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Sterol regulatory element-binding protein (SREBP)-1: gene regulatory target for insulin resistance?

机译:甾醇调节元件结合蛋白(SREBP)-1:胰岛素抵抗的基因调节靶标?

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摘要

The combined appearance of different cardiovascular risk factors seems to be more prevalent in individuals with decreased insulin sensitivity and increased visceral obesity, thereby being components of the so-called metabolic syndrome. Alterations in transcription factors result in complex dysregulation of gene expression, which might be the key to understanding insulin resistance-associated clinical clustering of coronary risk factors at the cellular or gene regulatory level. Recent examples are peroxisome proliferator-activated receptors and sterol regulatory element-binding proteins (SREBPs), which also appear to be novel drug targets. The authors have recently shown that SREBPs are substrates of mitogen-activated protein kinases, and propose that SREBP-1 might play a role in the development of cellular features belonging to lipotoxicity and, possibly, syndrome X.
机译:胰岛素敏感性降低和内脏肥胖增加的个体中,不同心血管危险因素的综合表现似乎更为普遍,因此是所谓的代谢综合征的组成部分。转录因子的改变导致基因表达的复杂失调,这可能是在细胞或基因调控水平上了解胰岛素抵抗相关冠状动脉危险因素临床聚类的关键。最近的例子是过氧化物酶体增殖物激活的受体和固醇调节元件结合蛋白(SREBPs),它们也似乎是新的药物靶标。作者最近表明,SREBPs是促分裂原活化蛋白激酶的底物,并提出SREBP-1可能在脂毒性和X综合征综合症的细胞特征发展中发挥作用。

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