Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Tumor markers such as carcinoembryonic antigen (CEA) and cancer antigen 15-3 (CA15-3) are widely used for monitoring breast cancer.
|
31312932 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Very recently, the EMA has approved durvalumab for the treatment of patients with unresectable stage III NSCLC not progressing after chemoradiotherapy and whose tumors express PD-L1 on ≥1% of TC.
|
30775032 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Evaluation of two tumour markers (carcinoembryonic antigen and cancer antigen 15-3) showed that there was no significant difference between before and after treatment.
|
30887570 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Expression of Mucin 1 in salivary gland tumors and its correlation with clinicopathological factors.
|
30916513 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
All tested cases displayed concomitant loss of SMARCA4 and SMARCA2 and most tumors expressed epithelial markers (Pan-keratin or EMA) (n=29/30), SOX2 (n=26/27), and CD34 (n=17/27).
|
30451731 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Tumor-associated MUC1 is expressed on over 90 % of all breast cancer entities and differs strongly from its physiological form on epithelial cells, therefore presenting a unique target for breast cancer diagnosis and antibody-mediated immune therapy.
|
31588183 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Herein, a tumor cell specific "switch-on" PDT nanoplatform, which employs a well-designed hairpin structure mucl protein (MUC1) aptamer (Apt) as specific linker to conjugate gold nanorod and Chlorin e6 (Ce6) (GNR/Apt-Ce6) is prepared, and "switch on" via conformational changes of aptamer-induced fluorescence resonance energy transfer missing between GNR and Ce6 for selective tumor therapy.
|
31532896 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
In the present study, we demonstrate that MUC1 downregulates the expression of the tumor suppressor polypeptide N-acetylgalactosaminyltransferase 5 in pancreatic cancer.
|
31283009 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Additionally, image cytometry analysis of scanned tumors indicates that the PDE5 inhibitor Tadalafil in conjunction with the MUC1/polyICLC vaccine effectively reduces the number of PDL1<sup>+</sup>macrophages present at the tumor edge, and increases the number of activated tumor infiltrating T cells, suggesting reversion of immune exclusion.
|
31214178 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
MUC1-C represses the RASSF1A tumor suppressor in human carcinoma cells.
|
31435022 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
No significant decrease was found in serum CA 15-3 and tumor PGE2 levels in simvastatin and tamoxifen treated groups as compared to D1 group.
|
29962034 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
We investigated induction of antigen-specific, cytotoxic T-lymphocytes to the well-defined tumor associated antigens (TAAs) hTERT, MUC1, MAGE-C1 and CS1, which have been shown to be expressed in a high proportion of cases of multiple myeloma.
|
31428094 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
MUC1-C thereby contributes to the integration of PRC2 and PRC1-mediated repression of tumor suppressor genes, such as CDH1, CDKN2A, PTEN and BRCA1.
|
29379165 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Given that immunoassays for CA 15-3 and CA 27.29 target epitopes on the same glycoprotein-Mucin 1 (MUC1)-the present analysis was conducted to evaluate the potential concordance of tumor marker results when both tests were ordered by providers on the same specimens.
|
28929449 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
However, by co-expressing 2G CAR.MUC1 (signal 1 - activation + signal 2 - co-stimulation) and 4/7ICR (signal 3 - cytokine), transgenic T cells selectively expanded at the tumor site and produced potent and durable tumor control in vitro and in vivo.
|
29747685 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Here, we assessed MUC1 expression by immunohistochemistry using tumor samples from patients with biopsy-proven NSCLC.
|
30479696 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
The results showed that co-administration of an adjuvant plasmid and a DNA vaccine stimulated the production of higher titers of specific antibodies and a T cell response and suppressed the growth of subcutaneous tumors expressing MUC1.
|
30111221 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Expression of membrane-bound mucin (MUC1) and secretory mucin (MUC2) in CRC (mRNA, protein) were analyzed in tissue material including fragments of tumors obtained from CRC patients (<i>n</i> = 34), and fragments of normal colorectal tissue from the same patients (control).
|
30271081 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Tumor cell-endothelial adhesion is one of the key steps in tumor cell haematogenous dissemination in metastasis and was previously shown to be mediated by interaction of galectin-3 with the transmembrane mucin protein MUC1.
|
30171204 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Furthermore, the anti-hMUC1 antibody was specifically localized in the MUC1-expressing breast cancer cell-derived tumors in xenograft mouse models.
|
29290794 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Breast cancer patients had significantly higher serum RNA loads (AUC 0.665), lower miR-34a (AUC 0.772), higher CEA and CA 15-3 levels (AUCs 0.717 and 0.721) than healthy controls. miR-34a correlated with tumor stage and hormone receptor status.
|
29854296 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Tumor-associated MUC1 is a promising antigen for the design of antitumor vaccines.
|
29345713 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Moreover, DOX-KLA-anti-MUC1-micelle remarkably inhibited tumor growth of tumor-bearing mice when compared with free drug.
|
29317345 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
These data suggested that the single domain based Muc1-Bi may provide a valid strategy for targeting tumors with Muc1 overexpression.
|
29357376 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Here, we constructed a MUC1 and survivin (MS) combination gene tumor vaccine expressing MS fused with soluble PD-1 (sPD1/MS).
|
29894719 |
2018 |