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铁吸收、相关疾病及治疗的分子视角

Molecular perspective of iron uptake, related diseases, and treatments.

作者信息

Shokrgozar Negin, Golafshan Habib Allah

机构信息

Diagnostic Laboratory Sciences and Technology Research Center, School of Paramedical Sciences, Shiraz University of Medical Sciences, Shiraz, Iran.

出版信息

Blood Res. 2019 Mar;54(1):10-16. doi: 10.5045/br.2019.54.1.10. Epub 2019 Mar 21.

Abstract

Iron deficiency anemia and anemia of chronic disorders are the most common types of anemia. Disorders of iron metabolism lead to different clinical scenarios such as iron deficiency anemia, iron overload, iron overload with cataract and neurocognitive disorders. Regulation of iron in the body is a complex process and different regulatory proteins are involved in iron absorption and release from macrophages into hematopoietic tissues. Mutation in these regulatory genes is the most important cause of iron refractory iron deficiency anemia (IRIDA). This review provides a glance into the iron regulation process, diseases related to iron metabolism, and appropriate treatments at the molecular level.

摘要

缺铁性贫血和慢性病性贫血是最常见的贫血类型。铁代谢紊乱会导致不同的临床情况,如缺铁性贫血、铁过载、伴有白内障和神经认知障碍的铁过载。体内铁的调节是一个复杂的过程,不同的调节蛋白参与铁从巨噬细胞吸收并释放到造血组织的过程。这些调节基因的突变是难治性缺铁性贫血(IRIDA)的最重要原因。本综述简要介绍了铁调节过程、与铁代谢相关的疾病以及分子水平上的适当治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dd2/6439303/c97cc4a15f7f/br-54-10-g001.jpg

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