Novel targets in the treatment of neuroendocrine tumors: RBP2

E. Maggi, J. Crabtree
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引用次数: 1

Abstract

Retinoblastoma binding protein 2, also known as RBP2, JARID1A or KDM5A, is an H3K4 demethylase implicated in a variety of non-neuroendocrine, and more recently, neuroendocrine tumors (NETs). NETs are tumors that form from neuroendocrine cells in tissues of the GI tract, endocrine pancreas, lung, skin and other tissues. RBP2 is expressed at abnormally high levels in NETs and recent work demonstrates that modulation of RBP2 in vitro and in vivo impacts end points of tumorigenesis. Interestingly, the demethylase activity of RBP2 is not exclusively responsible for these changes, as RBP2's binding partners may mediate its activity in a tissue- or context-dependent manner. Here, we discuss the features of RBP2 and its role in cell cycle regulation, angiogenesis and drug resistance in cancer.
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治疗神经内分泌肿瘤的新靶点:RBP2
视网膜母细胞瘤结合蛋白2,也被称为RBP2、JARID1A或KDM5A,是一种H3K4去甲基化酶,与多种非神经内分泌和最近的神经内分泌肿瘤(NETs)有关。NETs是由胃肠道、内分泌胰腺、肺、皮肤等组织中的神经内分泌细胞形成的肿瘤。在NETs中,RBP2的表达水平异常高,最近的研究表明,体外和体内对RBP2的调节会影响肿瘤发生的终点。有趣的是,RBP2的去甲基酶活性并不是这些变化的唯一原因,因为RBP2的结合伙伴可能以组织或环境依赖的方式调节其活性。在此,我们讨论了RBP2的特点及其在肿瘤细胞周期调节、血管生成和耐药中的作用。
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来源期刊
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审稿时长
13 weeks
期刊介绍: International Journal of Endocrine Oncology is a quarterly, peer-reviewed journal that helps the clinician to keep up to date with best practice in this fast-moving field. The journal highlights significant advances in basic and translational research, and places them in context for future therapy. The journal presents the latest research findings in diagnosis and management of endocrine cancer, together with authoritative reviews, cutting-edge editorials and perspectives that highlight hot topics and controversy in the field. Independent drug evaluations assess newly approved medications and their role in clinical practice. The journal welcomes the unsolicited submission of article proposals and original research manuscripts.
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