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miR-3648/FRAT1-FRAT2/c-Myc 负反馈环调节胃癌细胞的转移和侵袭。

The miR-3648/FRAT1-FRAT2/c-Myc negative feedback loop modulates the metastasis and invasion of gastric cancer cells.

机构信息

Guangdong Provincial Key Laboratory of Gastroenterology, Department of Gastroenterology, Nanfang Hospital, Southern Medical University, Guangzhou, 510515, China.

Department of Hematology and Oncology, International Cancer Center, Shenzhen University General Hospital, Xueyuan AVE 1098, Nanshan District, Shenzhen, Guangdong, 518000, P. R. China.

出版信息

Oncogene. 2022 Oct;41(43):4823-4838. doi: 10.1038/s41388-022-02451-2. Epub 2022 Sep 24.

DOI:10.1038/s41388-022-02451-2
PMID:36153370
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9586869/
Abstract

Although the abnormal expression of miRNAs in cancer cells is a widely accepted phenomenon, the molecular mechanisms underlying miR-3648 progression and metastasis in gastric cancer (GC) remain unclear. miR-3648 expression is downregulated and its ectopic expression in GC cells significantly suppressed cell proliferation and metastasis. Mechanistic analyses indicated that miR-3648 directly targets FRAT1 or FRAT2 and inhibits FRAT1- or FRAT2-mediated invasion and motility in vitro and in vivo. Moreover, FRAT1 physically interacted with FRAT2. Furthermore, FRAT1 overexpression promoted GC cell invasion, whereas siRNA-mediated repression of FRAT2 in FRAT1-overexpressing GC cells reversed its invasive potential. Besides, miR-3648 inactivated the Wnt/β-catenin signalling pathway by downregulating FRAT1 and FRAT2 in GC. Interestingly, c-Myc, a downstream effector of Wnt/β-catenin signalling, was also downregulated by miR-3648 overexpression. In turn, c-Myc negatively regulated miR-3648 expression by binding to the miR-3648 promoter. In addition, miR-3648 expression levels were negatively correlated with c-Myc, FRAT1, and FRAT2 expression in fresh gastric samples. Our studies suggest that miR-3648 acts as a tumour-suppressive miRNA and that the miR-3648/FRAT1-FRAT2/c-Myc negative feedback loop could be a critical regulator of GC progression.

摘要

尽管癌细胞中 miRNAs 的异常表达是一个被广泛接受的现象,但 miR-3648 在胃癌(GC)中的进展和转移的分子机制仍不清楚。miR-3648 的表达下调,其在 GC 细胞中的异位表达显著抑制了细胞增殖和转移。机制分析表明,miR-3648 直接靶向 FRAT1 或 FRAT2,并抑制 FRAT1 或 FRAT2 介导的体外和体内侵袭和迁移。此外,FRAT1 与 FRAT2 物理相互作用。此外,FRAT1 的过表达促进了 GC 细胞的侵袭,而在 FRAT1 过表达的 GC 细胞中,siRNA 介导的 FRAT2 抑制逆转了其侵袭潜能。此外,miR-3648 通过下调 FRAT1 和 FRAT2 使 Wnt/β-catenin 信号通路失活。有趣的是,Wnt/β-catenin 信号的下游效应子 c-Myc 也被 miR-3648 过表达下调。反过来,c-Myc 通过结合 miR-3648 启动子负调控 miR-3648 的表达。此外,在新鲜胃样本中,miR-3648 的表达水平与 c-Myc、FRAT1 和 FRAT2 的表达呈负相关。我们的研究表明,miR-3648 作为一种肿瘤抑制 miRNA,miR-3648/FRAT1-FRAT2/c-Myc 负反馈回路可能是 GC 进展的关键调节因子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7972/9586869/2ce7ebe26633/41388_2022_2451_Fig8_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7972/9586869/7b3d6a22dbdf/41388_2022_2451_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7972/9586869/e22331fd22d1/41388_2022_2451_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7972/9586869/9a84a5ed403e/41388_2022_2451_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7972/9586869/2ce7ebe26633/41388_2022_2451_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7972/9586869/5ebeaef6a1e1/41388_2022_2451_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7972/9586869/815238506fb6/41388_2022_2451_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7972/9586869/8cb548bb25e5/41388_2022_2451_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7972/9586869/b1310060a088/41388_2022_2451_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7972/9586869/7b3d6a22dbdf/41388_2022_2451_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7972/9586869/e22331fd22d1/41388_2022_2451_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7972/9586869/9a84a5ed403e/41388_2022_2451_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7972/9586869/2ce7ebe26633/41388_2022_2451_Fig8_HTML.jpg

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