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Gene set: EMT_DOWN_JECHLINGER (C2:PERT:0008)
Standard nameEMT_DOWN_JECHLINGER
Systematic nameC2:PERT:0008
Brief descriptionGenes downregulated for epithelial plasticity in tumor progression
CategoryC2: Curated
Sub-categoryPERT: Experimental pertuberation
Full description or Abstract
Epithelial-to-mesenchymal transition (EMT), a switch of polarized
epithelial cells to a migratory, fibroblastoid phenotype, is increasingly
considered as an important event during malignant tumor progression
and metastasis. To identify molecular players involved in EMT
and metastasis, we performed expression profiling of a set of
combined in vitro/in vivo cellular models, based on clonal, fully
polarized mammary epithelial cells. Seven closely related cell
pairs were used, which were modified by defined oncogenes and/or
external factors and showed specific aspects of epithelial plasticity
relevant to cell migration, local invasion and metastasis. Since
mRNA levels do not necessarily reflect protein levels in cells,
we used an improved expression profiling method based on polysome-bound
RNA, suitable to analyse global gene expression on Affymetrix
chips. A substantial fraction of all regulated genes was found
to be exclusively controlled at the translational level. Furthermore,
profiling of the above multiple cell pairs allowed one to identify
small numbers of genes by cluster analysis, specifically correlating
gene expression with EMT, metastasis, scattering and/or oncogene
function. A small set of genes specifically regulated during EMT
was identified, including key regulators and signaling pathways
involved in cell proliferation, epithelial polarity, survival
and trans-differentiation to mesenchymal-like cells with invasive
behavior. 
Publication URL14562044
External linksna
Keywords & MeSH headingsNeoplastic,Epithelial Cells,Animal/cytology/pathology,Gene Expression Profiling,Cell Transformation,Messenger/genetics,Human,Support,ras,Translation,Genes,genetics,Cell Differentiation,Mice,Genetic,Cluster Analysis,Cell Line,Mesoderm,RNA,Breast Neoplasms/genetics/pathology,Mammary Glands,Polyribosomes/genetics,Female,Transcription,pathology,Neoplasm Invasiveness,Gene Expression Regulation,physiology
OrganismHuman
Contributed byBroad Institute
Source platformMu11KsubA
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Genes

40 genes, 40 accessions (Toggle view)

AccessionGeneTitleLinks
FBP2
HMMR
STAT5A
FLNA
BCL6
ATF3
MYH9
FOSB
TIMP3
RARA
IRF6
AMD1
F3
PKP1
EGR1
TGM2
ATP1A1
DUSP1
ITPR1
SGK
CTGF
KITLG
SERPINB5
ACTN4
NUMB
JUP
PADI2
VAMP8
KLF2
TACSTD1
TGFB3
ARHGEF1
NNT
THBS1
CDH1
TIAM1
GRB7
ITGB5
CTSH
EGR2


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