Circular RNA hsa_circ_0001306 Functions as a Competing Endogenous RNA to Regulate FBXW7 Expression by Sponging miR-527 in Hepatocellular Carcinoma.
Circular RNA hsa_circ_0001306 Functions as a Competing Endogenous RNA to Regulate FBXW7 Expression by Sponging miR-527 in Hepatocellular Carcinoma.
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环状 RNA hsa_circ_0001306 作为竞争性内源 RNA 通过海绵 miR-527 在肝细胞癌中调节 FBXW7 表达
DOI:
10.7150/jca.61381
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发表时间:
2021
影响因子:
3.9
通讯作者:
Xue X
中科院分区:
文献类型:
--
作者:
Wu Y;Fan T;Zhao Y;Hu R;Yan D;Sun D;Gao L;Qin L;Xue X
Hepatocellular carcinoma (HCC) is one of the most common types of cancer worldwide. Circular RNAs (circRNAs) have been reported to regulate many types of cancers, including HCC. The purpose of this study was to investigate the potential roles of hsa_circ_0001306 in HCC. Firstly, the downregulation of hsa_circ_0001306 was identified by high‑throughput RNA sequencing and further verified by qRT-PCR. Secondly, we evaluated the effects of hsa_circ_0001306 on HCC cell proliferation, invasion, cell cycle. Finally, we used an animal model to validate the in vitro experimental results. The expression of hsa_circ_0001306 was closely related to tumor size. Knockdown of hsa_circ_0001306 could downregulate F-box and WD repeat domain containing 7(FBXW7), a target of miR-527, thereby promoting HCC cell proliferation and invasion. Furthermore, hsa_circ_0001306 siRNA increased the multiplication rate of HCC tumors. Mechanistic studies indicated that hsa_circ_0001306 acts as a ceRNA for miR-527, which resulted in the reduction of its endogenous target, FBXW7. Hsa_circ_001306 is significantly downregulated in HCC, and the hsa_circ_0001306/miR-527/FBXW7 axis plays an important role in HCC progression.
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影响因子:
7.4
作者:
Xiong DD;Dang YW;Lin P;Wen DY;He RQ;Luo DZ;Feng ZB;Chen G
通讯作者:
Chen G
影响因子:
3.7
作者:
Sticht C;De La Torre C;Parveen A;Gretz N
通讯作者:
Gretz N
影响因子:
5.7
作者:
Mori A;Masuda K;Ohtsuka H;Shijo M;Ariake K;Fukase K;Sakata N;Mizuma M;Morikawa T;Hayashi H;Nakagawa K;Motoi F;Naitoh T;Fujishima F;Unno M
通讯作者:
Unno M
影响因子:
4.1
作者:
Chen, Ling-Ling;Yang, Li
通讯作者:
Yang, Li
DOI:
10.1016/j.ijbiomac.2018.09.076
发表时间:
2019-02-01
影响因子:
8.2
作者:
Jie Si-Tu;Cai, Yi;Li, Zhipeng
通讯作者:
Li, Zhipeng