Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
DLK1 overexpression or knockdown was achieved by adenovirus gene delivery to evaluate the effect of DLK1 on the oncogenic behaviors in ovarian cancer cells and in xenografted tumors.
|
30626939 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
DLK1 was abnormally expressed in a variety of tumors, affecting tumorigenesis and developments.
|
31661545 |
2019 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
We discovered that Snail mediated the downregulation of the imprinted Dlk1-Dio3 locus, a complex genomic region containing protein-coding genes and non-coding RNAs that has been linked to tumor malignancy in lung cancer patients.
|
30190790 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
DLK1 has been linked to various tumors and associated with tumor stem cell features.
|
30144579 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Further, a large number of miRs observed in tumour network mapped to a specific chromosomal location in DLK1-DIO3 (Chr14q32); some of those miRs have also been associated with EMT and MET regulation.
|
29051564 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Vaccines targeting both DLK1 and DLK2 resulted in superior antitumor benefits in association with improved activation and recruitment of antigen-specific Type 1 CD8<sup>+</sup> T cells, reduced presence of myeloid-derived suppressive cells, T regulatory cell and tumor vascular normalization.
|
28405524 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In this work, we focused on the role of DLK1 in the control of breast cancer cell growth, a tumor type in which NOTCH receptors have been shown to play both opposite roles.
|
28461338 |
2017 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
The cluster of microRNAs (miRNAs) in the DLK1-DIO3 genomic imprinted region contains several miRNAs that have a significant regulatory role in tumor proliferation and invasion.
|
28043921 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Human HCC tissue showed overexpression of IMP2, which strongly correlated with the fetal markers AFP and DLK1/Pref-1/FA-1 and was particularly elevated in tumors with stem-like features and hypervascularization.
|
26426686 |
2015 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
The analyses revealed the involvement of both coding and non coding RNAs (SNORDs located in DLK1-DIO3 region) and support a model of stepwise progression mainly driven by epigenetic changes involving tumour vascular supply and tumoral cellular component.
|
25115389 |
2014 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Dlk1 is paternally expressed and belongs to a group of imprinted genes associated with rhabdomyosarcomas but not with other primitive childhood tumors to date.
|
23577150 |
2013 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
We identified strong induction of Retrotransposon-like 1 (Rtl1) expression as the only consistent alteration detected in all SB-induced tumors with Dlk1-Dio3 integrations, suggesting that Rtl1 activation serves as a driver of HCC.
|
23593033 |
2013 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Immortalized fibroblastic 3T3 cells can grow into tumors in nude mice but the size of tumors are smaller from those overexpressing DLK1.
|
22513084 |
2012 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
Given that the reduced expression of genes within the DLK1-MEG3 locus and the HOX loci is associated with MEN1-like sporadic tumors, our data suggests a possible role for menin-dependent H3K4me3 at these genes in the initiation and progression of sporadic pancreatic endocrine tumors.
|
22666422 |
2012 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
The growth suppression by miRNAs in PDFS cells is consistent with the hypothesis that the DLK1-MEG3 locus plays a tumor suppressor role in human NFAs.
|
21871428 |
2011 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Our objectives were 1) to investigate cell-type- and tumor-type-specific expression of MEG3 in the human pituitary and 2) to investigate whether methylation in the intergenic differentially methylated region (IG-DMR) at the DLK1/MEG3 locus is involved in the loss of MEG3 expression in tumors.
|
18628527 |
2008 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
Last, eight miRNAs located in the chromosome 14 miRNA cluster (Dlk1-Gtl2 domain) were identified as potential tumor suppressor genes.
|
18458333 |
2008 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Using RT-PCR, western blotting and immunohistochemistry, we analyzed the expression of DLK1 in the tumor samples and evaluated the results statistically.
|
18352842 |
2008 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
These data suggest that DLK1 as an imprinted gene could be significantly up-regulated in HCC due to certain epigenetic events and contribute to the oncogenesis of this tumor.
|
17114643 |
2007 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Imprinted DLK1 is a putative tumor suppressor gene and inactivated by epimutation at the region upstream of GTL2 in human renal cell carcinoma.
|
16439445 |
2006 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Moderate to high expression of DLK1 was detected by Q-PCR in nine of 13 tumours with myogenic differentiation.
|
15677533 |
2005 |
Neoplasms
|
0.100 |
PosttranslationalModification
|
group |
BEFREE |
Epigenetic alteration at the DLK1-GTL2 imprinted domain in human neoplasia: analysis of neuroblastoma, phaeochromocytoma and Wilms' tumour.
|
15798773 |
2005 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Furthermore, higher dlk protein expression in the tumor endothelium than in the endothelium of normal adrenal gland implies that dlk may regulate the endothelial function in neuroblastic tumors.
|
15605081 |
2005 |