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利用胞内抗体对缺氧诱导因子-1进行条件性失活。

Conditional inactivation of HIF-1 using intrabodies.

作者信息

Groot Arjan J, Gort Eelke H, van der Wall Elsken, van Diest Paul J, Vooijs Marc

机构信息

Department of Pathology, University Medical Center Utrecht, 3508 GA, Utrecht, The Netherlands.

出版信息

Cell Oncol. 2008;30(5):397-409. doi: 10.3233/clo-2008-0442.

DOI:10.3233/clo-2008-0442
PMID:18791271
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4618431/
Abstract

Hypoxia is a hallmark of solid cancers and triggers the transcription of genes responsible for cell survival. The transcription factor Hypoxia-Inducible Factor 1 (HIF-1) is a key regulator in this response and frequently activated in human cancer. HIF-1 activation is associated with tumor aggressiveness and poor clinical outcome and, therefore, may provide an attractive therapeutic target. Here we provide a novel approach for HIF-1 targeted therapy using single-domain llama antibodies directed against the HIF-1alpha oxygen dependent degradation domain which encompass the N-terminal transactivation domain. Conditional expression of HIF intrabodies in mammalian cells interfered with binding to pVHL and inhibited hypoxia induced activation of endogenous target genes. Inducible intrabody targeting is a highly specific strategy for temporal protein inactivation and may have applications for disease treatment.

摘要

缺氧是实体癌的一个标志,并触发负责细胞存活的基因转录。转录因子缺氧诱导因子1(HIF-1)是这一反应中的关键调节因子,在人类癌症中经常被激活。HIF-1的激活与肿瘤侵袭性和不良临床结果相关,因此可能是一个有吸引力的治疗靶点。在这里,我们提供了一种针对HIF-1的靶向治疗新方法,使用针对HIF-1α氧依赖性降解结构域的单域骆驼抗体,该结构域包含N端反式激活结构域。HIF胞内抗体在哺乳动物细胞中的条件性表达干扰了与pVHL的结合,并抑制了缺氧诱导的内源性靶基因激活。可诱导的胞内抗体靶向是一种用于暂时蛋白质失活的高度特异性策略,可能在疾病治疗中具有应用价值。