小RNA
细胞因子
癌症研究
同源盒
细胞生物学
生物
骨肉瘤
细胞生长
体内
转移
受体
化学
基因
癌症
转录因子
免疫学
遗传学
作者
Hanji Huang,Dejie Lu,Kanglu Li,Mingjun Zheng,Xiong Qin,Xiaofei Cui,Ying Chen,Chaotao Chen,Nanchang Huang,Li Zheng,Jinmin Zhao,Bo Zhu
标识
DOI:10.1016/j.bcp.2023.115667
摘要
Circular RNAs (circRNAs), a subclass of noncoding RNAs, have been demonstrated to play an essential role in osteosarcoma (OS) development. However, there is still a significant gap in investigating its biological functions and underlying molecular mechanisms, and novel targets of circRNAs have yet to be fully explored. Herein, we found that hsa_circ_0007031 is noticeably raised in OS clinical tissues and cell lines. Hsa_circ_0007031 accelerates OS cell proliferation and migration in vitro and tumor growth and metastasis in vivo and is strongly linked with the stemness of cancer stem cells in OS. Mechanistically, hsa_circ_0007031 shares miRNA response elements with Homeobox B6 (HOXB6), which is identified as a novel pro-tumorigenic gene of OS. Hsa_circ_0007031 competitively binds to miR-196a-5p to prevent miR-196a-5p from lowering the level of HOXB6, which modulates chemokines of cytokine-cytokine receptor interaction signaling pathway and finally promotes OS malignant behavior. In summary, our data unveiled that hsa_circ_0007031/miR-196a-5p/HOXB6 axis-mediated cytokine-cytokine receptor interaction facilitates the progression of OS and maintains the properties of tumor stem cells, which could be a promising therapeutic target for OS.
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