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miR-187-5p Regulates Cell Growth and Apoptosis in Acute Lymphoblastic Leukemia via DKK2

机译:miR-187-5p通过DKK2调节急性淋巴细胞白血病中的细胞生长和凋亡。

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Acute lymphoblastic leukemia (ALL) is the most common childhood malignancy and causes a high rate of mortality in affected adults. Many subtypes of ALL exist with disruptions in distinct genetic pathways, including those regulated by miRNAs. Here we identify miR-187-5p as being highly upregulated in B-cell ALL and a driver of cellular proliferation and suppressor of apoptosis. We show that miR-187-5p directly targets the 3'-UTR of DKK2 to mediate these effects. We further determine that inhibition of DKK2 by miR-187-5p in Nalm-6 B cells leads to inappropriate activation of Wnt/beta-catenin signaling. Together, these findings reveal that the miR-187-5p DKK2 pathway regulates Wnt/beta-catenin signaling, cell growth, and apoptosis. Our findings provide the first evidence of a role for miR-187-5p in promotion of B-cell ALL.
机译:急性淋巴细胞白血病(ALL)是儿童中最常见的恶性肿瘤,在受影响的成年人中导致很高的死亡率。 ALL的许多亚型都存在独特的遗传途径破坏,包括那些受miRNA调控的途径。在这里,我们确定miR-187-5p在B细胞ALL中是高度上调的,并且是细胞增殖和凋亡抑制的驱动器。我们显示miR-187-5p直接靶向DKK2的3'-UTR以介导这些作用。我们进一步确定,Nalm-6 B细胞中miR-187-5p对DKK2的抑制会导致Wnt /β-catenin信号的不适当激活。总之,这些发现揭示了miR-187-5p DKK2途径调节Wnt /β-catenin信号传导,细胞生长和凋亡。我们的发现为miR-187-5p在促进B细胞ALL中的作用提供了第一个证据。

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