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miR-145 在肾细胞癌中作为肿瘤抑制因子发挥作用,靶向两个癌基因,ANGPT2 和 NEDD9。

miR-145 functions as tumor suppressor and targets two oncogenes, ANGPT2 and NEDD9, in renal cell carcinoma.

机构信息

Department of Clinical Laboratory, Peking University Shenzhen Hospital, Shenzhen, 518036, China.

出版信息

J Cancer Res Clin Oncol. 2014 Mar;140(3):387-97. doi: 10.1007/s00432-013-1577-z. Epub 2014 Jan 3.

Abstract

PURPOSE

Abnormal expression of miRNAs is closely related to a variety of human cancers. The purpose of this study is to identify new tumor suppressor miRNA and elucidate its physiological function and mechanism in renal cell carcinoma (RCC).

METHODS

The expression of miR-145 in 45 RCC and adjacent normal tissues was performed by quantitative RT-PCR. Cell proliferation, migration, invasion, apoptosis and cycle assays were carried out for functional analysis after miR-145 transfection. Two target genes of miR-145 were identified by luciferase reporter assay. The altered expression of 84 epithelial to mesenchymal transition (EMT)-related genes after miR-145 transfection was detected by RT(2) Profiler EMT PCR array.

RESULTS

The expression of miR-145 was downregulated in RCC compared to their normal adjacent tissues. Restoring miR-145 expression in RCC cell lines dramatically suppressed cell proliferation, migration and invasion, and induced cell apoptosis and G2-phase arrest. We further validated those miR-145 targets two oncogenes, ANGPT2 and NEDD9 in RCC. In addition, miR-145 was found to regulate numerous genes involved in the EMT.

CONCLUSIONS

These findings demonstrate that miR-145 functions as tumor suppressor in RCC, suggesting that miR-145 may be a potential therapeutic target for RCC.

摘要

目的

miRNA 的异常表达与多种人类癌症密切相关。本研究旨在鉴定新的肿瘤抑制 miRNA,并阐明其在肾细胞癌(RCC)中的生理功能和机制。

方法

通过定量 RT-PCR 检测 miR-145 在 45 例 RCC 及相邻正常组织中的表达。转染 miR-145 后进行细胞增殖、迁移、侵袭、凋亡和周期检测,进行功能分析。通过荧光素酶报告基因检测鉴定 miR-145 的两个靶基因。转染 miR-145 后,通过 RT(2) Profiler EMT PCR 阵列检测 84 个上皮间质转化(EMT)相关基因的表达变化。

结果

与正常相邻组织相比,RCC 中 miR-145 的表达下调。在 RCC 细胞系中恢复 miR-145 表达可显著抑制细胞增殖、迁移和侵袭,并诱导细胞凋亡和 G2 期阻滞。我们进一步验证了 miR-145 在 RCC 中的两个靶基因,ANGPT2 和 NEDD9,这两个基因均为癌基因。此外,miR-145 还被发现调节 EMT 过程中涉及的许多基因。

结论

这些发现表明,miR-145 在 RCC 中作为肿瘤抑制因子发挥作用,提示 miR-145 可能是 RCC 的潜在治疗靶点。

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