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p38丝裂原活化蛋白激酶通路作为炎症性疾病的治疗靶点。

The p38 MAP kinase pathway as a therapeutic target in inflammatory disease.

作者信息

Saklatvala Jeremy

机构信息

Kennedy Institute of Rheumatology, Imperial College Faculty of Medicine, 1 Aspenlea Road, London W6 8LH, UK.

出版信息

Curr Opin Pharmacol. 2004 Aug;4(4):372-7. doi: 10.1016/j.coph.2004.03.009.

Abstract

The p38 MAPK signalling pathway plays an important role in inflammation and other physiological processes. Specific inhibitors of p38 alpha and beta MAPK block production of the major inflammatory cytokines (i.e. tumour necrosis factor-alpha and interleukin-1) and other proteins (e.g. cyclooxygenase-2), and are anti-inflammatory in animal models of disease. A major function of the pathway is post-transcriptional control of inflammatory gene expression. Many of the mRNAs are unstable (or untranslatable) because of AU-rich elements in the 3'untranslated region. Signalling in the p38 pathway counteracts these and stabilizes the mRNAs by preventing their otherwise rapid de-adenylation.

摘要

p38丝裂原活化蛋白激酶(MAPK)信号通路在炎症和其他生理过程中发挥着重要作用。p38α和β MAPK的特异性抑制剂可阻断主要炎性细胞因子(即肿瘤坏死因子-α和白细胞介素-1)及其他蛋白质(如环氧合酶-2)的产生,并且在疾病动物模型中具有抗炎作用。该信号通路的一个主要功能是对炎症基因表达进行转录后调控。由于3'非翻译区存在富含AU的元件,许多mRNA不稳定(或不可翻译)。p38信号通路中的信号传导可抵消这些作用,并通过防止mRNA快速去腺苷酸化来使其稳定。

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