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Internalization of Exosomes through Receptor-Mediated Endocytosis.外泌体通过受体介导的内吞作用内化。
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Long non-coding RNA NEAT1 shows high expression unrelated to molecular features and clinical outcome in multiple myeloma.长链非编码RNA NEAT1在多发性骨髓瘤中呈现出与分子特征及临床结局无关的高表达。
Haematologica. 2019 Feb;104(2):e72-e76. doi: 10.3324/haematol.2018.201301. Epub 2018 Sep 13.
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Therapeutic vulnerability of multiple myeloma to MIR17PTi, a first-in-class inhibitor of pri-miR-17-92.靶向 pri-miR-17-92 的首创抑制剂 MIR17PTi 对多发性骨髓瘤的治疗易感性
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MALAT1: a druggable long non-coding RNA for targeted anti-cancer approaches.MALAT1:一种可成药的长非编码 RNA,可用于靶向抗癌方法。
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Drugging the lncRNA MALAT1 via LNA gapmeR ASO inhibits gene expression of proteasome subunits and triggers anti-multiple myeloma activity.通过 LNA -gapmeR ASO 对 lncRNA MALAT1 进行药物处理可抑制蛋白酶体亚基的基因表达并引发抗多发性骨髓瘤活性。
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Cancer statistics, 2018.癌症统计数据,2018 年。
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Replenishing exosomes from older bone marrow stromal cells with miR-340 inhibits myeloma-related angiogenesis.用miR-340补充来自老年骨髓基质细胞的外泌体可抑制骨髓瘤相关的血管生成。
Blood Adv. 2017 May 16;1(13):812-823. doi: 10.1182/bloodadvances.2016003251. eCollection 2017 May 23.
8
Inhibition of EZH2 triggers the tumor suppressive miR-29b network in multiple myeloma.EZH2的抑制触发了多发性骨髓瘤中的肿瘤抑制性miR-29b网络。
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Cellular uptake of extracellular vesicles is mediated by clathrin-independent endocytosis and macropinocytosis.细胞对细胞外囊泡的摄取是由网格蛋白非依赖内吞作用和巨胞饮作用介导的。
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循环微RNA及其在多发性骨髓瘤中的作用

Circulating microRNAs and Their Role in Multiple Myeloma.

作者信息

Federico Cinzia, Sacco Antonio, Belotti Angelo, Ribolla Rossella, Cancelli Valeria, Giacomini Arianna, Ronca Roberto, Chiarini Marco, Imberti Luisa, Marini Mirella, Rossi Giuseppe, Presta Marco, Paiva Bruno, Roccaro Aldo M

机构信息

Clinical Research Development and Phase I Unit, ASST Spedali Civili di Brescia, 25123 Brescia, Italy.

CREA Laboratory, ASST Spedali Civili di Brescia, 25123 Brescia, Italy.

出版信息

Noncoding RNA. 2019 May 2;5(2):37. doi: 10.3390/ncrna5020037.

DOI:10.3390/ncrna5020037
PMID:31052608
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6631121/
Abstract

Multiple myeloma (MM) is a plasma cell dyscrasia characterized by bone marrow infiltration of clonal plasma cells. The recent literature has clearly demonstrated clonal heterogeneity in terms of both the genomic and transcriptomic signature of the tumor. Of note, novel studies have also highlighted the importance of the functional cross-talk between the tumor clone and the surrounding bone marrow milieu, as a relevant player of MM pathogenesis. These findings have certainly enhanced our understanding of the underlying mechanisms supporting MM pathogenesis and disease progression. Within the specific field of small non-coding RNA-research, recent studies have provided evidence for considering microRNAs as a crucial regulator of MM biology and, in this context, circulating microRNAs have been shown to potentially contribute to prognostic stratification of MM patients. The present review will summarize the most recent studies within the specific topic of microRNAs and circulating microRNAs in MM.

摘要

多发性骨髓瘤(MM)是一种浆细胞发育异常疾病,其特征为克隆性浆细胞浸润骨髓。最近的文献清楚地表明,在肿瘤的基因组和转录组特征方面存在克隆异质性。值得注意的是,新的研究还强调了肿瘤克隆与周围骨髓微环境之间功能相互作用的重要性,这是MM发病机制的一个相关因素。这些发现无疑加深了我们对支持MM发病机制和疾病进展的潜在机制的理解。在小非编码RNA研究的特定领域,最近的研究提供了证据,表明微小RNA是MM生物学的关键调节因子,在此背景下,循环微小RNA已被证明可能有助于MM患者的预后分层。本综述将总结MM中微小RNA和循环微小RNA这一特定主题的最新研究。