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miR-15a/16-1 增强维甲酸诱导的白血病细胞分化,且受维甲酸上调。

miR-15a/16-1 enhances retinoic acid-mediated differentiation of leukemic cells and is up-regulated by retinoic acid.

机构信息

Laboratory of Internal Medicine, The First Affiliated Hospital of Wenzhou Medical College, Wenzhou, Zhejiang, China.

出版信息

Leuk Lymphoma. 2011 Dec;52(12):2365-71. doi: 10.3109/10428194.2011.601476. Epub 2011 Aug 12.

Abstract

miR-15a and miR-16-1 (miR-15a/16-1) have been implicated in apoptosis, cell cycle regulation and chemosensitivity of tumor cells, but little is known about the role of miR-15a/16-1 in the differentiation of leukemic cells. In this study, we found that the expression level of miR-15a/16-1 was up-regulated by all-trans retinoic acid (ATRA) treatment in NB4, HL-60 and U937 cell lines and primary leukemic cells. Overexpression of miR-15a/16-1 could not directly drive cells to undergo differentiation but enhanced ATRA-induced differentiation in NB4 and U937 cells. Up-regulation of miR-15a/16-1 was also observed in 36 patients with acute myeloid leukemia (AML) who achieved a complete remission (CR), and two of them showed sharp down-regulation of miR-15a/16-1 when they had a molecular relapse. These data indicate that miR-15a/16-1 plays an important role in the ATRA-induced differentiation of leukemic and primary AML cells.

摘要

miR-15a 和 miR-16-1(miR-15a/16-1)已被牵涉到细胞凋亡、细胞周期调控和肿瘤细胞的化疗敏感性中,但对于 miR-15a/16-1 在白血病细胞分化中的作用知之甚少。在本研究中,我们发现全反式维甲酸(ATRA)处理可上调 NB4、HL-60 和 U937 细胞系和原代白血病细胞中 miR-15a/16-1 的表达水平。miR-15a/16-1 的过表达不能直接驱动细胞分化,但可增强 ATRA 诱导的 NB4 和 U937 细胞分化。36 例急性髓细胞白血病(AML)患者在达到完全缓解(CR)时也观察到 miR-15a/16-1 的上调,其中 2 例在分子复发时 miR-15a/16-1 急剧下调。这些数据表明 miR-15a/16-1 在 ATRA 诱导的白血病和原代 AML 细胞分化中发挥重要作用。

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