4.6 Article

The tRNA-Derived Fragment-3017A Promotes Metastasis by Inhibiting NELL2 in Human Gastric Cancer

期刊

FRONTIERS IN ONCOLOGY
卷 10, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fonc.2020.570916

关键词

tRNA-derived fragment; gastric cancer; lymph node metastasis; NELL2; molecular mechanism

类别

资金

  1. Natural Science Foundation of China [81872031]
  2. Major R&D Plan of Liaoning Province [2019JH1/10300007]
  3. Xingliao Talents Program in Liaoning Province [XLYC1807164]
  4. Scientific and technological innovation talents program of Shenyang [RC190202]

向作者/读者索取更多资源

This study found that higher levels of tRF-3017A were associated with significantly higher lymph node metastasis in gastric cancer patients, and tRF-3017A may play a role in promoting the migration and invasion of gastric cancer cells by silencing the tumor suppressor NELL2.
tRNA-derived fragments (tRFs) are a new classification of small non-coding RNAs (sncRNAs) derived from the specific cleavage of precursors and mature tRNAs. Accumulating recent evidence has shown that tRFs are frequently abnormal in several cancers. Nevertheless, the role of tRFs in gastric cancer and its mechanism remain unclear. In this study, we found abnormal expression of tRF-3017A (derived from tRNA-Val-TAC) in gastric cancer tissues and cell lines and confirmed its effect on promoting the invasion and migration of gastric cancer cells through functional experiments in vitro. Analysis of clinicopathologic data showed patients with higher tRF-3017A were associated with significantly higher lymph node metastasis. Mechanistic investigation implies that tRF-3017A regulates the tumor suppressor gene NELL2 through forming the RNA-induced silencing complex (RISC) with Argonaute (AGO) proteins. In this study, we found that higher tRF-3017A were associated with significantly higher lymph node metastasis in gastric cancer patients and the tRF-3017A may play a role in promoting the migration and invasion of gastric cancer cells by silencing tumor suppressor NELL2.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据