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Table 1 Major functional groups overrepresented among state-change genes and corresponding overrepresented TREs. The groups are presented according to the order of significance identified by DAVID. Overrepresented TREs marked in bold are either "off-on" TFs or increased their level; regular – not present in Panomics set; italics – not present under either condition.

From: From microarray to biology: an integrated experimental, statistical and in silico analysis of how the extracellular matrix modulates the phenotype of cancer cells

Functional group

Number of genes

Major Gene Ontologies

Overrepresented TREs

Gene expression, RNA processing and protein synthesis

12

73

Transcription factors

 

7

5

Translation initiation factors

v-Maf, SOX-9, FOXJ2, CP2, HFH-3, Elk-1, NRF-2, AREB6

9

6

RNA processing – ribosome biogenesis

NGFI-C, GR, HNF-4, YY1, Elk-1, NRF-2, v-Myb, NF-κB, TATA, c-Myc

11

8

Zinc binding

MIF-1, Tax/CREB

Cell signaling proteins

3

16

G-protein receptor

 

2

7

GABA receptor/ion channels

N-Myc

6

9

Ion channels, K

 

Post-translational modification and regulatory control

8

5

Glycosyltransferases

 

10

28

Kinases

CDP, CR3+HD, CRE-BP1, CCAAT

Cell-ECM adhesion

4

4

Cadherins

HNF-3β, CDP CR3+HD, E2, NF-κB, USF

Immune function associated with suppression of effector T-cells

1

15

Transmembrane immunoglobulin-like proteins

NF-κB, v-Maf, RSRFC4, FOXJ2, AP-1, Pax-4, USF, CDP, Brn-2

Transmembrane proteins of unknown significance

5

14

Transmembrane proteins

AP-1