Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
Tumors with MSI-H were associated with the following: dense infiltration (CD45, P < 0.001); cytotoxic CD8-positive lymphocytes (P < 0.001); and a complete absence of HLA class I cell surface expression, due to inactivating β2-microglobulin (β2-m) mutation in 50% of cases.
|
21400022 |
2011 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Tumor OGN expression levels were positively associated with CD3, CD8, and PTPRC expressions in the training and testing sets from TCGA, respectively.
|
30037719 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
A diagnosis of HS was made based on the results of a panel of immunohistochemical stains that revealed positivity of leukocyte common antigen, CD4, CD163, and HLA-DR. At the time of resection, the tumor grew rapidly to 12 × 6.5 × 5 cm in size in 2 months.
|
31567137 |
2020 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
A single dose of rituximab during the primary tumor heterotransplantation process reduced the incidence of CD45-positive cells in subsequent PDX lines from 86.3% (n = 117 without rituximab) to 5.6% (n = 160 with rituximab), and the lymphoma rate declined from 11.1% to 1.88%.
|
28658648 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Abundant B220+ B lymphocyte infiltrates with interspersed CD138+ plasma cells were recruited to the MDR1A KO tumor microenvironment, concomitant with high levels of immunoglobulin light chain genes.
|
28686677 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
After CIK treatment, the tumor tissue nodules formed and a large amount of lymphocytes infiltrated in the liver cancer tissue and CD3, CD45, CD45RO, and CD68 increased greatly which was shown by immunohistochemistry.
|
15948236 |
2005 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
After the treatment period, the tumor tissues were weighed and harvested for mRNA and protein isolation. qPCR and Western blotting were used to evaluate the expression of cancer stemness markers (epithelial cell adhesion molecule [EpCAM], cluster of differentiation [CD13], CD90, aldehyde dehydrogenase 1 [ALDH1], CD44, and CD45), totipotency factors (sex determining region Y-box 2 [Sox2], Nanog, and octamer-binding transcription factor 4 [Oct4]), and genes involved in the Notch, Wnt/<i>β</i>-catenin, Hedgehog, and Hippo signaling pathways.
|
31341493 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
By immunophenotyping, these neoplasms expressed leukocyte common antigen and HLA-DR but did not show consistent immunostaining for B-cell or T-cell differentiation antigens.
|
1880251 |
1991 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Cells with the phenotype of tumor plasma cells (CD38(++)CD19(-)CD45(-/+)CD56(-/+/++)) or memory B cells (CD38(-)/CD19(+)/CD27(+)) were isolated by flow activated cell sorting.
|
20511669 |
2010 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Collectively, our data suggest that the Gal-1 aptamer suppresses tumor growth by blocking the interaction between Gal-1 and CD45 to rescue T cells from apoptosis and restores T cell-mediated immunity.
|
31778957 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Despite heterogeneous dynamics of clinical tumor regression, residual tumors displayed highly recurrent transcriptomic alterations and enriched processes, which were also observed in MAPKi-selected cell lines (implying tumor cell-intrinsic reprogramming) or in bulk mouse tumors (and the CD45-negative or CD45-positive fractions, implying tumor cell-intrinsic or stromal/immune alterations, respectively).
|
28864476 |
2017 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Different B-cell neoplasias vary in the expression of CD45 isoforms.
|
11378582 |
2001 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Ex vivo treatment of primary myeloma cells with 17DMAG resulted in a stronger caspase3 activation in tumor samples with the prevalence of high CD45 expressers.
|
23246572 |
2013 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Exact determination of tumor cell DNA content was done by referring to the CD45-positive tissue leukocyte fraction as the internal diploid reference cell population.
|
12210600 |
2002 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Finally, restoring IFI16 protein to HNO136 cells increased CD45+ inflammatory cell infiltration of the tumor burden, predominantly consisting of CD68/CD14 positive macrophages.
|
19553003 |
2010 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Formalin-fixed, paraffin-embedded breast cancer samples were analysed on tissue microarrays using mIF, which combined phospho-histone H3 (pHH3) expression with cytokeratin (CK) and leukocyte common antigen (CD45) expression to identify tumour and immune cells, respectively.
|
31410680 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Furthermore, LTD4 or PGE2 accentuated the accumulation of CD45 expressing cells within xenograft tumors.
|
27388564 |
2016 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Furthermore, the cell lines expressing syndecan were negative for CD19 and CD45 staining, indicating that syndecan expression is restricted to tumors having a well-differentiated phenotype.
|
8427968 |
1993 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Here, we demonstrated that the <i>in vivo</i> injection of recombinant human IL-15 (200 µg/kg) or murine IL-15 (3 µg/kg) to tumor-bearing NOD-<i>SCID-IL2Rg-/-</i> (NSI) mice resulted in increased tumor progression and CD45+ CD11b+ Gr-1+ CD215+ cell expansion in the tumors and spleen.
|
29255466 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Histopathological diagnosis of the tumor was a high-grade lymphoma of the diffuse type containing cells positive for B cell specific antigen (CD20) and negative for the leukocyte common antigen (CD45).
|
11734324 |
2001 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Immunohistochemical analysis revealed that CD45R/B220+ and Gr-1+ cells had infiltrated into the tumor tissue of the SW1990/si-MUC5AC cells.
|
21249315 |
2011 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Immunohistochemical staining established the T-cell origin of the neoplasm with strong expression of CD45, CD3, CD43, and CD2 and also showed expression of CD30 consistent with the histologic features that suggested ALCL.
|
15104308 |
2004 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Immunologic data of PCNA-positive cell ratios and CD45-positive cell ratios of the tumor specimens in the three groups were as follows: 1) control group: 65.72% (PCNA) and 0.92% (CD45), 2) NK treatment group: 27.66% (PCNA) and 13.46% (CD45), and 3) PD-1 inhibited NK cells treatment group: 13.66% (PCNA) and 23.66% (CD45) (P<0.001).
|
26266810 |
2015 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Immunophenotyping of the tumour using immunohistochemistry and flow cytometry revealed LCA+, CD4+, CD56+, CD43+, TdT+, CD2-, cCD3-, CD8-, CD7-, CD34- and TIA-1-.
|
9870150 |
1998 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In a previous work, we showed that in TNBC miR-210 is expressed in tumor cells and also in the tumor microenvironment (TME), particularly in inflammatory CD45-LCA positive cells.
|
31787032 |
2020 |