Jing FanJing, Shi YunYan, Jiang Dong, Li Xiao, Sun JiaLin, Guo Qie
Department of Clinical Pharmacy, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, 266003, People's Republic of China.
Navy Qingdao Special Service Rehabilitation Center, Qingdao, Shandong, 266003, People's Republic of China.
Immunotargets Ther. 2024 Nov 26;13:643-659. doi: 10.2147/ITT.S463556. eCollection 2024.
Sorafenib, an orally active potent tyrosine kinase inhibitor (TKI), represented a primary treatment in patients with advanced hepatocellular carcinoma (HCC). Unfortunately, sorafenib resistance was regarded as a huge obstacle for HCC treatment.
RNA-sequencing including circRNA Sequencing (circRNA-Seq) for circular RNAs (circRNAs), miRNA Sequencing (miRNA-Seq) for microRNAs (miRNAs), as well as mRNA Sequencing (mRNA-Seq) for mRNAs in , were performed. Then, interaction correlation analysis between differentially expressed circRNAs and miRNAs and their target genes in Huh7/SOR and SMMC7721/SOR cells was exhibited. The "circRNA-miRNA-mRNA" network was constructed through and . Furthermore, for the downstream genes involved in the "circRNA-miRNA-mRNA" network was implemented. and in vivo were used to determine the mechanisms promoting sorafenib resistance in HCC, where the "circRNA-miRNA-mRNA" network is clearly involved in.
circ_0001944 and circ_0078607 with upregulation and 2 downregulated expressed circRNAs (circ_0002874 and circ_0069981), as well as 11 upregulated miRNAs including miR-193a-5p, miR-197-3p, miR-27a-5p, miR-551b-5p, miR-335-3p, miR-767-3p, miR-767-5p, miR-92a-1-5p, miR-92a-3p, miR-3940-3p, and miR-664b-3p and 3 downregulated expressed miRNAs (miR-1292-5p, let-7c-5p, and miR-99a-5p) in sorafenib-resistant HCC cells were determined. Among these non-coding RNAs (ncRNAs), circ_0001944 and miR-1292-5p should not be drop out of sight; circ_0001944 has been proved to target miR-1292-5p to inhibit its expression in HCC. Subsequent findings also raise that miR-1292-5p directly targeted the 3'-noncoding region (3'-UTR) of mRNA. Furthermore, circ_0001944 targets the miR-1292-5p/FBLN2 axis to inhibit cell ferroptosis in which the indicated regulators associated with iron overload and lipid peroxidation were "rearranged". Most importantly, circ_0001944 advanced sorafenib resistance in HCC through mitigating ferroptosis, where the miR-1292-5p/FBLN2 axis cannot be left unrecognized.
Circ_0001944 is a putative target for reversing sorafenib resistance in HCC. Our findings are expected to provide new targets and new directions for sorafenib sensitization in the treatment of HCC.
索拉非尼是一种口服有效的强效酪氨酸激酶抑制剂(TKI),是晚期肝细胞癌(HCC)患者的主要治疗药物。不幸的是,索拉非尼耐药被认为是肝癌治疗的巨大障碍。
进行了RNA测序,包括用于环状RNA(circRNA)的环状RNA测序(circRNA-Seq)、用于微小RNA(miRNA)的微小RNA测序(miRNA-Seq)以及用于mRNA的mRNA测序(mRNA-Seq)。然后,展示了Huh7/SOR和SMMC7721/SOR细胞中差异表达的circRNA与miRNA及其靶基因之间的相互作用相关性分析。通过……构建了“circRNA-miRNA-mRNA”网络。此外,对“circRNA-miRNA-mRNA”网络中涉及的下游基因进行了……。体内……用于确定促进肝癌中索拉非尼耐药的机制,其中“circRNA-miRNA-mRNA”网络明显参与其中。
确定了索拉非尼耐药肝癌细胞中上调的circ_0001944和circ_0078607以及2个下调表达的circRNA(circ_0002874和circ_0069981),以及11个上调的miRNA,包括miR-193a-5p、miR-197-3p、miR-27a-5p、miR-551b-5p, miR-335-3p、miR-767-3p、miR-767-5p、miR-92a-1-5p、miR-92a-3p、miR-3940-3p和miR-664b-3p,以及3个下调表达的miRNA(miR-1292-5p、let-7c-5p和miR-99a-5p)。在这些非编码RNA(ncRNA)中,circ_0001944和miR-1292-5p不容忽视;已证明circ_0001944靶向miR-1292-5p以抑制其在肝癌中的表达。随后的研究还发现,miR-1292-5p直接靶向……mRNA的3'非编码区(3'-UTR)。此外,circ_0001944靶向miR-1292-5p/FBLN2轴以抑制细胞铁死亡,其中与铁过载和脂质过氧化相关的所示调节因子被“重新排列”。最重要的是,circ_0001944通过减轻铁死亡促进肝癌中的索拉非尼耐药,其中miR-1292-5p/FBLN2轴不容忽视。
Circ_0001944是逆转肝癌中索拉非尼耐药的一个假定靶点。我们的数据有望为肝癌治疗中索拉非尼增敏提供新的靶点和新的方向。