Zhang Dan, Huang Haiping, Sun Yangguang, Cheng Fuwei, Zhao Shuangping, Liu Jisheng, Sun Peng
Department of ENT, the First Affiliated Hospital of Soochow University, Suzhou, China.
Transl Cancer Res. 2022 Jul;11(7):2348-2358. doi: 10.21037/tcr-22-1645.
Circular RNAs (circRNAs) are a new family of endogenous non-coding RNAs generated by a covalently closed loop, and a mounting body of data suggests they control gene expression. While the homeodomain-interacting protein kinase-2 () is generated from the homeodomain-interacting protein kinase 2 () gene, the function of in nasopharyngeal cancer (NPC) along with the responsible mechanisms are still unclear.
RNA-sequencing data was utilized to determine the differentially expressed circRNAs, and was established as a novel prospective circRNA. The expressions of circRNAs along with messenger RNAs (mRNAs) in NPC tissues and cells was assessed via quantitative real-time polymerase chain reaction (qRT-PCR), and the transfection of NPC cells with plasmids and was adopted to explore the effects of in NPC. Western blotting was adopted to assess the expressions of and , while Cell Counting Kit (CCK)-8 assay coupled with colony-forming assay were utilized to assess the biological functions. The expression of nuclear and cytoplasmic was detected via nucleocytoplasmic separation assay.
Herein, we established that was upregulated in NPC tissues. Over-expression of promoted cell proliferation and , and further studies revealed it inhibited the protein level of in a post-transcriptional pattern, decreasing expression and suppressing the proliferation of NPC.
Our findings demonstrated elevated facilitated the cell proliferation of NPC cells via the axis, suggesting might be an oncogene to promote the process of NPC and could be a novel treatment target for its management.
环状RNA(circRNAs)是一类新的内源性非编码RNA,由共价闭环产生,越来越多的数据表明它们可调控基因表达。虽然同源结构域相互作用蛋白激酶2()由同源结构域相互作用蛋白激酶2()基因产生,但在鼻咽癌(NPC)中的功能及其相关机制仍不清楚。
利用RNA测序数据确定差异表达的circRNAs,并将确立为一种新的有前景的circRNA。通过定量实时聚合酶链反应(qRT-PCR)评估NPC组织和细胞中circRNAs以及信使RNA(mRNAs)的表达,并采用质粒和转染NPC细胞来探究在NPC中的作用。采用蛋白质免疫印迹法评估和的表达,同时利用细胞计数试剂盒(CCK)-8法和集落形成试验评估生物学功能。通过核质分离试验检测核质的表达。
在此,我们证实了在NPC组织中上调。的过表达促进细胞增殖和,进一步研究表明它以转录后模式抑制的蛋白水平,降低表达并抑制NPC的增殖。
我们的研究结果表明,升高通过轴促进NPC细胞的增殖,提示可能是促进NPC进程的癌基因,并且可能是其治疗的新靶点。