三阴性乳腺癌
下调和上调
癌症研究
转移
脑转移
乳腺癌
小RNA
自噬
免疫印迹
竞争性内源性RNA
生物
生物标志物
癌症
医学
内科学
细胞凋亡
基因
长非编码RNA
生物化学
作者
Song Wu,Jibu Lu,Hongbo Zhu,Feiyue Wu,Yunxian Mo,Liping Xie,Cailu Song,Lingrui Liu,Xiaoming Xie,Yuehua Li,H. Helen Lin,Hailin Tang
出处
期刊:Cancer Letters
[Elsevier]
日期:2024-01-01
卷期号:581: 216508-216508
被引量:26
标识
DOI:10.1016/j.canlet.2023.216508
摘要
Among patients with triple-negative breast cancer (TNBC), distant metastasis is the leading cause of death. Our previous studies have shown that TNBC progression is greatly facilitated by circKIF4A, but uncertainty remains regarding its role in TNBC brain metastasis and the molecular mechanism. In this study, we found notable upregulation of circKIF4A in TNBC cell lines and brain metastases. Inhibition of circKIF4A impaired the ability of TNBC to proliferate, migrate, and cause brain metastasis. Luciferase reporter assays confirmed that circKIF4A competed for binding to miR-637 with STAT3 3' UTR. Western blot analysis revealed that inhibition of circKIF4A decreased STAT3 and p62 expression, while increased the LC3B-II/LC3B-I ratio and the expression of Beclin, indicating that downregulation of circKIF4A induced autophagy by competing with STAT3 for binding to miR-637. By employing a competitive endogenous RNA (ceRNA) mechanism, the circKIF4A-miR-637-STAT3 axis coordinates brain metastasis in TNBC. circKIF4A can therefore be used as a prognostic biomarker for brain metastasis in TNBC and as a therapeutic target.
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