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miRNA-15 和 miRNA-16 表达替换对慢性淋巴细胞白血病的影响:治疗意义。

Effects of miRNA-15 and miRNA-16 expression replacement in chronic lymphocytic leukemia: implication for therapy.

机构信息

Department Integrated Oncological Therapies, Molecular Pathology Unit, IRCCS-A.O.U., San Martino-IST, Genoa, Italy.

Diagnostic Imaging and Senology, IRCCS-A.O.U., San Martino-IST, Genoa, Italy.

出版信息

Leukemia. 2017 Sep;31(9):1894-1904. doi: 10.1038/leu.2016.394. Epub 2017 Jan 5.

DOI:10.1038/leu.2016.394
PMID:28053325
Abstract

Chronic lymphocytic leukemia (CLL) clones are characterized by loss of a critical region in 13q14.3, (del(13)(q14)) involving the microRNA (miRNA) cluster miR-15a and miR-16-1. We have investigated the effects of replacement of miR-15a and miR-16-1. CLL cells transfected with these miRNA mimics exhibited a decrease in cell viability in vitro and impaired capacity for engraftment and growth in NOD/Shi-scid,γcnull (NSG) mice. No synergistic effects were observed when the two miRNA mimics were combined. The phenomena were not restricted to CLL with the del(13)(q14) lesion. Similar effects induced by miRNA mimics were seen in cells with additional chromosomal abnormalities with the exception of certain CLL clones harboring TP53 alterations. Administration of miRNA mimics to NSG mice previously engrafted with CLL clones resulted in substantial tumor regression. CLL cell transfection with miR-15a and miR-16-1-specific inhibitors resulted in increased cell viability in vitro and in an enhanced capacity of the engrafted cells to grow in NSG mice generating larger splenic nodules. These data demonstrate that the strong control by miR-15a and miR-16-1 on CLL clonal expansion is exerted also at the level of full-blown leukemia and provide indications for a miRNA-based therapeutic strategy.

摘要

慢性淋巴细胞白血病(CLL)克隆的特征是 13q14.3 关键区域缺失,(del(13)(q14))涉及 microRNA(miRNA)簇 miR-15a 和 miR-16-1。我们研究了替代 miR-15a 和 miR-16-1 的效果。转染这些 miRNA 模拟物的 CLL 细胞在体外表现出细胞活力下降,在 NOD/Shi-scid,γcnull(NSG)小鼠中植入和生长能力受损。当两种 miRNA 模拟物结合使用时,没有观察到协同效应。这些现象不仅限于具有 del(13)(q14) 病变的 CLL。除了某些携带 TP53 改变的 CLL 克隆外,具有其他染色体异常的细胞也观察到类似的 miRNA 模拟物诱导的效应。将 miRNA 模拟物施用于先前植入 CLL 克隆的 NSG 小鼠,导致肿瘤明显消退。CLL 细胞转染 miR-15a 和 miR-16-1 特异性抑制剂导致体外细胞活力增加,并增强植入细胞在 NSG 小鼠中生长的能力,生成更大的脾脏结节。这些数据表明,miR-15a 和 miR-16-1 对 CLL 克隆扩增的强烈控制也在完全白血病水平上发挥作用,并为基于 miRNA 的治疗策略提供了依据。

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