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蛋白磷酸酶1抑制剂KEPI在乳腺癌细胞系和组织中的表达下调,并通过MEK-ERK途径参与肿瘤抑制因子EGR1的调节。

Expression of the protein phosphatase 1 inhibitor KEPI is downregulated in breast cancer cell lines and tissues and involved in the regulation of the tumor suppressor EGR1 via the MEK-ERK pathway.

作者信息

Wenzel Katrin, Daskalow Katjana, Herse Florian, Seitz Susanne, Zacharias Ute, Schenk Jörg A, Schulz Herbert, Hubner Norbert, Micheel Burkhard, Schlag Peter M, Osterziel Karl J, Ozcelik Cemil, Scherneck Siegfried, Jandrig Burkhard

机构信息

Max Delbrück Center for Molecular Medicine, Robert-Rössle-Strasse 10, Berlin, Germany.

出版信息

Biol Chem. 2007 May;388(5):489-95. doi: 10.1515/BC.2007.062.

Abstract

KEPI is a protein kinase C-potentiated inhibitory protein for type 1 Ser/Thr protein phosphatases. We found no or reduced expression of KEPI in breast cancer cell lines, breast tumors and metastases in comparison to normal breast cell lines and tissues, respectively. KEPI protein expression and ubiquitous localization was detected with a newly generated antibody. Ectopic KEPI expression in MCF7 breast cancer cells induced differential expression of 95 genes, including the up-regulation of the tumor suppressors EGR1 (early growth response 1) and PTEN (phosphatase and tensin homolog), which is regulated by EGR1. We further show that the up-regulation of EGR1 in MCF7/KEPI cells is mediated by MEK-ERK signaling. The inhibition of this pathway by the MEK inhibitor UO126 led to a strong decrease in EGR1 expression in MCF7/KEPI cells. These results reveal a novel role for KEPI in the regulation of the tumor suppressor gene EGR1 via activation of the MEK-ERK MAPK pathway.

摘要

KEPI是一种针对1型丝氨酸/苏氨酸蛋白磷酸酶的蛋白激酶C增强抑制蛋白。我们发现,与正常乳腺细胞系和组织相比,KEPI在乳腺癌细胞系、乳腺肿瘤及转移灶中的表达分别缺失或降低。使用新制备的抗体检测到了KEPI蛋白的表达及广泛定位。MCF7乳腺癌细胞中KEPI的异位表达诱导了95个基因的差异表达,包括肿瘤抑制因子EGR1(早期生长反应因子1)和PTEN(磷酸酶和张力蛋白同源物)的上调,而PTEN受EGR1调控。我们进一步表明,MCF7/KEPI细胞中EGR1的上调是由MEK-ERK信号传导介导的。MEK抑制剂UO126对该通路的抑制导致MCF7/KEPI细胞中EGR1表达大幅下降。这些结果揭示了KEPI通过激活MEK-ERK MAPK通路在调控肿瘤抑制基因EGR1方面的新作用。

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