Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
To elucidate molecular mechanisms underpinning the tumor-promoting effects of GPNMB in this context, we interrogated activated pathways in tumors derived from the MMTV/Wnt-1 and MMTV/Wnt-1 × MMTV/GPNMB mice using RPPA analysis.
|
30914799 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Nephrometry score correlated with tumor proliferative activity inT1 clear cell renal cell carcinoma.
|
30826166 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Disruption of C3aR expression dampened tumour growth and the expression of Wnt-1, β-catenin and Sox-2 in the xenograft model.
|
30825266 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Wnt1-Late<sup>Ex</sup> tumors were enriched for activating <i>Hras1</i> mutations and were capable of reproducing tumors when serially transplanted into wild-type FVB female mice.
|
31213486 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Importantly, LBH inactivation in mammary epithelium significantly delayed tumor onset in MMTV-Wnt1 transgenic mice, with a median tumor-free survival of 32.5 weeks compared to 22.5 weeks in control LBH wild type MMTV-Wnt1 mice (p < 0.05).
|
30509497 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In mouse mammary tumors, we showed that Procr<sup>+</sup> cells are enriched for cancer stem cells (CSCs) in Wnt1 basal-like tumors, but not in Brca1 basal-like tumors or PyVT luminal tumors.
|
31481760 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Wnt-target genes are up-regulated in human intratumoral cDCs and decrease upon silencing Wnt1, accompanied by enhanced T cell cytotoxicity. siWnt1-nanoparticles given as single therapy or part of combinatorial immunotherapies act at both arms of the cancer-immune ecosystem to halt tumor growth.
|
30926812 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
To investigate molecular events associated with the loss of IGF-1R function in breast tumor cells, we inhibited IGF-1R in human cell lines using an IGF-1R blocking antibody and analyzed MMTV-Wnt1-mediated mouse tumors with reduced IGF-1R function through expression of a dominant-negative transgene.
|
30458886 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
WNT1 overexpression rescued the tumor suppressive effects of miR-329 in PTC cells.
|
30127962 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In conclusion, we found that miR-185 inhibits colon cancer cell proliferation and invasion by targeting Wnt1, and that it serves as a tumor suppressor, indicating that the modulation of miR-185 levels may potentially be therapeutic in colon cancer patients.
|
29454608 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Then, using the specific miRNA mimic and inhibitor, we proved that miR-152 impeded G<sub>1</sub>/S transition in the cell cycle of EECs and inhibited cellular proliferation via downregulating WNT-1 in mice and human endometrial cancer cell lines (Ishikawa, HEC-1-b, and KLE). miR-152 induced by P4 is an important inhibitor for the proliferation of EECs. miR-152 may be an important tumor suppressor microRNA in endometrial cancer.
|
28122483 |
2017 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
These data suggest that GRA inhibits the initiation and progression of gastric tumors by ameliorating the inflammatory microenvironment through downregulation of COX-2 expression and by inhibiting Wnt-1 expression through the upregulation of tumor suppressor miR-149-3p.
|
27713126 |
2016 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
When chemical carcinogens were employed during Wnt1-initiated mammary tumorigenesis, exposure to either 7,12-dimethylbenz(a)anthracene (DMBA) or N-ethyl-N-nitrosourea (ENU) dramatically accelerated tumor onset.
|
27207659 |
2016 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
We conclude that the frequently downregulated miR-148b can regulate WNT1/β-catenin signalling pathway and function as a tumor suppressor in HCC.
|
25627001 |
2015 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Recent studies demonstrate that Wnt or PORCN inhibitor, Wnt-C59, inhibits tumor growth in MMTV-WNT1 transgenic mice.
|
25980501 |
2015 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Subcutaneous injection of nude mice with Wnt1-overexpressing AGS cells resulted in larger tumors than injection of control AGS cells.
|
24481453 |
2014 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In this study, we compared FDG uptake in mammary tumors driven by the Akt1, c-MYC, HER2/neu, Wnt1, or H-Ras oncogenes in genetically engineered mice, correlating it to tumor growth, cell proliferation, and expression levels of gene involved in key steps of glycolytic metabolism.
|
25239452 |
2014 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
We demonstrate that Wnt ligands - Wnt1 and Wnt3a are expressed in a graded manner in these tumors as well as over-expressed in glioma stem cell-lines.
|
23337036 |
2013 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
However, individual Rspo2 and Wnt1 HC11 transfectants as well as the double transfectant were tumorigenic in athymic nude mice, with tumors from each line having distinctive histological characteristics.
|
21732367 |
2012 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
In this study, we show that doxycycline-dependent Wnt1 expression in subcutaneous and intracranial mouse glioma models induced endothelial Wnt/β-catenin signaling and led to diminished tumor growth, reduced vascular density, and normalized vessels with increased mural cell attachment.
|
22908324 |
2012 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
For model development, we characterized two cell lines, "mesenchymal (M)-Wnt" and "epithelial (E)-Wnt," derived from MMTV-Wnt-1 transgenic mouse mammary tumors.
|
22588949 |
2012 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Here, we show that, contrary to dogma, MMTV-Wnt1 mammary tumors with mutant p53 exhibited a superior clinical response compared to tumors with wild-type p53.
|
22698404 |
2012 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
The goal of this paper is to describe the role of the APC gene, and its derivatives, in the carcinogenicity pathway of WNT-1, identifying its role as a tumor suppressor gene in OSCC, while describing the genetic (loss of heterozygosity and mutations) and epigenetic alterations that modulate its expression and evaluate its relationship with the clinicopathological parameters of this type of tumors.
|
21937258 |
2012 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Exogenous E(2) "clamped" at early follicular and midluteal phase levels (i.e., 80 and 240 pg/ml) accelerated tumor formation in a dose-related fashion in ERKO/Wnt-1 animals (p = 0.0002).
|
20104523 |
2010 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
We finally revealed that induction of Wnt pathway cooperating with the prostaglandin E2 pathway in mice (K19-Wnt1/C2mE mice) further reproduce features of human gastric intestinal-type tumors.
|
20015407 |
2009 |