RGD Reference Report - Interleukin-24 induces expression of beta4 integrin but suppresses anchorage-independent growth of rat mammary tumor cells by a mechanism that is independent of beta4. - Rat Genome Database

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Interleukin-24 induces expression of beta4 integrin but suppresses anchorage-independent growth of rat mammary tumor cells by a mechanism that is independent of beta4.

Authors: Xuan, W  Li, YJ  Liu, G  Ben-David, Y  Archer, MC 
Citation: Xuan W, etal., Mol Cancer Res. 2009 Mar;7(3):433-42. Epub 2009 Mar 3.
RGD ID: 5147427
Pubmed: PMID:19258414   (View Abstract at PubMed)
DOI: DOI:10.1158/1541-7786.MCR-08-0252   (Journal Full-text)

Wistar-Furth rats develop multiple mammary adenocarcinomas following initiation with methylnitrosourea, whereas Copenhagen rats are resistant to the development of mammary tumors. We have previously isolated cell lines from tumors induced in resistant Copenhagen x Wistar-Furth F(1) rats by infusion of a retrovirus harboring v-Ha-ras directly into the main mammary ducts. Some of the cell lines were able to grow in soft agar, but a significant number did not display anchorage-independent growth. Here, we compared by microarray analysis genes that are differentially expressed in these cell lines. The expression of interleukin-24 (IL-24) and beta(4) integrin was highly correlated with the inability of cells to grow in soft agar. Ectopic expression of IL-24 in anchorage-independent cells inhibited their growth in monolayer culture, in soft agar, and in nude mice in vivo and inhibited their ability to migrate and invade in in vitro assays. Furthermore, growth suppression by IL-24 was associated with the transcriptional up-regulation of p27(Kip1) via the activation of Stat3. We showed, for the first time, that beta(4) integrin is a downstream target of IL-24. However, beta(4) does not play a direct role in regulating the proliferative capacity of rat mammary tumor cells. Our results show that IL-24 suppresses the growth of rat mammary carcinoma cells and may play a role in the resistance of Copenhagen rats to mammary carcinogenesis.



Gene Ontology Annotations    Click to see Annotation Detail View

Biological Process

  
Object SymbolSpeciesTermQualifierEvidenceWithNotesSourceOriginal Reference(s)
Il24Ratnegative regulation of cell migration  IDA  RGD 
Il24Ratnegative regulation of cell population proliferation  IDA  RGD 
Il24Ratpositive regulation of protein modification process  IDA tyrosine phosphorylation of STAT proteinRGD 
Il24Ratserine phosphorylation of STAT protein  IDA  RGD 

Objects Annotated

Genes (Rattus norvegicus)
Il24  (interleukin 24)


Additional Information