Department of Hepatobiliary Surgery, 900TH Hospital of Joint Logistics Support Force, Fuzhou, China.
J Biochem Mol Toxicol. 2023 Oct;37(10):e23437. doi: 10.1002/jbt.23437. Epub 2023 Jun 23.
Increasing evidence has displayed the vital influence of lncRNA in tumorigenesis and chemoresistance of cancer treatment. This study investigated the function of lncRNA PTOV1-AS1 in hepatocellular carcinoma (HCC) and its role in sorafenib resistance. The relative expression of lncRNA and miRNA was measured by RT-qPCR. The cellular activities including cell proliferation and invasion were explored by CCK-8 and Transwell assays. Bioinformatics analysis and dual-luciferase reporter assay were used to predict the targeting miRNA of PTOV1-AS1. The expression levels of PTOV1-AS1 were higher in HCC tissues than that in the normal tissues and associated with patients' overall survival. Knockdown of PTOV1-AS1 decreased cell proliferation rate and invasion number. After treatment with different concentrations of sorafenib, the sorafenib-resistant hepatoma cells were conducted. PTOV1-AS1 expression levels were increased in HepG2-SR and Huh7-SR cells. PTOV1-AS1 knockdown repressed the proliferation, invasion, and drug resistance of sorafenib-resistant HCC cells by targeting the expression of miR-505. In conclusion, the expression of PTOV1-AS1 is increased in HCC and sorafenib-resistance HCC cells, as well as is associated with patients' prognosis. Inhibition of PTOV1-AS1 expression can reduce the resistance of sorafenib-resistant HCC cells, which may play a role by targeting the negative regulation of miR-505 expression.
越来越多的证据表明,lncRNA 在肿瘤发生和癌症治疗的化疗耐药中起着至关重要的作用。本研究探讨了长链非编码 RNA PTOV1-AS1 在肝细胞癌(HCC)中的功能及其在索拉非尼耐药中的作用。通过 RT-qPCR 测量 lncRNA 和 miRNA 的相对表达。通过 CCK-8 和 Transwell 测定法研究细胞活性,包括细胞增殖和侵袭。生物信息学分析和双荧光素酶报告基因实验用于预测 PTOV1-AS1 的靶向 miRNA。PTOV1-AS1 的表达水平在 HCC 组织中高于正常组织,与患者的总生存期相关。敲低 PTOV1-AS1 降低了细胞增殖率和侵袭数量。用不同浓度的索拉非尼处理后,进行索拉非尼耐药肝癌细胞。HepG2-SR 和 Huh7-SR 细胞中 PTOV1-AS1 表达水平增加。通过靶向 miR-505 的表达,PTOV1-AS1 敲低抑制了索拉非尼耐药 HCC 细胞的增殖、侵袭和耐药性。总之,PTOV1-AS1 的表达在 HCC 和索拉非尼耐药 HCC 细胞中增加,并与患者的预后相关。抑制 PTOV1-AS1 的表达可以降低索拉非尼耐药 HCC 细胞的耐药性,这可能通过负调控 miR-505 的表达来发挥作用。