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Links from GEO DataSets

Items: 20

1.

Gene Expression Patterns that Predict Sensitivity to Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitors in Lung Cancer Cell Lines and Human Lung Tumors

(Submitter supplied) Global gene expression data were generated from cultured non small cell lung cancer cell lines (NSCLC), normalized using MAS 5.0, filtered and used to predict response of cells to EGFR inhibition
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL96
48 Samples
Download data: CEL
Series
Accession:
GSE31625
ID:
200031625
2.

Clinical Utility of Patient Derived Xenografts to Determine Biomarkers of Prognosis and Map Resistance Pathways in EGFR-Mutant Lung Adenocarcinoma

(Submitter supplied) PURPOSE: Although epidermal growth factor receptor (EGFR) mutated adenocarcinomas initially have very high response rates to EGFR tyrosine kinase inhibitors (TKIs), most atients eventually develop resistance. Patient derived xenografts (PDXs) are considered preferred preclinical models to study the biology of patient tumors. EGFR-mutant PDX models may be valuable tools to study the biology of these tumors and to elucidate mechanisms of resistance to EGFR-targeted therapies. more...
Organism:
Homo sapiens; Mus musculus
Type:
Expression profiling by array
Platform:
GPL14951
25 Samples
Download data: TXT
Series
Accession:
GSE63685
ID:
200063685
3.

Gefitinib sensitivity in NSCLC cell lines

(Submitter supplied) Eleven NSCLC cell lines with widely divergent gefitinib sensitivities were compared using gene expression. Genes associated with gefitinib response were used to classify additional NSCLC lines with unknown gefitnib sensitivity. A subset of the test set data was tested for gefitinib sensitivity, and results correlated strongly with the gene expression-based predictions All eleven training set lines, and seven test set lines had both HGU133A and B chips done, while other test set lines had only HGU133As. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Datasets:
GDS2297 GDS2298
Platforms:
GPL97 GPL96
63 Samples
Download data
Series
Accession:
GSE4342
ID:
200004342
4.
Full record GDS2298

Gefitinib effect on various non-small cell lung cancer cell lines (HG-U133B)

Analysis of baseline non-small cell lung cancer (NSCLC) cell lines with a broad range of sensitivity to the anticancer drug gefitinib. Gefitinib is an epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI). Results used to define a gene expression signature of gefitinib sensitivity.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 18 cell line, 3 other, 2 protocol sets
Platform:
GPL97
Series:
GSE4342
18 Samples
Download data
5.
Full record GDS2297

Gefitinib effect on various non-small cell lung cancer cell lines (HG-U133A)

Analysis of baseline non-small cell lung cancer (NSCLC) cell lines with a broad range of sensitivity to the anticancer drug gefitinib. Gefitinib is an epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI). Results used to define a gene expression signature of gefitinib sensitivity.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 41 cell line, 4 other, 2 protocol sets
Platform:
GPL96
Series:
GSE4342
45 Samples
Download data
6.

Expression data from EGFR mutant transgenic mice

(Submitter supplied) We performed mRNA expression profiling of lung tumors from C/L858R, C/T790M, and C/L+T mice and from corresponding normal lung tissue.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
24 Samples
Download data: CEL
Series
Accession:
GSE17373
ID:
200017373
7.

An epithelial-mesenchymal transition (EMT) gene signature predicts resistance to erlotinib and PI3K pathway inhibitors and identifies Axl as a novel EMT marker in non-small cell lung cancer.

(Submitter supplied) Epithelial/mesenchymal transition (EMT) is associated with loss of cell adhesion molecules, such as E-cadherin, and increased invasion, migration, and proliferation in epithelial cancers. In non-small cell lung cancer (NSCLC), EMT is associated with greater resistance to EGFR inhibitors. However, its potential to predict response to other targeted drugs or chemotherapy has not been well characterized. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6244
131 Samples
Download data: CEL
Series
Accession:
GSE33072
ID:
200033072
8.

Expression profiling of lung cancer cell lines (UTSW Lung Panel V2)

(Submitter supplied) Epithelial/mesenchymal transition (EMT) is associated with loss of cell adhesion molecules, such as E-cadherin, and increased invasion, migration, and proliferation in epithelial cancers. In non-small cell lung cancer (NSCLC), EMT is associated with greater resistance to EGFR inhibitors. However, its potential to predict response to other targeted drugs or chemotherapy has not been well characterized. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL13376
69 Samples
Download data: TXT
Series
Accession:
GSE32989
ID:
200032989
9.

Expression profiling of lung cancer cell lines

(Submitter supplied) Purpose: To determine the 8-week disease control rate (DCR) of sorafenib monotherapy in patients with advanced non-small-cell lung cancer (NSCLC) in the BATTLE trial. Methods: Patients with pre-treated NSCLC, ECOG performance status (PS) 0-2, consented to biopsies to test for biomarker assessment. Sorafenib was given at 400 mg orally twice daily until tumor progression or an unacceptable toxicity. Tumor evaluations were performed at baseline and every 8 weeks. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platforms:
GPL10558 GPL6884
222 Samples
Download data: TXT
Series
Accession:
GSE32036
ID:
200032036
10.

Gene expression-signatures for non-small cell lung cancer patients with different EGFR muational status.

(Submitter supplied) To identify a plasma miRNA panel that could help to separate NSCLC patients with EGFR sensitive mutations and wild-type EGFR, plasma samples of 3 EGFR19DEL, 3 EGFRp.L858R, and 3 EGFRWT patients with NSCLC and 4 HCs were selected for Agilent miRNA microarray analysis to detect differences in the expression levels of circulating miRNAs (n = 2,568) between the above cohorts.
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by array
Platform:
GPL21576
13 Samples
Download data: TXT, XLS
Series
Accession:
GSE93300
ID:
200093300
11.

Microarray expression profile of long noncoding RNAs in EGFR-TKI resistance of lung adenocarcinoma

(Submitter supplied) Lung adenocarcinoma cells harboring epidermal growth factor receptor (EGFR) mutations are sensitive to EGFR tyrosine kinase inhibitors (TKIs). Prolonged cancer treatment will induce the development of acquired resistance to EGFR TKI. To gain insight into the molecular mechanisms of EGFR-TKIs resistance, we generate EGFR-TKI-resistant HCC827-8-1 cells to be analyzed by microarray with their parental HCC827cells.
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by array
Platform:
GPL21096
6 Samples
Download data: TXT
Series
Accession:
GSE74575
ID:
200074575
12.

Gene Expression Regulation by Lung Cancer Oncogenes

(Submitter supplied) To characterize gene expression changes induced by oncogenes implicated in human lung adenocarcinoma, we analyzed the whole transcriptome of NIH3T3 cells expressing mutant EGFR (exon 19 deletion) or wild-type EGFR. Expression levels of several genes from this list were validated by quantitative RT-PCR using the same RNA samples.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL10787
4 Samples
Download data: TXT
Series
Accession:
GSE104494
ID:
200104494
13.

Axl mediates acquired resistance of head and neck cancer cells to the epidermal growth factor receptor inhibitor erlotinib

(Submitter supplied) Elevated expression and activity of the epidermal growth factor receptor (EGFR) is associated with development and progression of head and neck cancer (HNC) and a poor prognosis. Clinical trials with EGFR tyrosine kinase inhibitors (TKIs; eg. erlotinib) have been disappointing in HNC. To investigate the mechanisms mediating resistance to these agents, we developed a HNC cell line (HN5-ER) with acquired erlotinib resistance. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
6 Samples
Download data: TXT
Series
Accession:
GSE49135
ID:
200049135
14.

Genomic CpG methylation and TKI-response of the patient with advanced stage lung adenocarcinoma

(Submitter supplied) The DNA methylation signature involved 87 differentially methylated regions (DMR) that distinguished patients’ response to EGFR-TKIs. The methylation level of HOXB9 (cg13643585) which was negatively correlated with gene expression and annotated as function of transcription factor displayed 88% and 92% of sensitivity with respect to objective response rate (ORR, OR=9.25, p=0.0002) and disease control rate (DCR, OR=6.64, p=0.0009), respectively. more...
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL13534
79 Samples
Download data: CSV
Series
Accession:
GSE147377
ID:
200147377
15.

Gene expression data for pathological stage I-II lung adenocarcinomas

(Submitter supplied) Identification of genes up-regulated in ALK-positive and EGFR/KRAS/ALK-negative lung adenocarcinomas. To elucidate molecular characteristics of lung adenocarcinomas (ADCs) with ALK mutations and those without EGFR, KRAS and ALK mutations, 226 primary lung ADCs of pathological stage I-II, examined for the status of EGFR, KRAS and ALK mutations, were subjected to genome-wide expression profiling, and genes up-regulated in lung ADCs with ALK mutations and those without EGFR, KRAS and ALK mutations were identified. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
246 Samples
Download data: CEL
Series
Accession:
GSE31210
ID:
200031210
16.

Expression data from the subclones of Lewis Lung Carcinoma (LLC) cells

(Submitter supplied) Medium conditioned by LLC cells stimulates thermogenic gene expression when added onto primary adipocytes. We generated single cell colonies from parental LLC cells. Media conditioned by the subclones stimulated thermogenic gene expression in primary adipocytes at varying degrees. Subclones 2, 3, 6 and 28 produce significantly larger amount of thermogenic activity than the subclones 18, 19, 23 and 24. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
23 Samples
Download data: CEL, CHP
Series
Accession:
GSE57797
ID:
200057797
17.

Translational application of pharmacogenomics for refractory lung cancer

(Submitter supplied) Patient-derived cells (PDC) recapitulate the characteristics of lung cancer and its therapeutic response. We collected cancer cells of patients to receive various chemotherapy and performed integrative analysis for pharmachogenomics.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
102 Samples
Download data: TXT
18.

Gene profiling, mutations and expression of epidermal growth factor receptor in androgen-dependent prostate cancer

(Submitter supplied) We analyzed mutations in Epidermal Growth Factor Receptor (EGFR) Tyrosine kinase (TK) domain, EGFR expression and gene profiling in prostate carcinoma (PC) in order to find out molecular prognostic markers and supply a proof for EGFR targeted therapies. 100 glyofixx-fixed, paraffin-embedded PC specimens were recovered after radical prostatectomy from locally advanced PC patients. Exons from 18 to 21 of EGFR TK domain were amplified and sequenced. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL887
65 Samples
Download data: TXT
Series
Accession:
GSE16120
ID:
200016120
19.

Analysis of ETS gene expression patterns uncovers novel ETS mediated gene silencing pathways in prostate cancers

(Submitter supplied) Deregulated expression of ETS transcription factors with oncogenic and tumor suppressor function occurs frequently in prostate cancer leading to profound alterations of the cancer transcriptome. By integrating genomic and functional studies we identified key targets of the aberrantly expressed ETS factors, ERG and ESE3. Altered expression of ETS factors led to the induction of the polycomb group protein EZH2 and silencing of the tumor suppressor Nkx3.1. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL887
67 Samples
Download data: TXT
Series
Accession:
GSE14206
ID:
200014206
20.

Coordinated over-expression of genes in the EGFR pathway predicts sensitivity to EGFR inhibition in pancreatic cancer

(Submitter supplied) Tumors from pancreatic cancer specimens obtained at surgery were used for efficacy testing and biologic analysis Keywords: Pharmacogenetics
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
36 Samples
Download data: CEL
Series
Accession:
GSE9599
ID:
200009599
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