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TNF-alpha and IFN-gamma down-regulate the expression of the metastasis-associated bi-functional 37LRP/p40 gene and protein in transformed keratinocytes.

作者信息

Clausse N, van den Brûle F, Delvenne P, Jacobs N, Franzen-Detrooz E, Jackers P, Castronovo V

机构信息

Metastasis Research Laboratory, Sart Tilman, Liège, B-4000, Belgium.

出版信息

Biochem Biophys Res Commun. 1998 Oct 20;251(2):564-9. doi: 10.1006/bbrc.1998.9431.

DOI:10.1006/bbrc.1998.9431
PMID:9792813
Abstract

The 37 LRP/p40 molecule is a bi-functional protein in which expression is increased in a large variety of cancers in association with their metastatic phenotype. Here we present the first data concerning the 37 LRP/p40 gene promoter activity and show that it is very active in a cervix carcinoma cell line. Interestingly, despite hallmarks of a housekeeping gene, we show that the 37 LRP/p40 gene promoter can be down-regulated by two potentially anticancerous cytokines, TNF-alpha and IFN-gamma. In addition, the dual fate of the protein, i.e., being intracellularly involved in the cell translation machinery and incorporated into a 67-kDa cell surface protein functioning as a laminin receptor (67LR), is differentially affected by the treatment. Our data suggest multiple regulation levels in the control of the 67LR/37LRP/p40 molecule expression and uncover new clues for the understanding of both the control of expression of this metastasis-associated molecule and the IFN-gamma and TNF-alpha anticancerous action.

摘要

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