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Links from GEO DataSets

Items: 20

1.

Expression data of GFP-high or low cells of LGR5-GFP or KRT20-GFP knock-in human colorectal tumor organoids.

(Submitter supplied) We analyzed gene expression of 3 lines LGR5-GFP, 2 lines KRT20-GFP knock-in colorectal tumor organdies. The cancer stem cell (CSC) theory highlights a self-renewing subpopulation of cancer cells that fuels tumour growth. The existence of human CSCs is mainly supported by xenotransplantation of prospectively isolated cells, but their clonal dynamics and plasticity remain unclear. Here, we show that human LGR5+ colorectal cancer cells serve as CSCs in growing cancer tissues. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL15207
14 Samples
Download data: CEL
Series
Accession:
GSE83513
ID:
200083513
2.

The role of Lgr5 intestinal cancer stem cells in tumour initiation, progression and metastasis

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Genome variation profiling by high throughput sequencing; Other
Platform:
GPL17021
48 Samples
Download data: TSV, TXT, VCF
Series
Accession:
GSE92966
ID:
200092966
3.

Whole exome sequencing of murine derived intestinal tumour organoids [exome-capture]

(Submitter supplied) DNA was isolated from Apcmin/+;KrasLSL-G12D/+;VillinCre;Lgr5DTReGFP (AKVL), Apcmin/+;KrasLSL-G12D/+;VillinCre;Lgr5DTReGFP;p53KO (AKVPL) and Apcmin/+;KrasLSL-G12D/+;VillinCre;Lgr5DTReGFP;p53KO,Smad4KO (AKVPSL) organoids as well as the spleen of the AKVL donor animal The "SAMPLE_ID" sample characteristic is a sample identifier internal to Genentech.
Organism:
Mus musculus
Type:
Other
Platform:
GPL17021
4 Samples
Download data: VCF
Series
Accession:
GSE92952
ID:
200092952
4.

Whole genome sequencing of murine derived intestinal tumour organoids

(Submitter supplied) DNA was isolated from Apcmin/+;KrasLSL-G12D/+;VillinCre;Lgr5DTReGFP (AKVL), Apcmin/+;KrasLSL-G12D/+;VillinCre;Lgr5DTReGFP;p53KO (AKVPL) and Apcmin/+;KrasLSL-G12D/+;VillinCre;Lgr5DTReGFP;p53KO,Smad4KO (AKVPSL) organoids as well as the spleen of the AKVL donor animal The "SAMPLE_ID" sample characteristic is a sample identifier internal to Genentech.
Organism:
Mus musculus
Type:
Genome variation profiling by high throughput sequencing
Platform:
GPL17021
4 Samples
Download data: TXT
Series
Accession:
GSE92950
ID:
200092950
5.

Profiling of AKVPL derived tumors after depletion of Lgr5+ cells

(Submitter supplied) RNA was isolated from fluorescence activated cell sorted (FACS) CD45 negative, EpCAM positive bulk tumor cells from Apcmin/+;KrasLSL-G12D/+;VillinCre; Lgr5DTReGFP;p53KO (AKVPL) intestinal tumours at different time points after a single dose of vehicle saline or diphteria toxin. The "SAMPLE_ID" sample characteristic is a sample identifier internal to Genentech. The ID of this project in Genentech's ExpressionPlot database is PRJ0011163
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
24 Samples
Download data: TSV
Series
Accession:
GSE92949
ID:
200092949
6.

Profiling of AKVPL vs AKVPSL derived tumor cells (Mouse)

(Submitter supplied) RNA was isolated from fluorescence activated cell sorted (FACS) Lgr5-GFP+ and Lgr5-GFP- from aged matched subcutaneously implanted Apcmin/+;KrasLSL-G12D/+;VillinCre; Lgr5DTReGFP;p53KO (AKVPL) and Apcmin/+;KrasLSL-G12D/+;VillinCre; Lgr5DTReGFP;p53KO;SMAD4KO (AKVPSL) intestinal tumours. "SAMPLE_ID" sample characteristic is a sample identifier internal to Genentech. The ID of this project in Genentech's ExpressionPlot database is PRJ0009421
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
16 Samples
Download data: TSV
Series
Accession:
GSE84812
ID:
200084812
7.

Lgr5-Expressing Chief Cells Drive Epithelial Regeneration and Cancer in the Oxyntic Stomach

(Submitter supplied) Adult stem cells residing within tubular glands of the corpus epithelium are believed to fuel daily tissue renewal, but their identity remains controversial. Lgr5, marks both homeostatic stem cells and “reserve” stem cells in multiple tissues. Here, we report Lgr5 expression in a subpopulation of chief cells in mouse and human corpus glands. Using a new, non-variegated Lgr5-2A-CreERT2 mouse model, we show by cell fate mapping that Lgr5-expressing chief cells do not behave as corpus stem cells under homeostatic conditions, but are recruited to function as stem cells to effect epithelial renewal following injury. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL16570
21 Samples
Download data: CEL
Series
Accession:
GSE86603
ID:
200086603
8.

Whole-genome transcriptomic analysis of Notch1-expressing cells in mouse intestinal tumours

(Submitter supplied) To define and compare the genome-wide transcriptional signatures of Notch1+ cells in intestinal tumors and in normal ISCs we performed Affymetrix analyses of these two populations.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL24707
12 Samples
Download data: CEL
Series
Accession:
GSE111594
ID:
200111594
9.

3' droplet-based single cell RNA sequencing of a mouse large intestinal epitherlium

(Submitter supplied) Using 3' droplet-based single-cell sequencing, we performed the transcriptional profiling of mouse large intestinal epithelial cells at the single-cell level.
Organism:
Mus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL31136
1 Sample
Download data: MTX, TSV
Series
Accession:
GSE209649
ID:
200209649
10.

FGF Signaling in the Self-Renewal of Colon Cancer Organoids

(Submitter supplied) With their ability to self-renew and simultaneously fuel the bulk tumor mass with highly proliferative tumor cells, cancer stem cells (CSC) are supposedly driving cancer progression. However, the CSC-phenotype in colorectal cancer (CRC) is unstable and dependent on environmental cues. Since FGF2 is essential for adult and embryonic stem cell culture to maintain self-renewal, we investigated its role in advanced CRC using tumor-derived organoids as experimental model. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL16043
9 Samples
Download data: CEL
Series
Accession:
GSE118949
ID:
200118949
11.

Gene expression changes with LGR5 knockdown in LoVo colon cancer cells

(Submitter supplied) The goal of this study was to identify gene expression changes in response to loss of LGR5 in the LoVo colon cancer cell line.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
6 Samples
Download data: TXT
Series
Accession:
GSE135749
ID:
200135749
12.

In vitro expansion of single adult Lgr5+ liver cells induced by Wnt-driven regeneration

(Submitter supplied) The Wnt target gene Lgr5 marks actively dividing stem cells in Wnt-driven, self-renewing tissues such as small intestine and colon, stomach and hair follicles. A 3D culture system allows long-term clonal expansion of single Lgr5+ stem cells into transplantable organoids that retain many characteristics of the original epithelial architecture. A crucial component of the culture medium is the Wnt agonist Rspo, the recently discovered ligand of Lgr5. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL4134
28 Samples
Download data: TXT
Series
Accession:
GSE32210
ID:
200032210
13.

PROX1 mediates chemoresistance-associated recurrence via maintenance of quiescent colon cancer stem cells

(Submitter supplied) Cancer stem cells (CSCs) are profoundly associated with refractory nature of cancer. A quiescent population of CSCs is responsible for tumorigenesis and chemoresistance in leukemia, whereas neither the presence nor clinical importance of the quiescent CSCs is clearly established in solid tumors. In colon cancer, LGR5 is regarded as a functional marker of CSCs, but heterogeneity among LGR5+ cells was not clearly defined. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
56 Samples
Download data: CSV
Series
Accession:
GSE141157
ID:
200141157
14.

LGR5 marks targetable tumor-initiating cells in liver cancer

(Submitter supplied) We want to investige the difference betwen untreated/5-FU treated LGR5+/LGR5- cell population, by adopting RNA-sequencing.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
12 Samples
Download data: XLS
Series
Accession:
GSE137517
ID:
200137517
15.

Stem cell functionality is microenvironmentally defined during tumor expansion and therapy response in colon cancer

(Submitter supplied) Solid malignancies have been speculated to depend on cancer stem cells (CSCs) for expansion and relapse after therapy. Here we report on quantitative analyses of lineage tracing data from primary colon cancer xenograft tissue to assess CSC functionality in a human solid malignancy. The temporally obtained clone size distribution data support a model in which stem cell function in established cancers is not intrinsically but entirely spatiotemporally orchestrated. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
12 Samples
Download data: CSV
16.

Expression profiling of Lgr5 positive adenoma cells.

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL4134
12 Samples
Download data: TXT
Series
Accession:
GSE37929
ID:
200037929
17.

Comparison of gene expression patterns between Lgr5 positive cells in adenomas and small intestine

(Submitter supplied) The generation of the Lgr5_EGFP_ires_CreERT2 knock-in mouse allows marking of Lgr5 positive cells of different tissues by GFP expression. Here we use these mice to sort GFP positive cells from intestinal adenomas and compare those to GFP positive cells from normal small intestine.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL4134
6 Samples
Download data: TXT
Series
Accession:
GSE37928
ID:
200037928
18.

Gene expression profiling of Lgr5 positive cells within intestinal adenomas

(Submitter supplied) The generation of the Lgr5_EGFP_ires_CreERT2 knock-in mouse allows marking of Lgr5 positive cells of different tissues. Here we use these mice to sort Lgr5 positive cells and their daughter cells form intestinal adenomas and describe the expression profile of these two cell populations.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL4134
6 Samples
Download data: TXT
Series
Accession:
GSE37926
ID:
200037926
19.

COMPARATIVE TRANSCRIPTOMIC AND PROTEOMIC ANALYSIS OF LGR5+ve STEM CELLS AND THEIR DAUGHTERS

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array
Platforms:
GPL11180 GPL4134
10 Samples
Download data: CEL, TXT
Series
Accession:
GSE33949
ID:
200033949
20.

COMPARATIVE TRANSCRIPTOMIC AND PROTEOMIC ANALYSIS OF LGR5+ve STEM CELLS AND THEIR DAUGHTERS (AFFYMETRIX ARRAYS)

(Submitter supplied) The identification of Lgr5 as an intestinal stem cell marker has made it possible to isolate and study primary intestinal stem cells. Applying quantitative mass spectrometry as well as transcriptomic analysis, we profiled the protein and gene changes between FACS-sorted Lgr5+ve stem cells and their immediate undifferentiated daughter cells. The overall comparison of mRNA and protein levels revealed a high level of correlation, implying that the initial control of intestinal stem cell biology occurs largely at the mRNA level. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL11180
6 Samples
Download data: CEL
Series
Accession:
GSE33948
ID:
200033948
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