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白血病细胞中作为竞争性内源RNA发挥作用的尿激酶型纤溶酶原激活物受体(uPAR)变体的鉴定

Identification of uPAR Variants Acting as ceRNAs in Leukaemia Cells.

作者信息

Alfieri Mariaevelina, Li Santi Anna, Meo Luigia, Giudice Valentina, Selleri Carmine, Ragno Pia

机构信息

Department of Chemistry and Biology, University of Salerno, Via Giovanni Paolo II, 132, 84084 Salerno, Italy.

Clinical Pathology, Pausilipon Hospital, A.O.R.N Santobono-Pausilipon, 80129 Naples, Italy.

出版信息

Cancers (Basel). 2022 Apr 14;14(8):1980. doi: 10.3390/cancers14081980.

Abstract

The 3'untranslated region (3'UTR) of the urokinase (uPA) receptor (uPAR) mRNA can act as a competitive endogenous RNA (ceRNA) in acute myeloid leukaemia (AML) cells, promoting the expression of pro-tumoral targets, including uPAR. Here, we identified three variants of uPAR mRNA containing the 3'UTR, in KG1 and U937 leukaemia cells expressing low and high uPAR levels, respectively. Identified variants lack exon 5 (uPAR Δ5) or exon 6 (uPAR Δ6) or part of exon 6, exon 7 and part of 3'UTR (uPAR Δ6/7). uPAR Δ5 and uPAR Δ6 transcript levels were higher in U937 cells compared to KG1 cells. Both uPAR variants were expressed also in AML blasts, at higher levels as compared to CD34 hematopoietic cells from healthy donors. The presence of the 3'UTR conferred high instability to the uPAR Δ5 variant transcript, preventing its translation in protein. Overexpression of the uPAR Δ5-3'UTR variant regulated the expression of some pro-tumoral factors previously reported to be regulated by the 3'UTR of uPAR and increased KG1 cell adhesion, migration and proliferation. These results demonstrate the expression of uPAR mRNA variants containing the 3'UTR in AML cells and the ceRNA activity and the biological effects of the uPAR Δ5-3'UTR variant.

摘要

尿激酶型纤溶酶原激活物(uPA)受体(uPAR)mRNA的3'非翻译区(3'UTR)在急性髓系白血病(AML)细胞中可作为竞争性内源RNA(ceRNA),促进包括uPAR在内的促肿瘤靶点的表达。在此,我们在分别表达低水平和高水平uPAR的KG1和U937白血病细胞中鉴定出三种含有3'UTR的uPAR mRNA变体。鉴定出的变体缺失外显子5(uPAR Δ5)或外显子6(uPAR Δ6)或外显子6的一部分、外显子7和3'UTR的一部分(uPAR Δ6/7)。与KG1细胞相比,U937细胞中uPAR Δ5和uPAR Δ6的转录水平更高。两种uPAR变体在AML原始细胞中也有表达,与健康供体的CD34造血细胞相比表达水平更高。3'UTR的存在使uPAR Δ5变体转录本具有高度不稳定性,阻止其翻译成蛋白质。uPAR Δ5-3'UTR变体的过表达调节了一些先前报道受uPAR 3'UTR调控的促肿瘤因子的表达,并增加了KG1细胞的黏附、迁移和增殖。这些结果证明了含有3'UTR的uPAR mRNA变体在AML细胞中的表达以及uPAR Δ5-3'UTR变体的ceRNA活性和生物学效应。

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