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Homo sapiens

ABSTRACT: Genome-wide maps of NME2 in A549 lung adenocarcinoma cells.

OTHER RELATED OMICS DATASETS IN: E-GEOD-18182

PROVIDER: PRJNA173992 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR547939.fastq.gz	Fastqsanger.gz
	SRR547940.fastq.gz	Fastqsanger.gz
	SRR547941.fastq.gz	Fastqsanger.gz
	SRR547942.fastq.gz	Fastqsanger.gz
	SRR547943.fastq.gz	Fastqsanger.gz

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Characterization of the transcriptional roles of NME2

Project description:This SuperSeries is composed of the following subset Series: GSE18182: Expression profile of lung adenocarcinoma, A549 cells following targeted depletion of non metastatic 2 (NME2/NM23 H2) GSE18284: Genomic binding sites of non-metastatic 2 (NME2) across promoters in lung cancer A549 cells Refer to individual Series

2011-02-08 | E-GEOD-18285 | biostudies-arrayexpress

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Project description:Expression profile of lung adenocarcinoma, A549 cells following induction of non metastatic 2 (NME2/NM23 H2)

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Project description:Expression profile of lung adenocarcinoma, A549 cells following targeted depletion of non metastatic 2 (NME2/NM23 H2)

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Project description:Genome-wide maps of histone H3K27 acetylation in A549 and MSR-A549 cells.

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Project description:Expression data from A549 lung adenocarcinoma cells and TUSC3 knocked out A549 cells

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Project description:Nucleosome positioning in A549 cells before/after NME2 induction

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CIT - Homo sapiens - APUP - Genomic aberrations in Lung Adenocarcinoma in Never Smokers

Project description:41 lung adenocarcinoma from never-smokers hybridized on Illumina SNP arrays on 13 HumanCNV370-Quadv3 chips. High-resolution array comparative genomic hybridization analysis of lung adenocarcinoma in 41 never smokers for identification of new minimal common regions (MCR) of gain or loss. The SNP array analysis validated copy-number aberrations and revealed that RB1 and WRN were altered by recurrent copy-neutral loss of heterozygosity.The present study has uncovered new aberrations containing cancer genes. The oncogene FUS is a candidate gene in the 16p region that is frequently gained in never smokers. Multiple genetic pathways defined by gains of MYC, deletions of RB1 and WRN or gains on 7p and 7q are involved in lung adenocarcinoma in never smokers. A 'Cartes d'Identite des Tumeurs' (CIT) project from the French National League Against Cancer (http://cit.ligue-cancer.net) 41 samples hybridized on Illumina SNP arrays. Submitter : Fabien PETEL petelf@ligue-cancer.net . Project leader : Pr Pierre FOURET pierre.fouret@psl.aphp.fr

2011-07-28 | E-TABM-1169 | biostudies-arrayexpress

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Project description:Genomic binding sites of non-metastatic 2 (NME2) across promoters in lung cancer A549 cells

| PRJNA123513 | ENA

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Project description:Knockdown of CUL3 and PTEN in A549 lung adenocarcinoma cells

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Expression profile of lung adenocarcinoma, A549 cells following targeted depletion of non metastatic 2 (NME2/NM23 H2)

Project description:Non-metastatic 2 (NME2) is an established metastases suppressor in multiple human cancer types. However, the molecular mechanisms of NME2 action remain insufficiently resolved. We recently validated the transcription regulatory activity of NME2 with respect to control of proto-oncogene c-MYC expression. We hypothesized that large scale transcriptional potential of NME2 may be at the core of metastases suppression by NME2. Using a combination of high throughput genomic assays such as chromatin immunoprecipitation coupled to promoter array hybridization (ChIP-chip) and gene expression profiling, we characterized the transcriptional roles of NME2. Specifically, we found a set of NME2 target genes which changed expression upon selective depletion of NME2 in a lung cancer cell line, A549. The analysis of gene expression suggested control of various biological pathways esp. cell adhesion and apoptosis by NME2 target genes which could be important in regulation of metastases. For transcriptome analysis, total RNA was purified from A549 cells transiently silenced for NME2 (siRNA duplex against NME2/ NM23 H2(Santa Cruz)) or transfected with control siRNA duplexes. Isolated RNA was converted to cDNA, transcribed in vitro to synthesize biotinylated cRNA, and hybridized to Affymetrix HG-U133 plus 2.0 GeneChip oligonucleotide microarrays, according to manufacturer‚Äö√Ñ√¥s instructions. Three biological replicates were averaged and significance analysis performed using GCOS (P <0.005 of fold change).

2011-02-08 | E-GEOD-18182 | biostudies-arrayexpress

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