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Links from GEO DataSets

Items: 13

1.
Full record GDS2454

Tumor-induced CD11b+ splenocyte

Analysis of CD11b+ splenocytes from tumor-bearing animals. Tumor development often leads to the accumulation of CD11b+ GR-1 myeloid cells. Results provide insight into the molecular basis of the immunosuppressive activity exhibited by tumor-induced CD11b+ splenocytes.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 disease state, 2 growth protocol sets
Platform:
GPL81
Series:
GSE5455
9 Samples
Download data
2.

Gene expression profiling of CD11b purified from mouse spleen (tumor-free and tumor-bearing mice)

(Submitter supplied) Active suppression of tumor-specific T lymphocytes can limit the immune-surveillance and immunotherapy efficacy. While tumor-recruited CD11b+ myeloid cells are known mediators of tumor-associated immune dysfunction, the true nature of these suppressive cells and the fine biochemical pathways governing their immunosuppressive activity remain elusive. Here we describe a population of circulating CD11b+/IL-4Rα+, inflammatory-type monocytes that is elicited by growing tumors and activated by IFN-γ released from T lymphocytes. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS2454
Platform:
GPL81
9 Samples
Download data
Series
Accession:
GSE5455
ID:
200005455
3.

Pten null prostate epithelium promotes localized myeloid-derived suppressor cell expansion and immune suppression during tumor initiation and progression

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL10361
21 Samples
Download data: TXT
Series
Accession:
GSE56470
ID:
200056470
4.

Pten null prostate epithelium promotes localized myeloid-derived suppressor cell expansion and immune suppression during tumor initiation and progression [microdissected tissue]

(Submitter supplied) Chronic inflammation is known to associate with prostate cancer development, but how epithelium-associated cancer initiating events cross-talk to inflammatory cells during prostate cancer initiation and progression is largely unknown. Using the Pten null murine prostate cancer model, we show an expansion of Gr-1+CD11b+ myeloid-derived suppressor cells (MDSCs) occurring intra-prostatically immediately following epithelium-specific Pten deletion without expansion in hematopoietic tissues. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL10361
6 Samples
Download data: TXT
Series
Accession:
GSE56469
ID:
200056469
5.

Pten null prostate epithelium promotes localized myeloid-derived suppressor cell expansion and immune suppression during tumor initiation and progression [cell lines]

(Submitter supplied) Chronic inflammation is known to associate with prostate cancer development, but how epithelium-associated cancer initiating events cross-talk to inflammatory cells during prostate cancer initiation and progression is largely unknown. Using the Pten null murine prostate cancer model, we show an expansion of Gr-1+CD11b+ myeloid-derived suppressor cells (MDSCs) occurring intra-prostatically immediately following epithelium-specific Pten deletion without expansion in hematopoietic tissues. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL10361
15 Samples
Download data: TXT
Series
Accession:
GSE56468
ID:
200056468
6.

Nanostring analysis of MC38 tumors in PBS and hetIL-15-treated mice

(Submitter supplied) Comparison of gene expression identified several significantly overexpressed genes in tumors recovered from hetIL-15-treated mice. These upregulated genes after hetIL-15 treatment represent an expression signature that corresponds to activated TILs with cytotoxic phenotype. Nanostring analysis also identified additional functional pathway signatures, including signal transducer and activator of transcription (STAT) intracellular signaling, TCR recognition of cognate antigen, interferons signaling, increased metabolic rate and immune cell chemotaxis
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL28519
11 Samples
Download data: RCC, XLSX
Series
Accession:
GSE150357
ID:
200150357
7.

RNA Sequencing of Intratumoral Immune Populations in Pancreatic Ductal Adenocarcinoma Following Radiotherapy and Interleukin 12 Treatment

(Submitter supplied) We report differential gene expression in inflammatory monocyte (IM), tumor-associated macrophage (TAM), and CD8 T cell populations following stereotactic body radiation (SBRT), intratumoral interleukin 12 microsphere (IL-12 MS) delivery, and SBRT/IL-12 MS combination. Immune cell populations were sorted from orthotopic murine pancreatic ductal adenocarcinoma (PDA) tumors prior to RNA sequencing.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
33 Samples
Download data: TXT
Series
Accession:
GSE136368
ID:
200136368
8.

Myeloid cell-based delivery of IFN-γ reprograms leukemia microenvironment and induces anti-tumoral immune responses

(Submitter supplied) The immunosuppressive microenvironment surrounding tumor cells represents a key cause of treatment failure. Therefore, immunotherapies aimed at reprogramming the immune system have largely spread in the past years. We employed gene transfer into hematopoietic stem and progenitor cells to selectively express anti-tumoral cytokines in tumor-infiltrating monocytes/macrophages. We show that Interferon-γ (IFNγ) reduced tumor progression in mouse models of B-cell acute lymphoblastic leukemia (B-ALL) and colorectal carcinoma (MC38). more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL24247
11 Samples
Download data: CSV, MTX, TSV
Series
Accession:
GSE178941
ID:
200178941
9.

Gene expression profiling of CD45+CD11b+F4/80high macrophages in MC38 tumor of WT mice injected with DMSO or picrotoxin

(Submitter supplied) We characterized tumor-associated macrophages and found a pro-inflammatory signature of those cells in picrotoxin-treated mice compared to those in control mice (DMSO).
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16417
12 Samples
Download data: TXT
Series
Accession:
GSE183246
ID:
200183246
10.

Gene expression profiling of CD45+CD11b+F4/80high macrophages and CD45+TCRbeta+CD8+ T cells in MC38 tumor of WT, muMt-/- or muMt-/- mice implanted with GABA pellet

(Submitter supplied) We characterized the tumor-infiltrating macrophages and CD8 T cells, and we found a pro-inflammatory signature of those cells in muMt-/- mice compared to those in WT mice. Furthermore, many target genes of inflammatory cytokines, such as the TNF target genes, highly expressed in muMt-/- mice, were downregulated by exogenous of GABA.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16417
36 Samples
Download data: TXT
Series
Accession:
GSE169543
ID:
200169543
11.

Single cell RNA sequencing of the lung pre-metastatic niche in a syngeneic mouse model of rhabdomyosarcoma

(Submitter supplied) C57BL/6 mice were injected orthotopically with M3-9-M ffluc-mCherry rhabdomyosarcoma tumor cells in the gastrocnemius muscle of the leg. Mice were treated with 8E6 IL12-secreting genetically engineered myeloid cells (IL12-GEMys) on day 12 post tumor inoculation. Lungs were harvested 3 days post IL12-GEMy treatment, 15 days post primary tumor inoculation. 3' single cell RNA-Seq was performed on isolated cells.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
14 Samples
Download data: H5
Series
Accession:
GSE168297
ID:
200168297
12.

RNA sequencing of the lung pre-metastatic niche in a syngeneic mouse model of rhabdomyosarcoma

(Submitter supplied) The objective of this study was to profile the transcriptional landscape in the pre-metastatic lungs of mice with and without IL12-GEMy treatment.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
17 Samples
Download data: TXT
Series
Accession:
GSE166763
ID:
200166763
13.

Tumor-infiltrating CCR2+ inflammatory monocytes counteract specific immunotherapy

(Submitter supplied) We used Single-cell RNA-sequencing to analyze the composition of the tumor microenvironment of MC38mOVA tumors upon transcutaneous immunization with our immunization method DIVA.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
2 Samples
Download data: CSV
Series
Accession:
GSE239384
ID:
200239384
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