Neoplasms
|
0.060 |
Biomarker
|
group |
BEFREE |
Tumor xenograft models were established for investigating the effect of CLEC14A on tumor formation.
|
30191970 |
2019 |
Neoplasms
|
0.060 |
AlteredExpression
|
group |
BEFREE |
The C-type lectin domain containing group 14 family members CLEC14A and CD93 are proteins expressed by endothelium and are implicated in tumour angiogenesis.
|
28671670 |
2017 |
Neoplasms
|
0.060 |
Biomarker
|
group |
BEFREE |
Implanted tumor growth was profoundly reduced in CLEC14A-KO mice compared with that seen in WT littermates, but tumor-bearing CLEC14A-KO mice died sooner.
|
27991863 |
2017 |
Neoplasms
|
0.060 |
Biomarker
|
group |
BEFREE |
CLEC14a (C-type lectin domain family 14 member) is a tumor endothelial cell marker protein that is known to play an important role in tumor angiogenesis, but the basic molecular mechanisms underlying this function have not yet been clearly elucidated.
|
28878328 |
2017 |
Neoplasms
|
0.060 |
Biomarker
|
group |
BEFREE |
We conclude that CLEC14A-MMRN2 binding has a role in inducing sprouting angiogenesis during tumour growth, which has the potential to be manipulated in future antiangiogenic therapy design.
|
25745997 |
2015 |
Neoplasms
|
0.060 |
AlteredExpression
|
group |
BEFREE |
CLEC14A overexpression in tumor vessels was seen in a wide range of solid tumor types.
|
21706054 |
2012 |
Tumor Angiogenesis
|
0.030 |
Biomarker
|
phenotype |
BEFREE |
These findings suggest that antibody targeting of CLEC14a-CTLD has the potential to suppress VEGF-dependent angiogenesis and tumor angiogenesis and that CLEC14a-CTLD may be a novel anti-angiogenic target for VEGF-dependent angiogenesis and tumor angiogenesis.
|
29316206 |
2018 |
Tumor Angiogenesis
|
0.030 |
Biomarker
|
phenotype |
BEFREE |
We suggest that CLEC14A may be a more specific endothelial marker to assess tumor angiogenesis.
|
27567920 |
2017 |
Tumor Angiogenesis
|
0.030 |
Biomarker
|
phenotype |
BEFREE |
CLEC14a (C-type lectin domain family 14 member) is a tumor endothelial cell marker protein that is known to play an important role in tumor angiogenesis, but the basic molecular mechanisms underlying this function have not yet been clearly elucidated.
|
28878328 |
2017 |
Malignant Neoplasms
|
0.010 |
AlteredExpression
|
group |
BEFREE |
Activin receptor-like kinase 1 is associated with immune cell infiltration and regulates CLEC14A transcription in cancer.
|
30132150 |
2019 |
Adenocarcinoma of lung (disorder)
|
0.010 |
PosttranslationalModification
|
disease |
BEFREE |
Overexpressing CLEC14A or inhibiting the methylation level of CLEC14A in A549 and LTEP-a-2 cells impeded the duplication of LUAD cells, promoted apoptosis, attenuated cell migration, and invasion ability, and arrested cell cycle at the G0/G1 phase.
|
30191970 |
2019 |
Carcinogenesis
|
0.010 |
AlteredExpression
|
phenotype |
BEFREE |
Overexpression of CLEC14A inhibited tumorigenesis of LUAD cells in nude mice.
|
30191970 |
2019 |
Primary malignant neoplasm
|
0.010 |
AlteredExpression
|
group |
BEFREE |
Activin receptor-like kinase 1 is associated with immune cell infiltration and regulates CLEC14A transcription in cancer.
|
30132150 |
2019 |
Pancreatic carcinoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
CLEC14A and CD248 can bind MMRN2 simultaneously and this occurs at the interface between endothelium and pericytes in human pancreatic cancer.
|
28671670 |
2017 |
Malignant neoplasm of pancreas
|
0.010 |
Biomarker
|
disease |
BEFREE |
CLEC14A and CD248 can bind MMRN2 simultaneously and this occurs at the interface between endothelium and pericytes in human pancreatic cancer.
|
28671670 |
2017 |
Epithelial ovarian cancer
|
0.010 |
Biomarker
|
disease |
BEFREE |
This study demonstrates MVD as detected by CLEC14A in EOC.
|
27567920 |
2017 |
Carcinoma, Ovarian Epithelial
|
0.010 |
Biomarker
|
disease |
BEFREE |
This study demonstrates MVD as detected by CLEC14A in EOC.
|
27567920 |
2017 |
melanoma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Reverse-phase protein array analysis of phospho-proteomic changes in mutant NRAS melanoma in response to trametinib indicated a compensatory increase in v-akt murine thymoma viral oncogene homolog signaling and decreased expression of mitogen-inducible gene 6 (MIG6), a negative regulator of epidermal growth factor receptor/v-erb-b2 erythroblastic leukemia viral oncogene homolog receptors.
|
26967478 |
2016 |
Thymoma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Reverse-phase protein array analysis of phospho-proteomic changes in mutant NRAS melanoma in response to trametinib indicated a compensatory increase in v-akt murine thymoma viral oncogene homolog signaling and decreased expression of mitogen-inducible gene 6 (MIG6), a negative regulator of epidermal growth factor receptor/v-erb-b2 erythroblastic leukemia viral oncogene homolog receptors.
|
26967478 |
2016 |
IGA Glomerulonephritis
|
0.010 |
Biomarker
|
disease |
BEFREE |
After each patient with IgA nephropathy was randomly matched to a non-CKD participant on age (±5 years), gender, mean arterial pressure (±5 mmHg) and eGFR (±5 mL/min/1.73 m(2)), a multivariate conditional logistic regression model also verified their significant association [odds ratio 0.42 (95% confidence interval 0.18-1.00) and odds ratio 0.09 (95% confidence interval 0.01-0.73), P(trend) = 0.004].
|
21737517 |
2012 |
tumor vasculature
|
0.010 |
AlteredExpression
|
phenotype |
BEFREE |
Finally, in endothelial cultures, expression of CLEC14A increased at low shear stress, and we hypothesize that low shear stress due to poor blood flow in the disorganized tumor vasculature induces expression of CLEC14A on tumor vessels and pro-angiogenic phenotypes.
|
21706054 |
2012 |
Malignant neoplasm of breast
|
0.010 |
Biomarker
|
disease |
BEFREE |
Finally, SLC16A12, GALR2, TOX, SPOCK2, EGFR5 and DPYS are candidate biomarkers for breast cancer (methylation range 33%-79%) with the combination of EGFR5 or TOX hypermethylation showing a sensitivity of 92% and specificity of 92%.
|
18446232 |
2008 |
Breast Carcinoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
Finally, SLC16A12, GALR2, TOX, SPOCK2, EGFR5 and DPYS are candidate biomarkers for breast cancer (methylation range 33%-79%) with the combination of EGFR5 or TOX hypermethylation showing a sensitivity of 92% and specificity of 92%.
|
18446232 |
2008 |