Carcinoma
|
0.300 |
Biomarker
|
group |
CTD_human |
In primary mammary carcinomas, five (Angptl4, Coro1a, RGD1304982, Tmem37 and Ndn) of the 29 genes were methylated in one or more of 25 samples.
|
21489049 |
2011 |
Animal Mammary Neoplasms
|
0.300 |
Biomarker
|
phenotype |
CTD_human |
Methylation silencing of angiopoietin-like 4 in rat and human mammary carcinomas.
|
21489049 |
2011 |
Anaplastic carcinoma
|
0.300 |
Biomarker
|
disease |
CTD_human |
Methylation silencing of angiopoietin-like 4 in rat and human mammary carcinomas.
|
21489049 |
2011 |
Carcinoma, Spindle-Cell
|
0.300 |
Biomarker
|
disease |
CTD_human |
Methylation silencing of angiopoietin-like 4 in rat and human mammary carcinomas.
|
21489049 |
2011 |
Undifferentiated carcinoma
|
0.300 |
Biomarker
|
disease |
CTD_human |
Methylation silencing of angiopoietin-like 4 in rat and human mammary carcinomas.
|
21489049 |
2011 |
Carcinomatosis
|
0.300 |
Biomarker
|
phenotype |
CTD_human |
Methylation silencing of angiopoietin-like 4 in rat and human mammary carcinomas.
|
21489049 |
2011 |
Mammary Carcinoma, Animal
|
0.300 |
Biomarker
|
disease |
CTD_human |
Methylation silencing of angiopoietin-like 4 in rat and human mammary carcinomas.
|
21489049 |
2011 |
Solid Neoplasm
|
0.020 |
Biomarker
|
phenotype |
BEFREE |
We have also shown that cross-presentation of PR1 by solid tumors renders them susceptible to killing by PR1-targeting immunotherapies.
|
29661776 |
2018 |
Solid Neoplasm
|
0.020 |
GeneticVariation
|
phenotype |
BEFREE |
In patients with detected hotspot TP53 mutant advanced solid tumors (n = 11), the treatment led to a 45% rate of SD ≥6 months/PR (1 PR and 3 SD ≥6 months), median PFS of 3.5 months, and median OS of 12.7 months, compared favorably with the results for patients with undetected hotspot TP53 mutations (n = 25): 16% (1 PR and 3 SD ≥6 months, P = 0.096), 2.0 months (P = 0.042), and 7.4 months (P = 0.1), respectively.
|
25669829 |
2015 |
Pancreatic carcinoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
The tumoral expression of PRTN3 reinforces the therapeutic potential of PR1-targeting immunotherapy in pancreatic cancer.
|
30880498 |
2019 |
Malignant neoplasm of pancreas
|
0.010 |
Biomarker
|
disease |
BEFREE |
The tumoral expression of PRTN3 reinforces the therapeutic potential of PR1-targeting immunotherapy in pancreatic cancer.
|
30880498 |
2019 |
Malignant tumor of colon
|
0.010 |
Biomarker
|
disease |
BEFREE |
ULBP2 might be a potential novel OS prognostic biomarker in CC, while GRP and TMEM37 could be served as the independent DFS prognostic genes in CC.
|
29653552 |
2018 |
Colon Carcinoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
ULBP2 might be a potential novel OS prognostic biomarker in CC, while GRP and TMEM37 could be served as the independent DFS prognostic genes in CC.
|
29653552 |
2018 |