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Links from GEO DataSets

Items: 18

1.

Effect of chronic low dose of cadmium chloride exposure on long non-coding RNA expression in human bronchial epithelial BEAS-2B cells

(Submitter supplied) BEAS-2B cells were continuously exposed to 2.5 uM of cadmium chloride for 9 months and the expresssion of lncRNAs were analyzed by lncRNA microarray analysis.
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by array
Platform:
GPL21827
6 Samples
Download data: TXT
Series
Accession:
GSE175472
ID:
200175472
2.

m6A-mRNA&lncRNA Epitranscriptomic Microarray

(Submitter supplied) Total RNA samples from human bronchial epithelial BEAS-2B passage-matched control cells and Cr(VI)-transofmred BEAS-2B cells were submitted to ArraySatr for total RNA m6A epitranscriptomic microarray analysis
Organism:
Homo sapiens
Type:
Other
Platform:
GPL25759
6 Samples
Download data: TXT, XLSX
Series
Accession:
GSE186605
ID:
200186605
3.

Microarray analysis of gene expression in human bronchial epithelial cells exposed to arsenic, BaP alone or arsenic plus BaP

(Submitter supplied) Human bronchial epithelial cell BEAS-2B cells were continuously exposed to a vehicel control (DMSO), arsenic (NaAsO2, 1 uM), BaP (2.5 um) alone or arsenic plus BaP for 30 weeks. At the end of exposure, cells were collected and total RNA was extracted for microarray analysis.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL21827
12 Samples
Download data: TXT
Series
Accession:
GSE149605
ID:
200149605
4.

The lncRNA microarray analysis of 16HBE cell treated with PM2.5 samples in Guangzhou

(Submitter supplied) In order to assess the alteration of lncRNA expression in 16HBE cell treated with PM2.5 samples, we determined the lncRNA expression profiles in 16HBE cell treated with PBS (control group) and PM2.5 samples (low dose 125 μg/mL and high dose 500 μg/mL) using lncRNA Microarray.
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by array
Platform:
GPL21651
3 Samples
Download data: GPR
Series
Accession:
GSE79570
ID:
200079570
5.

Meg3 regulated genes in pancreatic beta cells

(Submitter supplied) Meg3 is a long non-coding RNA. It's target genes are unknown. The mouse pancreatic beta cell line MIN6-4N was used to assess the expression of genes upon stable Meg3 overexpression
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL10740
6 Samples
Download data: CEL
Series
Accession:
GSE57716
ID:
200057716
6.

Comparison of gene expression profiles in chromate transformed BEAS-2B cells

(Submitter supplied) We established chromate transformed cell lines by chronic exposure of normal human bronchial epithelial BEAS-2B cells to low doses of hexavalent chromium followed by anchorage-independent growth. The gene expression profiles were analyzed in the established cell lines. The gene expression profiles from six chromate transformed cell lines were remarkably similar to each other yet differed significantly from that of either control cell line or normal Beas-2B cells. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6244
10 Samples
Download data: CEL
Series
Accession:
GSE24025
ID:
200024025
7.

Expression data from different expressed genes(DEGs) in human esophageal squamous cell carcinoma(ESCC) EC109 cells transfected with empty lentiviral vector(Lv-NC) or lentiviral vector carrying MEG3(Lv-MEG3)

(Submitter supplied) Maternally expressed gene 3 (MEG3), a member of lncRNAs, has tumor-suppressor properties and is downregulated in the majority of malignancies. MEG3 was found to suppress some sorts of tumors through regulating epithelial mesenchymal transformation,inducing cell cycle arrest,triggering apoptosis and so on. We used microarrays to investigate the possible regulatory mechanism of MEG3 in ESCC cell line.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL15207
6 Samples
Download data: CEL
Series
Accession:
GSE142036
ID:
200142036
8.

Whole genome expression profile of lung epithelial cells following chronic arsenic exposure

(Submitter supplied) This study chronically exposed human lung epithelial BEAS-2B cells to low-dose arsenic trioxide in vitro to elucidate cancer promoting gene signaling networks (GSNs) associated with As-transformed (B-As) cells. Following a six month exposure, exposed cells were assessed for enhanced cell proliferation, colony formation, invasion ability and in vivo tumor formation compared to control cell lines. Collected mRNA was subjected to whole genome expression microarray profiling followed by in silico Ingenuity Pathway Analysis (IPA) to identify lung carcinogenesis modes of action. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS5498
Platform:
GPL6480
7 Samples
Download data: TXT
Series
Accession:
GSE33520
ID:
200033520
9.
Full record GDS5498

Arsenic effect on lung epithelial cell line

Analysis of BEAS-2B lung epithelial cells treated with 2.5 uM arsenic trioxide for 6 months. Chronic arsenic exposure increases lung cancer risk. Results provide insight into the molecular mechanisms underlying lung carcinogenesis associated with arsenic exposure.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 2 agent sets
Platform:
GPL6480
Series:
GSE33520
7 Samples
Download data: TXT
10.

The rat lncRNA microarray analysis of the 8 samples from control and NNK treatment group

(Submitter supplied) In order to assess the alteration in lncRNA expression in rat lung carcinogenesis induced by NNK, we determined the lncRNA expression profiles in 3 rat lung tumor samples and matched normal lung tissues and 2 blood samples from the control and NNK treatment group in the 95th week using Arraystar Rat lncRNA Microarray.
Organism:
Rattus norvegicus
Type:
Non-coding RNA profiling by array
Platform:
GPL15690
8 Samples
Download data: TXT
Series
Accession:
GSE68967
ID:
200068967
11.

Transcriptome analyses in normal prostate epithelial cells following exposure to low-dose cadmium

(Submitter supplied) BACKGROUND: Cadmium is implicated in prostate carcinogenesis, but its oncogenic action remains unclear. OBJECTIVES: In this study we aimed to decipher changes in cell growth and the transcriptome in an immortalized human normal prostate epithelial cell line (NPrEC) following exposure to low-dose Cd. METHODS: Synchronized NPrEC cells were exposed to different doses of Cd and assayed for cell viability and cell-cycle progression. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS3354
Platform:
GPL570
19 Samples
Download data: CEL
Series
Accession:
GSE9951
ID:
200009951
12.
Full record GDS3354

Low-dose cadmium effect on prostate epithelial cells: time course

Analysis of immortalized normal prostate epithelial cell line NPrEC exposed to non-cytotoxic levels of cadmium (2.5uM CdCl2) for up to 32hrs. Cadmium is implicated in prostate carcinogenesis. Results provide insight into mechanisms underlying the initiation of carcinogenesis by Cd in the prostate.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 2 agent, 5 time sets
Platform:
GPL570
Series:
GSE9951
19 Samples
Download data: CEL
13.

LncRNA Tuna is activated in cadmium-induced placental insufficiency and drives the NRF2-mediated oxidative stress response.

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens; Mus musculus
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL24247 GPL24676
24 Samples
Download data
Series
Accession:
GSE233282
ID:
200233282
14.

LncRNA Tuna is activated in cadmium-induced placental insufficiency and drives the NRF2-mediated oxidative stress response [human Jeg3]

(Submitter supplied) Cadmium (Cd) is a toxic heavy metal found throughout the environment and one of the top ten toxicants of major public health concern identified by the World Health Organization.InuteroCd exposure causes fetal growth restriction, malformation, and spontaneous abortion; however, the mechanisms by which Cd impacts these outcomes are poorly understood. Cd accumulates in the placenta, suggesting that these negative outcomes may be a consequence of disrupted placental function and placental insufficiency. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
16 Samples
Download data: CSV
Series
Accession:
GSE233281
ID:
200233281
15.

LncRNA Tuna is activated in cadmium-induced placental insufficiency and drives the NRF2-mediated oxidative stress response [mouse]

(Submitter supplied) Cadmium (Cd) is a toxic heavy metal found throughout the environment and one of the top ten toxicants of major public health concern identified by the World Health Organization.InuteroCd exposure causes fetal growth restriction, malformation, and spontaneous abortion; however, the mechanisms by which Cd impacts these outcomes are poorly understood. Cd accumulates in the placenta, suggesting that these negative outcomes may be a consequence of disrupted placental function and placental insufficiency. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
8 Samples
Download data: CSV
Series
Accession:
GSE233252
ID:
200233252
16.

Stem cell function and sensitivity to genotoxic stress is controlled by protein translation rates

(Submitter supplied) Whether protein synthesis and cellular stress response pathways interact to control stem cell functions is currently unknown. Here, we show that skin stem cells synthesise less protein than their immediate progenitors in vivo, even when forced to proliferate in a tumour model. Our analyses reveal that activation of stress response pathways drives both a global reduction of protein synthesis and altered translation of specific mRNAs that together promote stem cell functions and tumourigenesis. more...
Organism:
Mus musculus
Type:
Methylation profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing; Expression profiling by high throughput sequencing; Other
Platform:
GPL9250
28 Samples
Download data: BEDGRAPH
Series
Accession:
GSE72067
ID:
200072067
17.

Ribosome Profiling of mouse skin squamous tumours

(Submitter supplied) Purpose: Ribosome profiling has revolutionized systems-based analysis and which produces a “global snapshot” of all the ribosomes translationally active in a cell at a particular moment. The goals of this study are to first apply ribosome profiling to in vivo samples for the first time and in particular to stem cells and tumours and second to determine which mRNAs are being actively translated in these particular situations. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL9250
12 Samples
Download data: BEDGRAPH
Series
Accession:
GSE72066
ID:
200072066
18.

Transfer RNA (tRNA) processing and RNA m5C-methylation profiles of mouse skin squamous tumours

(Submitter supplied) Purpose: High-throughput RNA sequencing has accelerated discovery of the complex regulatory roles of small RNAs, such those derived from tRNAs. Also recent advances in high-throughput RNA sequencing has revealed the complex RNA modification landscape and the complex role these nucleosides modifactions have in cell signalling, stem cell biology, development and cancer. The goal of this study is to establish how m5C-tRNA methylation and tRNA-derived small RNAs can affect stem cell fucntion in cancer. more...
Organism:
Mus musculus
Type:
Methylation profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing
Platform:
GPL9250
16 Samples
Download data: BEDGRAPH
Series
Accession:
GSE72065
ID:
200072065
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