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佛波醇12-肉豆蔻酸酯13-乙酸酯在21MT2乳腺癌中使elafin重新表达是由elafin启动子中的Ap1位点介导的。

Re-expression of elafin in 21MT2 breast carcinomas by phorbol 12-myristate 13-acetate is mediated by the Ap1 site in the elafin promoter.

作者信息

Zhang M, Magit D, Pardee A B, Sager R

机构信息

Dana-Farber Cancer Institute and Harvard Medical School, Boston, Massachusetts 02115, USA.

出版信息

Cancer Res. 1997 Oct 15;57(20):4631-6.

PMID:9377579
Abstract

elafin is a unique elastase inhibitor. It is differentially expressed at the transcriptional level in human normal mammary epithelial cells and carcinomas. The elafin gene is induced by PMA in 21MT2 breast tumor cells. By deletion analysis and mutagenesis, we have identified the Ap1 site in the promoter as the cis element mediating transcriptional activation of elafin in 70N normal breast cells and its induction by phorbol 12-myristate 13-acetate (PMA) in 21MT2 breast tumors. PMA treatment induces AP1 factor expression, which binds to the Ap1 site of the elafin promoter. Mutation of this Ap1 abolishes the capability of induction by PMA. Furthermore, our data provide a basis for therapeutic manipulation of proteinase inhibitors such as elafin.

摘要

弹性蛋白酶抑制因子是一种独特的弹性蛋白酶抑制剂。它在人类正常乳腺上皮细胞和癌组织中在转录水平上差异表达。弹性蛋白酶抑制因子基因在21MT2乳腺肿瘤细胞中被佛波酯(PMA)诱导。通过缺失分析和诱变,我们已确定启动子中的Ap1位点是在70N正常乳腺细胞中介导弹性蛋白酶抑制因子转录激活及其在21MT2乳腺肿瘤中被佛波醇12 - 肉豆蔻酸酯13 - 乙酸酯(PMA)诱导的顺式元件。PMA处理诱导AP1因子表达,该因子与弹性蛋白酶抑制因子启动子的Ap1位点结合。此Ap1位点的突变消除了PMA诱导的能力。此外,我们的数据为诸如弹性蛋白酶抑制因子等蛋白酶抑制剂的治疗性操作提供了依据。

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