首页> 外文期刊>FEBS letters. >Thioredoxin stimulates MMP-9 expression, de-regulates the MMP-9/TIMP-1 equilibrium and promotes MMP-9 dependent invasion in human MDA-MB-231 breast cancer cells.
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Thioredoxin stimulates MMP-9 expression, de-regulates the MMP-9/TIMP-1 equilibrium and promotes MMP-9 dependent invasion in human MDA-MB-231 breast cancer cells.

机译:硫氧还蛋白刺激人MDA-MB-231乳腺癌细胞中MMP-9的表达,失调MMP-9 / TIMP-1平衡并促进MMP-9依赖性侵袭。

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摘要

Increased expression of thioredoxin (Trx)-1 and matrix metalloproteinase (MMP)-9 associates with malignant breast cancer progression. Here, we describe a functional relationship between Trx-1 and MMP-9 in promoting MDA-MB-231 breast cancer cell invasive behaviour. Trx-1 overexpression stimulated MMP-9 expression, de-regulated the MMP-9/TIMP-1 equilibrium and augmented MMP-9 involvement in a more invasive phenotype. Trx-1 augmented MMP-9 transcription through NF-kappaB, AP-1 and SP1 elements; stimulated p50/p65 NF-kappaB activity and recruitment to the MMP-9 promoter; and facilitated MMP-9 promoter-accessibility to NF-kappaB by preventing HDAC recruitment and maintaining MMP-9 promoter histone acetylation. Our data provide a functional basis for Trx-1 and MMP-9 association in malignant breast cancer and identify Trx-1 and NF-kappaB as potentially druggable targets for reducing MMP-9 involvement in malignant behaviour.
机译:硫氧还蛋白(Trx)-1和基质金属蛋白酶(MMP)-9的表达增加与恶性乳腺癌的进展有关。在这里,我们描述Trx-1和MMP-9在促进MDA-MB-231乳腺癌细胞侵袭行为中的功能关系。 Trx-1的过表达刺激了MMP-9的表达,放松了MMP-9 / TIMP-1的平衡,并增加了MMP-9参与更具侵害性的表型。 Trx-1通过NF-κB,AP-1和SP1元件增强MMP-9转录;刺激p50 / p65NF-κB活性并募集到MMP-9启动子;并通过阻止HDAC募集并维持MMP-9启动子组蛋白乙酰化,促进MMP-9启动子可接近NF-κB。我们的数据为恶性乳腺癌中Trx-1和MMP-9的结合提供了功能基础,并确定Trx-1和NF-kappaB是减少MMP-9参与恶性行为的潜在药物靶点。

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