Neuroblastoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
Taken together, these results demonstrated the tumor suppressive role of miR-144-3p in NB and may advance the understanding of the underlying mechanisms of miR-144-3p and HOXA7 in NB.
|
30720179 |
2019 |
Central neuroblastoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
Taken together, these results demonstrated the tumor suppressive role of miR-144-3p in NB and may advance the understanding of the underlying mechanisms of miR-144-3p and HOXA7 in NB.
|
30720179 |
2019 |
Precursor T-Cell Lymphoblastic Leukemia-Lymphoma
|
0.010 |
PosttranslationalModification
|
disease |
BEFREE |
An integrated transcriptome analysis in T-cell acute lymphoblastic leukemia links DNA methylation subgroups to dysregulated TAL1 and ANTP homeobox gene expression.
|
30575306 |
2019 |
Childhood Neuroblastoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
Taken together, these results demonstrated the tumor suppressive role of miR-144-3p in NB and may advance the understanding of the underlying mechanisms of miR-144-3p and HOXA7 in NB.
|
30720179 |
2019 |
Malignant Neoplasms
|
0.010 |
AlteredExpression
|
group |
BEFREE |
HOXA7 expression was higher in patients with stage III and IV cancer than in patients with stage I and II cancer (P < 0.05).
|
28529281 |
2017 |
Glioma
|
0.010 |
Biomarker
|
disease |
BEFREE |
CD133 (p = 0.021) and HOXA7 (p = 0.001) were independent prognostic markers when the three glioma patient cohorts were combined (n = 231).
|
28055976 |
2017 |
Prostatic Neoplasms
|
0.010 |
AlteredExpression
|
group |
BEFREE |
We identified 255 genes that were deregulated in prostate tumors compared with BPH tissues. qRT-PCR was conducted to examine the expression levels of the four genes in FNA biopsies and confirmed that ITGBL1 was significantly up-regulated and HOXA7, KRT15 and TGM4 were down-regulated in the PCa compared to the BPH, with a sensitivity of 87.1% and a specificity of 87.8%; the area under the receiver operating characteristic curve was estimated at 0.94, which was significantly improved compared with PSA alone (AUC = 0.82).
|
29285211 |
2017 |
Primary malignant neoplasm
|
0.010 |
AlteredExpression
|
group |
BEFREE |
HOXA7 expression was higher in patients with stage III and IV cancer than in patients with stage I and II cancer (P < 0.05).
|
28529281 |
2017 |
Benign Prostatic Hyperplasia
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
We identified 255 genes that were deregulated in prostate tumors compared with BPH tissues. qRT-PCR was conducted to examine the expression levels of the four genes in FNA biopsies and confirmed that ITGBL1 was significantly up-regulated and HOXA7, KRT15 and TGM4 were down-regulated in the PCa compared to the BPH, with a sensitivity of 87.1% and a specificity of 87.8%; the area under the receiver operating characteristic curve was estimated at 0.94, which was significantly improved compared with PSA alone (AUC = 0.82).
|
29285211 |
2017 |
Adult Liver Carcinoma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Moreover, higher expression level of HOXA7 was associated with poorer prognosis of liver cancer patients.
|
27600149 |
2016 |
Liver and Intrahepatic Biliary Tract Carcinoma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Moreover, higher expression level of HOXA7 was associated with poorer prognosis of liver cancer patients.
|
27600149 |
2016 |
Malignant neoplasm of liver
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Moreover, higher expression level of HOXA7 was associated with poorer prognosis of liver cancer patients.
|
27600149 |
2016 |
Secondary malignant neoplasm of liver
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
First, increased levels of HOXA7 were examined in liver cancer especially in metastatic liver cancer.
|
27600149 |
2016 |
Leukemogenesis
|
0.010 |
Biomarker
|
disease |
BEFREE |
In the current study, we identified Hoxa7, Hoxa9 and Hox cofactor Meis1 as AP-2α target genes, which are involved in myeloid leukemogenesis.
|
23660297 |
2013 |
Meningioma
|
0.010 |
PosttranslationalModification
|
disease |
BEFREE |
This study demonstrates that HOXA7, 9, and 10 are methylation targets in meningioma, associated with histopathology and clinical aggressiveness parameters.
|
22735029 |
2012 |
Meningiomas, Multiple
|
0.010 |
Biomarker
|
disease |
BEFREE |
Moreover, in newly diagnosed WHO I meningiomas, HOXA7, 9, and 10 methylation was significantly lower than in WHO I samples derived from recurring tumors, and multiple meningiomas presented significantly higher HOXA 10 methylation with respect to solitary meningiomas.
|
22735029 |
2012 |
Adult Meningioma
|
0.010 |
PosttranslationalModification
|
disease |
BEFREE |
This study demonstrates that HOXA7, 9, and 10 are methylation targets in meningioma, associated with histopathology and clinical aggressiveness parameters.
|
22735029 |
2012 |
Meningioma, benign, no ICD-O subtype
|
0.010 |
PosttranslationalModification
|
disease |
BEFREE |
This study demonstrates that HOXA7, 9, and 10 are methylation targets in meningioma, associated with histopathology and clinical aggressiveness parameters.
|
22735029 |
2012 |
Mammary Neoplasms
|
0.010 |
PosttranslationalModification
|
group |
BEFREE |
Aberrant methylation and associated gene silencing was observed for Hoxa7, a gene that is differentially methylated in human breast tumors, and Gata2, a novel candidate gene.
|
21373886 |
2011 |
Adenocarcinoma
|
0.010 |
AlteredExpression
|
group |
BEFREE |
They included HOXA4 and HOXA7 because, by cDNA microarray analysis, these were more highly expressed in invasive ovarian carcinomas than in benign or borderline (noninvasive) ovarian tumors, and HOXA9 because it characterizes normal oviductal epithelium, which resembles ovarian serous adenocarcinomas.
|
19281776 |
2009 |
Carcinoma
|
0.010 |
Biomarker
|
group |
BEFREE |
There were significant associations of strong HOXA7 staining of stroma and tumor nuclei with the clear cell histotype (stroma: P = .0022, nuclei: P = .0003) and of weak/absent staining with serous carcinomas.
|
17959889 |
2007 |
Benign Neoplasm
|
0.010 |
AlteredExpression
|
group |
BEFREE |
HOXA7 mRNA expression was higher in carcinomas than in benign tumors.
|
17959889 |
2007 |
Epithelial ovarian cancer
|
0.010 |
Biomarker
|
disease |
BEFREE |
HOXA7 in epithelial ovarian cancer: interrelationships between differentiation and clinical features.
|
17959889 |
2007 |
granulosa cell tumor
|
0.010 |
Biomarker
|
disease |
BEFREE |
We generated a thoroughly characterized polyclonal rabbit antibody against human HOXA7 and used it to study the distribution, role, and regulation of HOXA7 in human ovarian folliculogenesis and in granulosa cell tumors.
|
16466395 |
2006 |
Werner Syndrome
|
0.010 |
Biomarker
|
disease |
BEFREE |
Gene expression changes that were common to all three cell types included up-regulation of GCK (glucokinase), CS (citrate synthase), HOX1 (heme oxygenase 1), CKMT2 (mitochondrial creatine kinase 2), MYC (v-myc myelocytomatosis viral oncogene homolog), and WRN (Werner syndrome helicase), and down-regulation of FBP1 (fructose-1, 6-bisphosphatase 1) and COL4A1 (collagen, type IV, alpha 1).
|
15561107 |
2005 |