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PAPA 综合征的临床、分子和遗传学特征:综述。

Clinical, Molecular, and Genetic Characteristics of PAPA Syndrome: A Review.

机构信息

Sarah M. and Charles E. Seay Center for Musculoskeletal Research, Scottish Rite Hospital for Children, Dallas, Texas 75219.

出版信息

Curr Genomics. 2010 Nov;11(7):519-27. doi: 10.2174/138920210793175921.

Abstract

PAPA syndrome (Pyogenic Arthritis, Pyoderma gangrenosum, and Acne) is an autosomal dominant, hereditary auto-inflammatory disease arising from mutations in the PSTPIP1/CD2BP1 gene on chromosome 15q. These mutations produce a hyper-phosphorylated PSTPIP1 protein and alter its participation in activation of the "inflammasome" involved in interleukin-1 (IL-1β) production. Overproduction of IL-1β is a clear molecular feature of PAPA syndrome. Ongoing research is implicating other biochemical pathways that may be relevant to the distinct pyogenic inflammation of the skin and joints characteristic of this disease. This review summarizes the recent and rapidly accumulating knowledge on these molecular aspects of PAPA syndrome and related disorders.

摘要

PAPA 综合征(化脓性关节炎、坏疽性脓皮病和痤疮)是一种常染色体显性遗传的自身炎症性疾病,由 15q 染色体上 PSTPIP1/CD2BP1 基因的突变引起。这些突变产生了一种过度磷酸化的 PSTPIP1 蛋白,并改变了其参与白细胞介素-1(IL-1β)产生的“炎症小体”激活的过程。白细胞介素-1β的过度产生是 PAPA 综合征的一个明显的分子特征。正在进行的研究表明,其他生化途径可能与该病特征性的皮肤和关节化脓性炎症有关。本综述总结了关于 PAPA 综合征和相关疾病的这些分子方面的最新且快速积累的知识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5694/3048314/53641a6ba396/CG-11-519_F1.jpg

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