Neoplasms
|
0.020 |
Biomarker
|
group |
BEFREE |
Furthermore, EFL2 inhibited tumor growth and STAT3 phosphorylation in vivo.
|
31085375 |
2019 |
Liver carcinoma
|
0.020 |
Biomarker
|
disease |
BEFREE |
EFL2 also suppressed the cell migration and colony formation of hepatocellular carcinoma cells.
|
31085375 |
2019 |
Neoplasms
|
0.020 |
Biomarker
|
group |
BEFREE |
The results indicated that EFNA3 serves as a tumor suppressor in MPNST cells and it may play a critical role in the focal adhesion kinase (FAK) signaling and VEGF-associated tumor angiogenesis pathway.
|
25955218 |
2015 |
Carcinogenesis
|
0.020 |
Biomarker
|
phenotype |
BEFREE |
Our previous study indicated that miR-210-mediated Ephrin-A3 (EFNA3) promotion of proliferation and invasion of MPNST cells plays an important role in MPNST tumorigenesis and progression.
|
25955218 |
2015 |
Malignant Peripheral Nerve Sheath Tumor
|
0.020 |
Biomarker
|
disease |
BEFREE |
The results indicated that EFNA3 serves as a tumor suppressor in MPNST cells and it may play a critical role in the focal adhesion kinase (FAK) signaling and VEGF-associated tumor angiogenesis pathway.
|
25955218 |
2015 |
Carcinogenesis
|
0.020 |
Biomarker
|
phenotype |
BEFREE |
These results suggest that miR-210-mediated EFNA3 promotion of proliferation and invasion of MPNST cells plays an important role in MPNST tumorigenesis and progression. miR-210 and EFNA3 may be candidate novel therapeutic targets for MPNST.
|
24512729 |
2013 |
Malignant Peripheral Nerve Sheath Tumor
|
0.020 |
Biomarker
|
disease |
BEFREE |
These results suggest that miR-210-mediated EFNA3 promotion of proliferation and invasion of MPNST cells plays an important role in MPNST tumorigenesis and progression. miR-210 and EFNA3 may be candidate novel therapeutic targets for MPNST.
|
24512729 |
2013 |
Liver carcinoma
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
Ephrin-A3 was up-regulated 26-fold in lung cancer, and EphB2 was up-regulated 9-fold in hepatocellular carcinoma.
|
14726470 |
2004 |
Adrenal Gland Pheochromocytoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
In the current study, the functions of lncRNA EFNA3 on hypoxia-injured rat adrenal pheochromocytoma (PC-12) cells and the underlying molecular mechanism were studied.
|
30125989 |
2019 |
Machado-Joseph Disease
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
This increased expression of Efna3 was recapitulated in Atxn3 knockout mouse brainstem, a selectively vulnerable brain region in SCA3.
|
30231063 |
2018 |
Hemangiosarcoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
Knockdown of E2F3 or ephrin A3 resulted in a significant decrease in the number of angiosarcoma cells.
|
28739548 |
2017 |
Myocardial Infarction
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
In conclusion, MSC-EVs are sufficient to improve angiogenesis and exert therapeutic effect on MI, its pro- angiogenesis effect might be associated with a miR-210-Efna3 dependent mechanism.
|
28249798 |
2017 |
Adult Angiosarcoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
Knockdown of E2F3 or ephrin A3 resulted in a significant decrease in the number of angiosarcoma cells.
|
28739548 |
2017 |
Childhood Angiosarcoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
Knockdown of E2F3 or ephrin A3 resulted in a significant decrease in the number of angiosarcoma cells.
|
28739548 |
2017 |
Malignant neoplasm of breast
|
0.010 |
Biomarker
|
disease |
BEFREE |
Taken together, our results suggest that hypoxia could contribute to metastatic spread of breast cancer via HIF-mediated induction of EFNA3 lncRNAs and subsequent Ephrin-A3 protein accumulation.
|
25023702 |
2015 |
Medulloblastoma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
We found EPHB4 and EFNA4 almost exclusively expressed by SHH MB, whereas EPHA2, EPHA8, EFNA1 and EFNA3 are predominantly expressed by non-SHH MB.
|
25258252 |
2015 |
Childhood Medulloblastoma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
We found EPHB4 and EFNA4 almost exclusively expressed by SHH MB, whereas EPHA2, EPHA8, EFNA1 and EFNA3 are predominantly expressed by non-SHH MB.
|
25258252 |
2015 |
Adult Malignant Peripheral Nerve Sheath Tumor
|
0.010 |
Biomarker
|
disease |
BEFREE |
Dissecting the roles of Ephrin-A3 in malignant peripheral nerve sheath tumor by TALENs.
|
25955218 |
2015 |
Adult Medulloblastoma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
We found EPHB4 and EFNA4 almost exclusively expressed by SHH MB, whereas EPHA2, EPHA8, EFNA1 and EFNA3 are predominantly expressed by non-SHH MB.
|
25258252 |
2015 |
Childhood Malignant Peripheral Nerve Sheath Tumor
|
0.010 |
Biomarker
|
disease |
BEFREE |
Dissecting the roles of Ephrin-A3 in malignant peripheral nerve sheath tumor by TALENs.
|
25955218 |
2015 |
Breast Carcinoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
Taken together, our results suggest that hypoxia could contribute to metastatic spread of breast cancer via HIF-mediated induction of EFNA3 lncRNAs and subsequent Ephrin-A3 protein accumulation.
|
25023702 |
2015 |
Tumor Angiogenesis
|
0.010 |
Biomarker
|
phenotype |
BEFREE |
The results indicated that EFNA3 serves as a tumor suppressor in MPNST cells and it may play a critical role in the focal adhesion kinase (FAK) signaling and VEGF-associated tumor angiogenesis pathway.
|
25955218 |
2015 |
neurofibroma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
In this study, miR-210 was identified as downregulated in MPNST cells, and its potential target ephrin-A3 (EFNA3) was upregulated in them compared with neurofibroma cells using quantitative real-time (qRT)-PCR.
|
24512729 |
2013 |
Non-Small Cell Lung Carcinoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
Our pilot study identified upregulated genes in early-stage NSCLC including growth factors (TGFA and EFNA3), the adhesion molecule THBS2, cytokines and chemokines (MDK, CXCL9, CXCL10), and the serine protease PLAU.
|
21528670 |
2011 |
Anoxia
|
0.010 |
Biomarker
|
phenotype |
LHGDN |
We determined that one relevant target of miR-210 in hypoxia was Ephrin-A3 since miR-210 was necessary and sufficient to down-modulate its expression.
|
18417479 |
2008 |