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铁转运与代谢新见解的临床相关性。

The clinical relevance of new insights in iron transport and metabolism.

作者信息

Brissot Pierre, Troadec Marie-Bérengère, Loréal Olivier

机构信息

Service des Maladies du Foie and INSERM U-522, University Hospital Pontchaillou, 35033 Rennes, France.

出版信息

Curr Hematol Rep. 2004 Mar;3(2):107-15.

Abstract

There have been major basic advances in the field of iron metabolism in recent years. These advances include the discoveries of the HFE-1 gene, a series of transmembrane iron transporters or cotransporters (eg, divalent metal transporter-1, duodenal cytochrome b, ferroportin-1, hephaestin, and transferrin receptor-2), and two key regulatory proteins named hepcidin and hemojuvelin. Several mutations of these various proteins have been linked to human diseases. These discoveries have led to major improvements in our understanding of iron physiology and have also profoundly modified and extended the pathologic iron field. Clinical applications have rapidly emerged with the appearance of new iron overload syndromes and the practical input of new genetic tools enabling the noninvasive diagnosis of HFE-1 hemochromatosis. These basic advances are paving the road for innovative therapeutic strategies not only in iron overload syndromes but also in the wide area of chronic disease-related anemia.

摘要

近年来,铁代谢领域取得了重大的基础进展。这些进展包括HFE-1基因、一系列跨膜铁转运蛋白或共转运蛋白(如二价金属转运蛋白-1、十二指肠细胞色素b、铁转运蛋白-1、血浆铜蓝蛋白和转铁蛋白受体-2)的发现,以及两种关键的调节蛋白——铁调素和血色素沉着抑制因子的发现。这些不同蛋白质的几种突变已与人类疾病相关联。这些发现极大地增进了我们对铁生理学的理解,也深刻地改变和扩展了病理性铁领域。随着新的铁过载综合征的出现以及新的基因检测工具的实际应用,使得HFE-1血色素沉着症的无创诊断成为可能,临床应用迅速涌现。这些基础进展不仅为铁过载综合征,也为广泛的慢性病相关性贫血领域的创新治疗策略铺平了道路。

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