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长链非编码 RNA NEF 在三阴性乳腺癌中下调,与预后不良相关。

LncRNA NEF is downregulated in triple negative breast cancer and correlated with poor prognosis.

机构信息

School of Medicine and Life Sciences, University of Jinan-Shandong Academy of Medical Science, Jinan, China.

Department of Oncology, Shandong Academy of Medical Science, Shandong Cancer Hospital Affiliated to Shandong University, Jinan, China.

出版信息

Acta Biochim Biophys Sin (Shanghai). 2019 Apr 1;51(4):386-392. doi: 10.1093/abbs/gmz021.

Abstract

LncRNA NEF has been proved to be a tumor suppressor in liver cancer. In the present study, we found that lncRNA NEF was downregulated and miRNA-155 was upregulated in plasma of triple-negative breast cancer (TNBC) patients compared with those in controls. These two factors were inversely correlated only in TNBC patients but not in controls. Altered expression of lncRNA NEF and miRNA-155 distinguished TNBC patients from healthy controls. Follow-up study showed that low level of lncRNA NEF and high level of miRNA-155 were correlated with poor survival. LncRNA NEF overexpression inhibited the migration and invasion of TNBC cells, while miRNA-155 overexpression promoted the migration and invasion of TNBC cells, but showed no significant effects on cancer cell proliferation. MiRNA-155 overexpression partially rescued the inhibited cell migration and invasion caused by lncRNA NEF overexpression. LncRNA NEF overexpression inhibited miRNA-155 expression, while miRNA-155 overexpression showed no significant effect on lncRNA NEF expression. Therefore, lncRNA NEF may participate in TNBC by negatively regulating miRNA-155.

摘要

长链非编码 RNA NEF 已被证明在肝癌中是一种肿瘤抑制因子。在本研究中,我们发现与对照组相比,三阴性乳腺癌(TNBC)患者的血浆中 lncRNA NEF 下调,miRNA-155 上调。这两个因素仅在 TNBC 患者中呈负相关,而在对照组中则不相关。lncRNA NEF 和 miRNA-155 的表达改变将 TNBC 患者与健康对照区分开来。随访研究表明,lncRNA NEF 水平低和 miRNA-155 水平高与生存不良相关。lncRNA NEF 过表达抑制 TNBC 细胞的迁移和侵袭,而 miRNA-155 过表达促进 TNBC 细胞的迁移和侵袭,但对癌细胞增殖没有显著影响。miRNA-155 过表达部分挽救了 lncRNA NEF 过表达引起的抑制细胞迁移和侵袭。lncRNA NEF 过表达抑制 miRNA-155 的表达,而 miRNA-155 过表达对 lncRNA NEF 的表达没有显著影响。因此,lncRNA NEF 可能通过负调控 miRNA-155 参与 TNBC。

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