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Gene set: RAS_STROMA_UP_CROONQUIST (C2:PERT:0069)
Standard nameRAS_STROMA_UP_CROONQUIST
Systematic nameC2:PERT:0069
Brief descriptionGenes upregulated in multiple myeloma cells with N-ras-activating mutations versus those co-cultured with bone marrow stromal cells.
CategoryC2: Curated
Sub-categoryPERT: Experimental pertuberation
Full description or Abstract

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ANBL-6, a myeloma cell line, proliferates in response to interleukin
6 (IL-6) stimulation, coculture with bone marrow stromal cells,
and when harboring a constitutively active mutant N-ras gene.
Eighteen samples, including 4 IL-6-treated, 3 mutant N-ras-transfected,
3 normal stroma-stimulated, 2 multiple myeloma (MM) stroma-stimulated,
and 6 untreated controls were profiled using microarrays interrogating
12 626 genes. Global hierarchical clustering analysis distinguished
at least 6 unique expression signatures. Notably, the different
stimuli altered distinct functional gene programs. Class comparison
analysis (P =.001) revealed 138 genes (54% involved in cell cycle)
that distinguished IL-6-stimulated versus nontreated samples.
Eighty-seven genes distinguished stroma-stimulated versus IL-6-treated
samples (22% encoded for extracellular matrix [ECM] proteins).
A total of 130 genes distinguished N-ras transfectants versus
IL-6-treated samples (26% involved in metabolism). A total of
157 genes, 20% of these involved in signaling, distinguished N-ras
from stroma-interacting samples. All 3 stimuli shared 347 genes,
mostly of metabolic function. Genes that distinguished MM1 from
MM4 clinical groups were induced at least by one treatment. Notably,
only 3 genes (ETV5, DUSP6, and KIAA0735) are uniquely induced
in mutant ras-containing cells. We have demonstrated gene expression
patterns in myeloma cells that distinguish an intrinsic genetic
transformation event and patterns derived from both soluble factors
and cell contacts in the bone marrow microenvironment. 
Publication URL12791645
External linksna
Keywords & MeSH headingsCell Communication/physiology,Coculture Techniques,Neoplastic/drug effects/physiology,Non-P.H.S.,Gene Expression Profiling,P.H.S.,Comparative Study,pharmacology,Phenotype,Multiple Myeloma,Humans,Tumor Cells,ras Proteins/metabolism,Stromal Cells,ras,Genes,genetics,Gene Expression Regulation,cytology,physiology,Cell Division/drug effects,Interleukin-6,Mitogen-Activated Protein Kinases/metabolism,Cultured/cytology
OrganismHuman
Contributed byKate Stafford
Source platformSeq_Accession
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Genes

21 genes, 25 accessions (Toggle view)

AccessionGeneTitleLinks
Z54367PLEC1plectin 1, intermediate filament binding protein 500kDaSource|GeneCards
X04011CYBBcytochrome b-245, beta polypeptide (chronic granulomatous disease)Source|GeneCards
U04343CD86CD86 antigen (CD28 antigen ligand 2, B7-2 antigen)Source|GeneCards
AF070641ETV1ets variant gene 1Source|GeneCards
AI660656
AB002351DMNdesmuslinSource|GeneCards
M62397MCCmutated in colorectal cancersSource|GeneCards
AF055004IQSEC1IQ motif and Sec7 domain 1Source|GeneCards
X02751NRASneuroblastoma RAS viral (v-ras) oncogene homologSource|GeneCards
AI142565
X81438AMPHamphiphysin (Stiff-Man syndrome with breast cancer 128kDa autoantigen)Source|GeneCards
M80335
D21205TRIM25tripartite motif-containing 25Source|GeneCards
AL512715ARHGEF2rho/rac guanine nucleotide exchange factor (GEF) 2Source|GeneCards
AF043722RASGRP2RAS guanyl releasing protein 2 (calcium and DAG-regulated)Source|GeneCards
AB018278SV2Bsynaptic vesicle glycoprotein 2BSource|GeneCards
J04430ACP5acid phosphatase 5, tartrate resistantSource|GeneCards
U48807DUSP4dual specificity phosphatase 4Source|GeneCards
M55067NCF1neutrophil cytosolic factor 1 (47kDa, chronic granulomatous disease, autosomal 1)Source|GeneCards
S71326CEACAM1carcinoembryonic antigen-related cell adhesion molecule 1 (biliary glycoprotein)Source|GeneCards
AB020689KIAA0882KIAA0882 proteinSource|GeneCards
X99802ZYG11BLzyg-11 homolog B (C. elegans)-likeSource|GeneCards
U20350
AB013382DUSP6dual specificity phosphatase 6Source|GeneCards
Y14737IGHG3immunoglobulin heavy constant gamma 3 (G3m marker)Source|GeneCards


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