摘要
MN1基因编码转录共激活因子,在某些急性髓系白血病(AML)中高表达。MN1在正常核型AML患者中的高表达与预后差和生存时间短相关;在全部inv(16)AML中高表达,其高表达在非M3的AML中被认为与对维甲酸的耐药有关。本文就MN1基因的结构和作用机制、MN1-TEL与急性髓系白血病,MN1与正常核型AML,MN1与inv(16)AML,MN1与维甲酸耐药等作一综述。
The transcriptional coactivator MN1 has been identified as a gene overexpressed in certain types of human acute myeloid leukemia. Overexpression of this gene is associated with all inv (16) AML, retinoic acid-resistance, a worse prognosis as well as a shorter survival in AML patients with a normal karyotype. This article reviews the role of MN1 in acute myeloid leukemia including MN1 gene structure and action mechnism, MN1-TEL and AML with normal karyotype, MN1 and inv(16) AML, MN1 and retinoic ocid-resistance, and so on.
出处
《中国实验血液学杂志》
CAS
CSCD
2009年第2期504-508,共5页
Journal of Experimental Hematology
基金
江苏省卫生厅医学科研课题(编号H200703)
江苏省六大高峰人才项目资助(编号160IB04)