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Links from GEO DataSets

Items: 20

1.

MicroRNA expression data from high and low invasive A549 human lung adenocarcinoma cells

(Submitter supplied) The major cause of cancer-related deaths in lung cancer patients is commonly attributed to its ability to metastasize to distant organs such as the bone, brain, liver and adrenal glands. The dysregulation in miRNA expression is believed to contribute toward the initiation and progression of metastasis through their capability to regulate target genes. In this study, two NSCLC sub-cell lines possessing opposing migration and invasion properties were established using serial transwell invasion assays, followed by miRNA microarray to obtain the overview of miRNA expression as well as identify important playes in metastasis.
Organism:
synthetic construct; Homo sapiens
Type:
Non-coding RNA profiling by array
Platform:
GPL8786
6 Samples
Download data: CEL
Series
Accession:
GSE47056
ID:
200047056
2.

MicroRNA expression data from Bcl-xL silenced A549 lung adenocarcinoma cells

(Submitter supplied) Bcl-xL is an anti-apoptotic protein that is frequently found to be overexpressed in non-small cell lung cancer leading to an inhibition of apoptosis and poor prognosis. Recently, the role of miRNAs in regulating apoptosis and cell survival during tumorigenesis has become evident, with cancer cells showing perturbed expression of various miRNAs. We utilized miRNA microarrays to determine if miRNA dysregulation in bcl-xL silenced lung adenocarcinoma cells could be involved in regulating apoptotic behavior, and identified dysregulated miRNAs with putative targets involved in signal transduction pathways regulating apoptosis, cell proliferation and cell progression.
Organism:
synthetic construct; Homo sapiens
Type:
Non-coding RNA profiling by array
Platform:
GPL8786
6 Samples
Download data: CEL
Series
Accession:
GSE47059
ID:
200047059
3.

Claudin-1 is an Invasion and Metastasis Suppressor of Lung Adenocarcinoma

(Submitter supplied) Background: Claudin-1(CLDN1), one of the key components of tight junction proteins, was found to be down-regulated in human lung adenocarcinomas. This study we investigated the clinical significance of CLDN1 expression in lung adenocarcinoma patients and its role in cancer progression. Method: CLDN1 mRNA expression was measured in tumor specimens from 51 patients with lung adenocarcinoma. CLDN1 protein expression was also examined by immunohistochemistry on specimens from an independent cohort of 67 lung adenocarcinoma patients. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS3510
Platform:
GPL570
4 Samples
Download data: CEL
Series
Accession:
GSE10309
ID:
200010309
4.
Full record GDS3510

Claudin-1 overexpression effect on lung adenocarcinoma cell line

Analysis of lung adenocarcinoma CL1-5 cells overexpressing Claudin-1 (CLDN1), a component of tight junction complexes. Low CLDN1 expression in lung adenocarcinomas is associated with shorter overall survival. Results provide insight into the role of CLDN1 in the progression of lung adenocarcinoma.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 2 protocol sets
Platform:
GPL570
Series:
GSE10309
4 Samples
Download data: CEL
DataSet
Accession:
GDS3510
ID:
3510
5.

Identification of oral carcinoma miRNA involved in Wnt/b-catenin signaling

(Submitter supplied) MicroRNAs (miRNAs) participate in many biological processes and have emerged as key players in carcinogenesis. In order to identify changes in miRNAs specific for betelquid-associated oral squamous cell carcinoma (OSCC), we investigated the expression profiles of 858 miRNAs in a panel of 40 pairs of OSCC specimens and their matched non-tumorous epithelial counterparts. Eighty-four miRNAs were differentially expressed in the OSCC specimens compared to the matched tissue. more...
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by array
Platform:
GPL8179
80 Samples
Download data: TXT
Series
Accession:
GSE45238
ID:
200045238
6.

A microRNA regulon that mediates endothelial recruitment by metastatic human breast cancer cells.

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platforms:
GPL6947 GPL570
8 Samples
Download data
Series
Accession:
GSE23921
ID:
200023921
7.

miR-126 over-expression in highly metastatic LM2 breast cancer cells.

(Submitter supplied) miR-126 were over-expressed using the miR-Vec system in highly metastatic LM2 cells. The LM2 cell line are described in detail in Minn et al. Nature 2005 This approach was used to conduct an unbiased search for specific miR-126 target genes in breast cancer cells.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platforms:
GPL6947 GPL570
8 Samples
Download data
Series
Accession:
GSE23905
ID:
200023905
8.

Gene expression profilling of poorly metastatic MDA cells and highly metastatic LM2 cells.

(Submitter supplied) Comparison of gene expression between the breast cancer cell line MDA-MB-231 and its highly metastatic deriviate LM2 cells (described in Minn et al., Nature 2005). Results hilghlights potential metastasis promoting and suppressing genes.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6947
4 Samples
Download data: TXT
Series
Accession:
GSE23904
ID:
200023904
9.

PARVA promotes invasion through inducing phosphorylation of ILK signaling in lung cancer

(Submitter supplied) Alpha-parvin (PARVA) is known to involve in the linkage of integrins, regulation of actin cytoskeleton dynamics, and cell survival. However, the role of PARVA in cancer progress is still unclear. Here, we identify PARVA as a potential oncogene from a lung cancer invasion cell line model by expression microarrays. Overexpression of PARVA enhances cell invasion, colony formation ability, and endothelial cell tube formation but knockdown of PARVA inhibits invasion and tube formation in vitro. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
4 Samples
Download data: CEL
Series
Accession:
GSE50657
ID:
200050657
10.

Analysis of gene expression with the Hmga2 allelic series.

(Submitter supplied) In this study, we introduced a series of expression constructs into a mouse lung cancer cell line (482N1): (1) a control short hairpin RNA (shluc) plus the empty expression vector (empty); (2) an shRNA targeting Hmga2 (shHmga2) plus empty; (3) shHmga2 plus an expression vector for the full-length Hmga2 cDNA with the shRNA site mutated (shHmga2 wt); (4) shHmga2 plus the full-length shRNA-mutated Hmga2 with let-7 sites in the 3' UTR mutated (shHmga2 m7); (5) shHmga2 plus the full-length shRNA-mutated Hmga2 with the start codon mutated (shHmga2 ATG wt); and (6) shHmga2 plus the full-length shRNA-mutated Hmga2 with the start codon and let-7 sites mutated (shHmga2 ATG m7).
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
18 Samples
Download data: TXT
Series
Accession:
GSE50932
ID:
200050932
11.

Field of Cancerization in Peripheral Airway Epithelium

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array; Expression profiling by RT-PCR
Platforms:
GPL17039 GPL570
60 Samples
Download data: CEL
Series
Accession:
GSE54543
ID:
200054543
12.

Field of Cancerization in Peripheral Airway Epithelium: miRNA

(Submitter supplied) Field of cancerization in the airway epithelium has been increasing examined to understand early pathogenesis of non-small cell lung cancer. This study uses microarray high-throughput technologies to characterize the molecular aberrations in the terminal airway and bronchoalveolar cells in the context of field cancerization in high-risk smokers and lung cancer patients.
Organism:
Homo sapiens
Type:
Expression profiling by RT-PCR
Platform:
GPL17039
30 Samples
Download data: TXT
Series
Accession:
GSE54541
ID:
200054541
13.

Field of Cancerization in Peripheral Airway Epithelium: Gene Expresssion

(Submitter supplied) Field of cancerization in the airway epithelium has been increasing examined to understand early pathogenesis of non-small cell lung cancer. This study uses microarray high-throughput technologies to characterize the molecular aberrations in the terminal airway and bronchoalveolar cells in the context of field cancerization in high-risk smokers and lung cancer patients.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
30 Samples
Download data: CEL
Series
Accession:
GSE54495
ID:
200054495
14.

Cerebrospinal fluid microRNA profile in leptomeningeal metastasis patients

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by array
Platform:
GPL25134
32 Samples
Download data: TXT
Series
Accession:
GSE125193
ID:
200125193
15.

Cerebrospinal fluid microRNA profile in leptomeningeal metastasis patients [pre- vs post-treatment]

(Submitter supplied) This study aimed to identify specific CSF miRNAs for diagnosing and monitoring leptomeningeal metastasis with lung adenocarcinoma. In discovery phase, we performed miRNA microarray analysis in matched CSF samples from leptomeningeal metastasis patients at diagnosis and after initial leptomeningeal metastasis-directed therapy.
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by array
Platform:
GPL25134
12 Samples
Download data: TXT, XLS
Series
Accession:
GSE125192
ID:
200125192
16.

Cerebrospinal fluid microRNA profile in leptomeningeal metastasis patients [LM vs non-LM]

(Submitter supplied) This study aimed to identify specific CSF miRNAs for diagnosing and monitoring leptomeningeal metastasis with lung adenocarcinoma. In discovery phase, we performed miRNA microarray analysis in CSF samples from leptomeningeal metastasis patients and non-leptomeningeal metastasis controls.
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by array
Platform:
GPL25134
20 Samples
Download data: TXT, XLS
Series
Accession:
GSE125191
ID:
200125191
17.

Lost miRNA surveillance of NOTCH, IGFR pathway-road to sarcomagenesis

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array; Other
Platforms:
GPL15476 GPL10558
12 Samples
Download data
Series
Accession:
GSE48420
ID:
200048420
18.

Lost miRNA surveillance of NOTCH, IGFR pathway-road to sarcomagenesis [Illumina]

(Submitter supplied) The goal of this study was comparative analysis of differentially expressed miRNA and their targets in human chondrosarcoma JJ012 and chondrocytes C28 cell line(control) to elucidate the major signal transduction pathways deregulation in sarcomagenesis. Total RNA extraction was followed by the analysis of RNA quality and integrity, Exiqon human miRNA panel of 743 unique miRNA assays, Illumina microarray HT12 platform and qRT-PCR verification of targets were performed.189 downregulated and 147 upregulated miRNAs were detected when comparing chondrosarcoma cell line to control C 28 chondrocytes cell line using human Exiqon arrays with biological triplicates.3045 target genes in total were detected woth 587 common and 2458 unique target genes between upand downregulated miRNAs. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
6 Samples
Download data: TXT
Series
Accession:
GSE48418
ID:
200048418
19.

Lost miRNA surveillance of NOTCH, IGFR pathway-road to sarcomagenesis [Exiqon]

(Submitter supplied) The goal of this study was comparative analysis of differentially expressed miRNA and their targets in human chondrosarcoma JJ012 and chondrocytes C28 cell line (control) to elucidate the major signal transduction pathways deregulation in sarcomagenesis. Total RNA extraction was followed by the analysis of RNA quality and integrity, Exiqon human miRNA panel of 743 unique miRNA assays, Illumina microarray HT12 platform and qRT-PCR verification of targets were performed. more...
Organism:
Homo sapiens
Type:
Other
Platform:
GPL15476
6 Samples
Download data: TXT, XLS
Series
Accession:
GSE48396
ID:
200048396
20.

Whole transcriptome of Lewis lung carcinoma cells of Mus musculus

(Submitter supplied) Purpose: To study the alteration of whole transcriptome of Lewis lung carcinoma (LLC) cells after the decreasing of malignant properties of tumor by treatment of tumor-bearing mice with RNase A. Methods: Whole transcriptome profile of Lewis lung carcinoma before and after RNase A treatment were generated by deep sequencing using SOLiD 5.5. The sequence reads were mapped by Bioscope 1.3 software, differential expression was evaluated by Cufflinks v.2.0.1 package. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL15907
2 Samples
Download data: DIFF, TXT
Series
Accession:
GSE63758
ID:
200063758
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