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Immunomodulation of hematological malignancies using oligonucleotides based-nanomedicines

机译:使用基于寡核苷酸的纳米药物对血液恶性肿瘤的免疫调节

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Hematological malignancies are a group of diseases characterized by clonal proliferation of blood-forming cells. Malignant blood cells are classified as myeloid or lymphoid cells depending on their stem cell origin. Lymphoid malignancies are characterized by lymphocyte accumulation in the blood stream, in the bone marrow, or in lymphatic nodes and organs. Several of these diseases are associated with chromosomal translocations, which cause gene fusion and amplification of expression, while others are characterized with aberrant expression of oncogenes. Overall, these genes play a major role in development and maintenance of malignant clones. The discovery of antisense oligonucleotides and RNA interference (RNAi) mechanisms offer new tools to specifically manipulate gene expression. Systemic delivery of inhibitory oligonucleotides molecules for manipulation of gene expression in lymphocytes holds a great potential for facilitating the development of an oligonucleotides -based therapy platform for lymphoid blood cancer. However, lymphocytes are among the most difficult targets for oligonucleotides delivery, as they are resistant to conventional transfection reagents and are dispersed throughout the body, making it difficult to successfully localize or deliver oligonucleotides payloads via systemic administration. In this review, we will survey the latest progress in the field of oligonucleotides based nanomedicine in the heterogeneous group of hematological malignancies with special emphasis on RNA based strategies. We will describe the most advanced non-viral nanocarriers for RNA delivery to malignant blood cells. We will also discuss targeted strategies for cell specific delivery of RNA molecules using nanoparticles and the therapeutic benefit of manipulating gene function in hematological malignancies. Finally, we will focus on the ex vivo, in vivo, and clinical trial strategies, that are currently under development in hematological malignancies -strategies that might increase the arsenal of drugs available to hematologists in the upcoming years. (C) 2016 Elsevier B.V. All rights reserved.
机译:血液系统恶性肿瘤是一组以造血细胞的克隆增殖为特征的疾病。恶性血细胞根据其干细胞来源分为髓样或淋巴样细胞。淋巴恶性肿瘤的特征是淋巴细胞在血流,骨髓或淋巴结和器官中蓄积。这些疾病中有几种与染色体易位有关,导致基因融合和表达扩增,而另一些则以癌基因的异常表达为特征。总体而言,这些基因在恶性克隆的发展和维持中起着重要作用。反义寡核苷酸和RNA干扰(RNAi)机制的发现为特异性操纵基因表达提供了新工具。用于操纵淋巴细胞中的基因表达的抑制性寡核苷酸分子的系统递送在促进开发基于寡核苷酸的淋巴癌的治疗平台方面具有巨大潜力。然而,淋巴细胞是寡核苷酸递送最困难的靶标之一,因为它们对常规的转染试剂具有抗性并且分散在全身,这使得难以通过全身给药成功地定位或递送寡核苷酸有效载荷。在这篇综述中,我们将调查异源性血液恶性肿瘤组中基于寡核苷酸的纳米医学领域的最新进展,特别强调基于RNA的策略。我们将描述将RNA输送至恶性血细胞的最先进的非病毒纳米载体。我们还将讨论使用纳米颗粒对RNA分子进行细胞特异性递送的靶向策略,以及在血液系统恶性肿瘤中操纵基因功能的治疗益处。最后,我们将专注于血液恶性肿瘤目前正在开发的离体,体内和临床试验策略,这些策略可能会在未来几年增加血液学家对药物的使用。 (C)2016 Elsevier B.V.保留所有权利。

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