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Home › Dataset Library › Transcription profiling of human H1299 non-small-cell lung cancer cells (parental H1299, H1299 cells which overexpress wild-type: EGFR-WT...

Dataset: Transcription profiling of human H1299 non-small-cell lung cancer cells (parental H1299, H1299 cells which overexpress wild-type: EGFR-WT and mutant EGFR: L858R) after EGF and Iressa stimulation

Controlled activation of epidermal growth factor receptor (EGFR) is systematically guaranteed at the molecular level, however aberrant...

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Controlled activation of epidermal growth factor receptor (EGFR) is systematically guaranteed at the molecular level, however aberrant activation of EGFR is frequently found in cancer. Transcription induced by EGFR activation often involves coordinated expression of genes that positively and negatively regulate the original signaling pathway, therefore alterations in EGFR kinase activity may reflect changes in gene expression associated with the pathway. In this study, we investigated transcriptional changes following EGF stimulation with or without the EGFR kinase inhibitor Iressa in H1299 human non-small-cell lung cancer cells (parental H1299, H1299 cells which overexpress wild-type: EGFR-WT and mutant EGFR: L858R). Our results clearly showed differences in transcriptional activity in the absence or presence of EGFR kinase activity, and genes sharing the same molecular functions showed distinct expression dynamics. The results showed particular enrichment of EGFR/ErbB signaling-related genes in a differentially expressed gene set, and significant protein expression of MIG6/RALT(ERRFI1), an EGFR negative regulator, was confirmed in L858R. High MIG6 protein expression was correlated with basal EGFR phosphorylation and inversely correlated with EGF-induced ERK phosphorylation levels. Investigation of NCI-60 cell lines showed that ERRFI1 expression was correlated with EGFR expression regardless of tissue type. These results suggest that cells accumulate MIG6 as an inherent negative regulator to suppress excess EGFR activity when basal EGFR kinase activity is considerably high. Taken together, an EGFR mutation can cause transcriptional changes to accommodate the activation potency of the original signaling pathway at the cellular level. Experiment Overall Design: H1299 human non-small cell lung cancer cells were stimulated by the growth hormone (epidermal growth factor (EGF)) or EGFR kinase inhibitor (Iressa). Control was set as non-treated cells.

Species:
human

Samples:
60

Source:
E-GEOD-11729

Updated:
Dec.12, 2014

Registered:
Sep.03, 2014


Factors: (via ArrayExpress)
Sample
GSE11729GSM297607
GSE11729GSM297608
GSE11729GSM297609
GSE11729GSM297610
GSE11729GSM297611
GSE11729GSM297612
GSE11729GSM297613
GSE11729GSM297614
GSE11729GSM297615
GSE11729GSM297616
GSE11729GSM297617
GSE11729GSM297618
GSE11729GSM297619
GSE11729GSM297620
GSE11729GSM297621
GSE11729GSM297622
GSE11729GSM297623
GSE11729GSM297624
GSE11729GSM297625
GSE11729GSM297626
GSE11729GSM297627
GSE11729GSM297628
GSE11729GSM297629
GSE11729GSM297630
GSE11729GSM297631
GSE11729GSM297632
GSE11729GSM297633
GSE11729GSM297634
GSE11729GSM297635
GSE11729GSM297636
GSE11729GSM297637
GSE11729GSM297638
GSE11729GSM297639
GSE11729GSM297640
GSE11729GSM297641
GSE11729GSM297642
GSE11729GSM297643
GSE11729GSM297644
GSE11729GSM297645
GSE11729GSM297646
GSE11729GSM297647
GSE11729GSM297648
GSE11729GSM297649
GSE11729GSM297650
GSE11729GSM297651
GSE11729GSM297652
GSE11729GSM297653
GSE11729GSM297654
GSE11729GSM297655
GSE11729GSM297656
GSE11729GSM297657
GSE11729GSM297658
GSE11729GSM297659
GSE11729GSM297660
GSE11729GSM297661
GSE11729GSM297662
GSE11729GSM297663
GSE11729GSM297664
GSE11729GSM297665
GSE11729GSM297666

Tags

  • basal
  • cancer
  • cell
  • hormone
  • lung
  • lung cancer
  • protein

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