Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Sphere-forming cells dissociated from tumorspheres heterogeneously expressed CD44, CD54, and epithelial cell adhesion molecule (EpCAM) markers and generated one tumor in nude mice.
|
30641083 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
To elucidate the role of ICAM-1 on the crosstalk between tumor and primary liver sinusoidal endothelial cells (LSECs) and hepatic stellate cells (HSCs), implicated in tumor adhesion and angiogenesis, we performed in vitro cocultures and an in vivo model of liver metastasis of colorectal cancer (CRC).
|
31511625 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
The I/R-induced renal inflammation was evaluated by determining leukocyte infiltration and mRNA expression level of intercellular adhesion molecule-1 and tumor necrotic factor-alpha (TNF-α).
|
31249267 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Clinical responses were correlated with PD-L1 expression on tumor cells, the presence of tumor infiltrating lymphocytes (TIL), baseline tumor volume, ECOG performance status, serum LDH levels, high percentage of activated CD8+ T cells and CD3- CD16+ CD54+ NK cells in the peripheral blood as well as tumor mutational burden (TMB).
|
30642373 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Furthermore, strong induction of ICAM-1 in tumor vessels was associated with significantly augmented trafficking of adoptively transferred <i>in vitro</i>-activated CD8<sup>+</sup> T cells to tumors after RFA.
|
31795828 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
It has been reported that soluble ICAM-1 allows tumor cells to escape from immune recognition and stimulates angiogenesis and tumor growth.
|
31205504 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
TNFα supplementation in dysbiotic mice was able to increase ICAM-1 expression and leukocyte trafficking into the tumor.
|
31591154 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Higher ICAM1 and ULBP1 tumor expression correlated with improved patient survival in two non-small cell lung cancer (NSCLC) cohorts.
|
31488404 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Focusing on the tumour suppressor miRNA, bta-miR-181a and bta-miR-181b, we identified putative messenger RNA targets and confirmed the interaction of bta-miR181a with ICAM-1.
|
30370674 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Since ICAM-1, which can promote tumor cell/T-cell interaction and T-cell activation, is highly expressed on EWS-FLI1 low cells, we hypothesized that EWS-FLI1 low cells would be more susceptible to T-cell mediated tumor cell apoptosis as compared to cells with high EWS-FLI1.
|
31164960 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
We found that (1) manual and automatic quantification of tumor-infiltrating immune cells were consistent; (2) RME tumors showed a higher degree of immune cell infiltration than RMA tumors but (3) the number of tumor infiltrating lymphocytes was low compared to other solid tumor types; (4) microvascular density correlated with immune cell infiltration and (5) CD163 positive macrophages as well as CD54 positive microvessels were more often detected in RME than in RMA and correlated with patient overall and event free survival.
|
31239476 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
ICAM-1 also demonstrated a significant decrease in stage III/IV compared with stage I/II tumors.
|
31308754 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
The expression level of ICAM-1 in papillary thyroid carcinoma was also significantly higher than that in other types of tumors.
|
30119270 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
We propose that ICAM-1-mediated homotypic T-lymphocyte aggregation may serve as a tumor-mediated immune retention mechanism entrapping activated CD8+ T cells in the tumor microenvironment.
|
30258446 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Tumor growth rate and final tumor weight were significantly increased in the animals with the glioblastoma derived from transfected U87-H4645 cells, compared to untransfected and vector control (p<0.01). mRNA expression of β-catenin, CD44, ICAM-1, and MMP-2 in the glioblastoma derived from the transfected U87-H4645 tumors was significantly increased compared with tumors derived from untransfected and vector-control U87 cells (p<0.01).
|
29848673 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
For the first time, we provide proof-of-principle evidence that in vitro TNBC cell-ICAM1 antibody binding force measured by AFM on live cells more precisely correlates with in vivo tumor accumulation and therapeutic efficacy of ICAM1 antibody-directed liposomes than ICAM1 gene and surface protein overexpression levels.
|
29505261 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
MicroSPECT imaging of triple negative breast cancer cell tumor xenografted in athymic mice with radioiodinated anti-ICAM-1 monoclonal antibody.
|
29684714 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
There was a weak correlation between tumor size and serum level of ICAM1 with Pearson score correlation, but there was no significant correlation with VEGF.
|
28643744 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
The endothelial cells of tumor central were damaged, but the lumen area of the tumor peripheral vessels (TPVs) and the expression of ICAM‑1 on HUVECs were increased after SDT.
|
30106435 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Finally, we showed a clinical correlation between CX3CL1 expression and ICAM-1 expression as well as tumor stage in human osteosarcoma tissues.
|
28903329 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Patient-derived ATC cells overexpressed ICAM-1 and were largely eliminated by autologous ICAM-1 CAR T cells <i>in vitro</i> and in animal models.<b>Conclusions:</b> Our findings are the first demonstration of CAR T therapy against both a metastatic, thyroid cancer cell line and advanced ATC patient-derived tumors that exhibit dramatic therapeutic efficacy and survival benefit in animal studies.<i></i>.
|
29025766 |
2017 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
However, immunohistochemistry staining of progression tissue microarray comprised of samples of different disease stages derived from different patients, demonstrated a dramatic ICAM-1 upregulation particularly upon the transition from primary tumor to lymph node metastasis.
|
29245925 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Our findings suggest that ICAM-1 is a potentially important mediator of tumor migration and invasion in bevacizumab-resistant glioblastoma.
|
29228586 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
We further evaluated ICAM-1 as a MM targeting moiety by characterizing its (1) tumor specificity, (2) expression level, (3) cellular internalization, (4) therapeutic function, and (5) potential clinical impact.
|
28341549 |
2017 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
ICAM-1 upregulation resulted in increased conjugate formation between the NK cells and tumor cells, which can contribute to the increased sensitivity observed.
|
28428785 |
2017 |