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DNA 甲基化与原发性免疫性血小板减少症。

DNA methylation and primary immune thrombocytopenia.

机构信息

State Key Laboratory of Experimental Hematology, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, PR China.

出版信息

Semin Hematol. 2013 Jan;50 Suppl 1:S116-26. doi: 10.1053/j.seminhematol.2013.03.022.

Abstract

DNA methylation is a heritable, stable, and also reversible way of DNA modification; it can regulate gene expression without changing the nucleotide sequences. Because it takes part in regulation of immune responses, the loss of methylation homeostasis in immune cells will result in autoimmune disease by inducing aberrant gene expression. Primary immune thrombocytopenia (ITP) is an acquired autoimmune disease with many immune deficiencies. Recently, it was well documented that abnormal DNA methylation is also involved in the etiology of ITP. In this review, we elucidate the role of DNA methylation in autoimmune diseases by summarizing the DNA methylation-sensitive genes and the relationship between DNA methylation and ITP.

摘要

DNA 甲基化是一种可遗传、稳定且可逆转的 DNA 修饰方式;它可以调节基因表达,而不改变核苷酸序列。由于它参与免疫反应的调节,免疫细胞中甲基化平衡的丧失会通过诱导异常基因表达导致自身免疫性疾病。原发性免疫性血小板减少症 (ITP) 是一种获得性自身免疫性疾病,存在许多免疫缺陷。最近有充分的文献记载表明,异常的 DNA 甲基化也参与了 ITP 的发病机制。在这篇综述中,我们通过总结 DNA 甲基化敏感基因和 DNA 甲基化与 ITP 之间的关系,阐明了 DNA 甲基化在自身免疫性疾病中的作用。

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