A NOVEL MODEL FOR METASTASIS SUPPRESSION INVOLVING REGULATION OF NUCLEAR PRECURSOR MESSENGER-RNA STABILITY
- BR HENDERSON
- D MCDONALD
- S JONES
- RF KEFFORD
Affiliations: UNIV SYDNEY,WESTMEAD CTR,DEPT MED ONCOL,WESTMEAD,NSW 2145,AUSTRALIA.
- Published online on: February 1, 1995 https://doi.org/10.3892/ijo.6.2.483
Views: 0 (Spandidos Publications: | PMC Statistics: )
Total PDF Downloads: 0 (Spandidos Publications: | PMC Statistics: )
This article is mentioned in:
Our previous data correlated urokinase plasminogen activator (uPA) gene activation with metastasis in different rat mammary carcinomas, However, inconsistent with this was the suppression of the uPA gene in the metastatic rat mammary carcinoma cell line, BC1. We have now re-examined this cell line, selecting in vivo specifically for those BC1 cells capable of lung metastasis. We demonstrate that within the polyclonal BC1 cell line, it is possible to enrich for a metastatic sub-population which synthesizes 4 to 5-fold higher levels of uPA mRNA and enzyme activity. Therefore, the ability of a BC1 cell to metastasize appears to correlate with its escape from suppression of the uPA gene in this tumour. The results are consistent with the mechanism of uPA gene activation in metastatic DMBA-8 rat mammary tumour cells, and suggest a novel model of tumour progression based on regulation of pre-mRNA stability.