转移
乳腺癌
癌症研究
生物
癌症
细胞生长
竞争性内源性RNA
小RNA
核糖核酸
长非编码RNA
基因
遗传学
作者
Xiaojia Huang,Weige Tan,Ziteng Liu,Xiaoyan Fu,Zongyan Li,Shengqing Lai,Qian Li,Xiaofang Zhong,Fanli Qu,Huayao Zhang,Haiyan Li
出处
期刊:Life Sciences
[Elsevier]
日期:2023-04-29
卷期号:324: 121745-121745
被引量:18
标识
DOI:10.1016/j.lfs.2023.121745
摘要
Circular RNAs (circRNAs) are important regulators in breast cancer progression. However, the underlying mechanism of circRNAs functions in breast cancer remain largely unclear.To investigate the circRNAs expression pattern in breast cancer, high-throughput circRNA microarray assay was used. The top up-regulated circRNA, circZFAND6, was submitted to further experiments, including cell counting kit-8 (CCK-8) assay, colony formation assay, transwell assay and mouse xenograft assay. To investigate the underlying mechanism of circZFAND6 function in breast cancer progression, luciferase reporter assay and RNA immunoprecipitation (RIP) assay were conducted.We found a novel circRNA, circZFAND6, was up-regulated in breast cancer tissues and cell lines. Inhibition of circZFAND6 reduced proliferation and metastasis of breast cancer. Mechanically, circZFAND6 acted as a competing endogenous RNA (ceRNA) to sponge miR-647 and increase fatty acid synthase (FASN) expression. And eukaryotic translation initiation factor 4A3 (EIF4A3) was found to bind to circZFAND6 pre-mRNA transcript upstream region, leading to the high expression of circZFAND6 in breast cancer. Inhibition of EIF4A3 also suppressed proliferation and metastasis of breast cancer.EIF4A3-induced circZFAND6 up-regulation promoted proliferation and metastasis of breast cancer through the miR-647/FASN axis. Our results uncovered a possible mechanism underlying breast cancer progression and might provide a breast cancer treatment target.
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