
27297662 |
2016 |
leukemia
|
0.010 |
Biomarker
|
disease |
BEFREE |
All together, our study defined a unique lncRNA expression signature associated with ETV6/RUNX1-positive BCP-ALL and identified lnc-RTN4R-1 and lnc-NKX2-3-1 as lncRNAs that might be functionally implicated in the biology of this prevalent subtype of human leukemia.
|
27650541 |
2016 |
Lymphoma
|
0.010 |
AlteredExpression
|
group |
BEFREE |
While Nkx2-3-deficient mice exhibit the absence of marginal-zone B cells, transgenic mice with expression of NKX2-3 in B cells show marginal-zone expansion that leads to the development of tumours, faithfully recapitulating the principal clinical and biological features of human marginal-zone lymphomas.
|
27297662 |
2016 |
Neoplasms
|
0.010 |
AlteredExpression
|
group |
BEFREE |
While Nkx2-3-deficient mice exhibit the absence of marginal-zone B cells, transgenic mice with expression of NKX2-3 in B cells show marginal-zone expansion that leads to the development of tumours, faithfully recapitulating the principal clinical and biological features of human marginal-zone lymphomas.
|
27297662 |
2016 |
Leukemogenesis
|
0.010 |
Biomarker
|
disease |
BEFREE |
This study implicates oncogenic NKX2-3 in lymphomagenesis, and provides a valid experimental mouse model for studying the biology and therapy of human marginal-zone B-cell lymphomas.
|
27297662 |
2016 |
Pelvic Organ Prolapse
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
There was 1 significantly down-regulated gene, NKX2-3 in patients with POP compared to the controls (p=4.28464e-013).
|
27521992 |
2016 |
Childhood Leukemia
|
0.010 |
Biomarker
|
disease |
BEFREE |
All together, our study defined a unique lncRNA expression signature associated with ETV6/RUNX1-positive BCP-ALL and identified lnc-RTN4R-1 and lnc-NKX2-3-1 as lncRNAs that might be functionally implicated in the biology of this prevalent subtype of human leukemia.
|
27650541 |
2016 |
Colorectal Carcinoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
Genes regulated by Nkx2-3 in sporadic and inflammatory bowel disease-associated colorectal cancer cell lines.
|
20165982 |
2010 |
Carcinogenesis
|
0.010 |
Biomarker
|
phenotype |
BEFREE |
Genes regulated by Nkx2-3 were grouped primarily within the following two functional categories: (1) immune and inflammatory response; and (2) cell proliferation, growth, and oncogenesis.
|
20165982 |
2010 |
Malignant neoplasm of colon and/or rectum
|
0.010 |
Biomarker
|
disease |
BEFREE |
Genes regulated by Nkx2-3 in sporadic and inflammatory bowel disease-associated colorectal cancer cell lines.
|
20165982 |
2010 |
Celiac Disease
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
We aimed to study the implication of five polymorphisms in these genes in CD susceptibility: rs10883365 and rs888208 in the NKX2-3 gene, rs2241880 in ATG16L1, and rs10065172 and rs4958847 in IRGM.
|
19683022 |
2009 |
Carcinoma, Neuroendocrine
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
However, chemokine C-X-C motif ligand 14 (CXCL14) and NK2 transcription factor related locus 3 Drosophila (NKX2-3) are expressed to a lower level in liver metastases than in primary tumors and normal enterochromaffin cells, which implies a role in neuroendocrine carcinoma differentiation.
|
18953328 |
2009 |
Secondary malignant neoplasm of liver
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
However, chemokine C-X-C motif ligand 14 (CXCL14) and NK2 transcription factor related locus 3 Drosophila (NKX2-3) are expressed to a lower level in liver metastases than in primary tumors and normal enterochromaffin cells, which implies a role in neuroendocrine carcinoma differentiation.
|
18953328 |
2009 |
Irritable Bowel Syndrome
|
0.020 |
GeneticVariation
|
disease |
BEFREE |
NKX2-3 variant rs11190140 is associated with IBD and alters binding of NFAT.
|
21803625 |
2012 |
Irritable Bowel Syndrome
|
0.020 |
GeneticVariation
|
disease |
BEFREE |
NKX2-3 and IRGM variants are associated with disease susceptibility to IBD in Eastern European patients.
|
21049557 |
2010 |
Inflammatory Bowel Diseases
|
0.090 |
AlteredExpression
|
group |
BEFREE |
Nkx2-3 as a transcriptional regulator of MAdCAM-1 controls vascular patterning in visceral lymphoid tissues in mice, and has been identified as a susceptibility factor for inflammatory bowel diseases in humans, associated with lymphoid neogenesis in the inflamed intestines.
|
30891037 |
2019 |
Inflammatory Bowel Diseases
|
0.090 |
GeneticVariation
|
group |
BEFREE |
Contribution of NKX2-3 polymorphisms to inflammatory bowel diseases: a meta-analysis of 35358 subjects.
|
24473197 |
2014 |
Inflammatory Bowel Diseases
|
0.090 |
GeneticVariation
|
group |
BEFREE |
We confirmed that the NKX2-3 polymorphism is associated with common susceptibility to IBD and that HLA-DRB1*0450 alleles increase susceptibility to CD but reduce risk for UC while HLA-DRB1*1502 alleles increase susceptibility to UC but reduce CD risk.
|
23942620 |
2014 |
Inflammatory Bowel Diseases
|
0.090 |
GeneticVariation
|
group |
BEFREE |
We speculate that the rs11190140 may regulate NKX2-3 expression and have a role in IBD pathogenesis.
|
21803625 |
2012 |
Inflammatory Bowel Diseases
|
0.090 |
Biomarker
|
group |
BEFREE |
To understand the cellular function of NKX2-3 and its potential role underlying IBD pathogenesis, we investigated the genes regulated by NKX2-3 in HIMEC using cDNA microarray.
|
21637825 |
2011 |
Inflammatory Bowel Diseases
|
0.090 |
GeneticVariation
|
group |
BEFREE |
Consistent with epidemiologic predictions, many IBD-associated loci demonstrate genome-wide significant associations to both CD and UC, notably, genes whose products function in the interleukin-23 pathway, and transcription factors, including NK2 transcription factor related, locus 3 (NKX2-3), SMAD3, STAT3, ZMIZ1, and c-REL.
|
21530736 |
2011 |
Inflammatory Bowel Diseases
|
0.090 |
AlteredExpression
|
group |
BEFREE |
Our present results demonstrate that a decrease in Nkx2-3 gene expression level can profoundly alter the expression of genes and cellular functions relevant to the pathogenesis and progression of IBD, such as EDN1.
|
20188614 |
2010 |
Inflammatory Bowel Diseases
|
0.090 |
Biomarker
|
group |
BEFREE |
The purpose of the current study is to determine genes regulated by Nkx2-3 in sporadic (CRS61) and inflammatory bowel disease-associated (CRS4) colorectal cancer cell lines.
|
20165982 |
2010 |
Inflammatory Bowel Diseases
|
0.090 |
GeneticVariation
|
group |
BEFREE |
NKX2-3 and IRGM are susceptibility loci for IBD in Eastern European patients.
|
21049557 |
2010 |