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An in vitro system for identifying agents capable of changing serum lipoprotein(a) concentration by regulating the transcriptional activity of the apolipoprotein(a) gene promoter.

作者信息

Azuma H, Yamaguchi H, Mima N, Shirakawa M, Miyamoto K, Kanagawa Y, Watanabe A, Shigekiyo T, Saito S

机构信息

First Department of Internal Medicine, School of Medicine, University of Tokushima, Japan.

出版信息

Biochem Biophys Res Commun. 1996 Oct 14;227(2):570-5. doi: 10.1006/bbrc.1996.1547.

DOI:10.1006/bbrc.1996.1547
PMID:8878554
Abstract

A high serum concentration of lipoprotein(a) [Lp(a)] is a significant and independent risk factor for cardiovascular disease. We examined the effects of agents on the transcriptional activity of the apolipoprotein(a) [apo(a)] gene promoter and determined whether drugs identified by this assay would affect the serum concentration of Lp(a) in vivo. All-trans-retinoic acid (ATRA) and interleukin-6 increased the transcriptional activity of the apo(a) gene promoter 2.1- and 2.5-fold, respectively, whereas danazol reduced activity to 76% of the control value. Triiodothyronine had no effect on transcriptional activity. Treatment of two acute promyelocytic leukemia patients with ATRA induced maximal 2.7- and 3.2-fold increases in serum Lp(a) concentrations, respectively. Thus, the in vitro luciferase assay system is capable of identifying agents that affect the serum concentration of Lp(a) and thus may prove beneficial in the screening of new drugs for treatment of individuals with high serum Lp(a) concentrations.

摘要

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