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AHI-1:一种新型信号蛋白,是人类白血病和脑部疾病的潜在治疗靶点。

AHI-1: a novel signaling protein and potential therapeutic target in human leukemia and brain disorders.

作者信息

Esmailzadeh Sharmin, Jiang Xiaoyan

机构信息

Terry Fox Laboratory, British Columbia Cancer Agency and Department of Medical Genetics, University of British Columbia, Vancouver, BC, Canada.

出版信息

Oncotarget. 2011 Dec;2(12):918-34. doi: 10.18632/oncotarget.405.

Abstract

Progress in the understanding of the molecular and cellular mechanisms of human cancer, including human leukemia and lymphomas, has been spurred by cloning of fusion genes created by chromosomal translocations or by retroviral insertional mutagenesis; a number of oncogenes and tumor suppressors involved in development of a number of malignancies have been identified in this manner. The BCR-ABL fusion gene, originating in a multipotent hematopoietic stem cell, is the molecular signature of chronic myeloid leukemia (CML). Discovery of this fusion gene has led to the development of one of the first successful targeted molecular therapies for cancer (Imatinib). It illustrates the advances that can result from an understanding of the molecular basis of disease. However, there still remain many as yet unidentified mutations that may influence the initiation or progression of human diseases. Thus, identification and characterization of the mechanism of action of genes that contribute to human diseases is an important and opportune area of current research. One promising candidate as a potential therapeutic target is Abelson helper integration site-1(Ahi-1/AHI-1) that was identified by retroviral insertional mutagenesis in murine models of leukemia/lymphomas and is highly elevated in certain human lymphoma and leukemia stem/progenitor cells. It encodes a unique protein with a SH3 domain, multiple SH3 binding sites and a WD40-repeat domain, suggesting that the normal protein has novel signaling activities. A new AHI-1-BCR-ABL-JAK2 interaction complex has recently been identified and this complex regulates transforming activities and drug resistance in CML stem/progenitor cells. Importantly, AHI-1 has recently been identified as a susceptibility gene involved in a number of brain disorders, including Joubert syndrome. Therefore, understanding molecular functions of the AHI-1 gene could lead to important and novel insights into disease processes involved in specific types of diseases. Ultimately, this knowledge will set the stage for translation into new and more effective diagnostic and treatment strategies.

摘要

对人类癌症(包括人类白血病和淋巴瘤)分子和细胞机制的理解取得了进展,这得益于对由染色体易位或逆转录病毒插入诱变产生的融合基因的克隆;通过这种方式,已经鉴定出许多与多种恶性肿瘤发生发展相关的癌基因和肿瘤抑制基因。起源于多能造血干细胞的BCR-ABL融合基因是慢性髓性白血病(CML)的分子标志。这一融合基因的发现促成了首批成功的癌症靶向分子疗法之一(伊马替尼)的开发。它说明了基于对疾病分子基础的理解所能带来的进展。然而,仍有许多尚未鉴定的突变可能影响人类疾病的发生或进展。因此,鉴定和表征导致人类疾病的基因的作用机制是当前研究的一个重要且适时的领域。作为潜在治疗靶点的一个有前景的候选基因是Abelson辅助整合位点1(Ahi-1/AHI-1),它是在白血病/淋巴瘤小鼠模型中通过逆转录病毒插入诱变鉴定出来的,并且在某些人类淋巴瘤和白血病干细胞/祖细胞中高度表达。它编码一种具有SH3结构域、多个SH3结合位点和一个WD40重复结构域的独特蛋白质,这表明正常蛋白质具有新的信号传导活性。最近鉴定出了一种新的AHI-1-BCR-ABL-JAK2相互作用复合物,该复合物调节CML干细胞/祖细胞的转化活性和耐药性。重要的是,AHI-1最近被鉴定为涉及多种脑部疾病(包括Joubert综合征)的易感基因。因此,了解AHI-1基因的分子功能可能会为特定类型疾病所涉及的疾病过程带来重要且新颖的见解。最终,这些知识将为转化为新的、更有效的诊断和治疗策略奠定基础。

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