Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Thus, targeting fibroblasts or PDGF-D-induced signals may represent an effective tool to block tumor-associated lymphangiogenesis and reduce the invasiveness of cholangiocarcinoma.
|
30553841 |
2019 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
As a result, we subsequently examined 16 additional cases of primary breast dermatofibrosarcoma protuberans, identifying 2 additional tumors with PDGFD rearrangement.
|
30014607 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Down-regulation of PDGF-D inhibited the tumor growth, migration and angiogenesis of SW480 cells in vitro and in vivo.
|
28035069 |
2017 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Analysis of the β-PDGFR ligands in PCa revealed association between PDGF-D expression and Gleason score as well as tumor stage.
|
26157007 |
2016 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Both in vitro and in vivo experiments showed PDGF-D could promote tumor growth and invasion through up-regulating MMP2/9 and inducing EMT.
|
24646915 |
2014 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Substantial evidence has demonstrated that platelet-derived growth factor-D (PDGF-D) is tightly associated with the development and progression of tumors.
|
23187740 |
2013 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In conclusion, our data show that tissue-resident stem cells interact with the cancer microenvironment via PDGF-D, induce EMT in the cancer cells in a paracrine fashion, thereby increasing the number of cancer stem cells and increase tumor growth in a PDGF dependent manner.
|
22038895 |
2012 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Since NF-κB activation plays a crucial role in Notch signaling as well as in epithelial-mesenchymal transition and tumor aggressiveness, we determined the DNA binding activity of NF-κB and our findings are consistent showing that PDGF-D over-expression led to increased DNA binding activity of NF-κB while it was found to be decreased by inactivation of PDGF-D.
|
20379844 |
2011 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Several genes involved in cell adhesion (CD44, LOX), cell division (CKS2, BIRC5 and UBE2C), cell differentiation (Notch1) or signal transduction (ARHGAP28) were upregulated, whereas tumour suppressor genes (LR1B, DRR1, PLZF, GPX3, SYNPO, TIMP3 and HOPS) and genes involved in cell adhesion (PROS1), proliferation (SERPINF1 and PDGFD) and differentiation (AOX1) were downregulated in groups B and C compared to group A.
|
19885562 |
2009 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
These results provided a novel mechanism by which PDGF-D promotes EMT, which in turn increases tumor growth, and these results further suggest that PDGF-D could be a novel therapeutic target for the prevention and/or treatment of prostate cancer.
|
18403754 |
2008 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Overexpression of PDGF-D in SN12-C cells promoted tumor growth, angiogenesis, and metastasis of human renal cell carcinoma in an orthotopic severe combined immunodeficient (SCID) mouse model.
|
15994946 |
2005 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In summary, these results suggest that PDGF-D induce cellular transformation and promote tumour growth by accelerating the proliferation rate of the tumour cells, and by stimulation of tumour neovascularization.
|
12629513 |
2003 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
PDGF D transforming ability and tumor formation in SCID mice was further demonstrated.
|
11980634 |
2002 |