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中胚层发育候选基因 1 的新致癌功能及其在膀胱癌细胞系中受 miR-574-3p 的调控。

Novel oncogenic function of mesoderm development candidate 1 and its regulation by MiR-574-3p in bladder cancer cell lines.

机构信息

Department of Urology, Graduate School of Medical and Dental Sciences, Kagoshima University, Kagoshima, Japan.

出版信息

Int J Oncol. 2012 Apr;40(4):951-9. doi: 10.3892/ijo.2011.1294. Epub 2011 Dec 13.

DOI:10.3892/ijo.2011.1294
PMID:22179486
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3584521/
Abstract

Our previous studies suggested that microRNA (miR)-574-3p is a candidate tumor suppressor microRNA (miRNA) in human bladder cancer (BC). Among 17 down-regulated miRNAs, miR-574-3p is located on chromosome 4p14 where we had identified a chromosomal loss region by array-CGH in BC cell lines. MiR-574-3p expression was down-regulated in BC cell lines. Gain-of-function analysis revealed that cell proliferation, migration and invasion were significantly inhibited in miR‑574‑3p-transfected BC cell lines. Flow cytometry analysis showed that cell apoptosis was induced in miR-574-3p transfectants. Oligo microarray analysis suggested that the mesoderm development candidate 1 (MESDC1) gene was a target gene in miR-574-3p transfectants. Luciferase assays revealed that miR‑574‑3p was directly bound to MESDC1 mRNA. MESDC1 is predicted to be a novel actin-binding protein located on chromosome 15q13. Although the gene is conserved among many species, its functional role is still unknown in both human malignancies and normal tissues. Loss-of-function studies demonstrated that cell proliferation, migration and invasion were significantly inhibited in si-MESDC1-transfected BC cell lines. Flow cytometry analysis showed that apoptosis was induced in si-MESDC1 transfectants. We are the first to demonstrate that miR-574-3p is a miRNA with tumor suppressor function and that MESDC1 (which has a potential oncogenic function in BC) may be targeted by miR-574-3p.

摘要

我们之前的研究表明,微小 RNA (miR)-574-3p 是人类膀胱癌 (BC) 的候选肿瘤抑制 miRNA。在 17 个下调的 miRNA 中,miR-574-3p 位于染色体 4p14 上,我们曾通过 array-CGH 在 BC 细胞系中鉴定出一个染色体缺失区域。miR-574-3p 在 BC 细胞系中表达下调。功能获得分析显示,miR-574-3p 转染的 BC 细胞系的细胞增殖、迁移和侵袭显著受到抑制。流式细胞术分析显示,miR-574-3p 转染物诱导细胞凋亡。寡核苷酸微阵列分析表明,中胚层发育候选基因 1 (MESDC1) 基因是 miR-574-3p 转染物的靶基因。荧光素酶报告基因实验显示 miR-574-3p 直接与 MESDC1 mRNA 结合。MESDC1 被预测为一种位于染色体 15q13 上的新型肌动蛋白结合蛋白。尽管该基因在许多物种中都保守,但在人类恶性肿瘤和正常组织中,其功能作用仍不清楚。功能丧失研究表明,si-MESDC1 转染的 BC 细胞系的细胞增殖、迁移和侵袭显著受到抑制。流式细胞术分析显示,si-MESDC1 转染物诱导细胞凋亡。我们是第一个证明 miR-574-3p 是具有肿瘤抑制功能的 miRNA,并且 MESDC1(在 BC 中具有潜在的致癌功能)可能是 miR-574-3p 的靶基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/789e/3584521/9a29be6b163e/IJO-40-04-0951-g04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/789e/3584521/09e53db23f96/IJO-40-04-0951-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/789e/3584521/2ef86fbc7c2c/IJO-40-04-0951-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/789e/3584521/1bc2a30d1028/IJO-40-04-0951-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/789e/3584521/9a29be6b163e/IJO-40-04-0951-g04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/789e/3584521/09e53db23f96/IJO-40-04-0951-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/789e/3584521/2ef86fbc7c2c/IJO-40-04-0951-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/789e/3584521/1bc2a30d1028/IJO-40-04-0951-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/789e/3584521/9a29be6b163e/IJO-40-04-0951-g04.jpg

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