Li Xuzhao, Wang Nianhua, Leng Haibin, Yuan Huichun, Xu Lixin
Department of Neurosurgery, The First People's Hospital of Changde City, Changde City, 415000, Hunan, China.
Department of Neurosurgery, The First People's Hospital of Changde City, No.818, Renmin Road, Changde, 415000, Hunan, China.
Metab Brain Dis. 2022 Dec;37(8):2979-2993. doi: 10.1007/s11011-022-01069-3. Epub 2022 Oct 27.
Temozolomide (TMZ) resistance limits its use in glioblastoma (GBM). Exosomes can carry circular RNAs (circRNAs) to regulate chemoresistance. To date, the role of exosomal hsa_circ_0043949 (circ_0043949) in GBM resistance to TMZ is unclear. Relative expression of circ_0043949 in clinical samples, GBM cell lines, and exosomes was detected by reverse transcription-quantitative polymerase chain reaction (RT-qPCR). The half-maximal inhibitory concentration (IC) of TMZ, cell proliferation, apoptosis, invasion, and migration were analyzed via MTT, EdU, flow cytometry, transwell, and wound-healing assays. Relative protein levels were evaluated by western blotting. Target relationship was predicted by bioinformatics analysis and validated by dual-luciferase reporter and RNA pull-down assays. Exosomes were isolated by ultracentrifugation and verified by transmission electron microscopy, nanoparticle tracking analysis (NTA), and western blotting. The effect of exosomal circ_0043949 on TMZ resistance was validated by xenograft assay. Higher expression of circ_0043949 was gained in TMZ-resistant GBM samples and cells. Inhibition of circ_0043949 reduced TMZ resistance via decreasing IC of TMZ, repressing proliferation, invasion, migration, and inducing apoptosis in TMZ-resistant GBM cells. Circ_0043949 mediated integrinalpha1 (ITGA1) expression via function as a miR-876-3p sponge. Circ_0043949 was also upregulated in TMZ-resistant GBM cells-derived exosomes, and exosomal circ_0043949 increased the resistance of TMZ-resistant GBM cells to TMZ in xenograft models. TMZ-resistant GBM cells-derived exosomal circ_0043949 promoted TMZ resistance via upregulating ITGA1 expression via sequestering miR-876-3p, offering a potential target for the treatment of TMZ resistance in GBM.
替莫唑胺(TMZ)耐药性限制了其在胶质母细胞瘤(GBM)中的应用。外泌体可携带环状RNA(circRNA)来调节化疗耐药性。迄今为止,外泌体hsa_circ_0043949(circ_0043949)在GBM对TMZ的耐药性中的作用尚不清楚。通过逆转录定量聚合酶链反应(RT-qPCR)检测circ_0043949在临床样本、GBM细胞系和外泌体中的相对表达。通过MTT、EdU、流式细胞术、Transwell和伤口愈合试验分析TMZ的半数最大抑制浓度(IC)、细胞增殖、凋亡、侵袭和迁移。通过蛋白质印迹法评估相关蛋白水平。通过生物信息学分析预测靶标关系,并通过双荧光素酶报告基因和RNA下拉试验进行验证。通过超速离心分离外泌体,并通过透射电子显微镜、纳米颗粒跟踪分析(NTA)和蛋白质印迹法进行验证。通过异种移植试验验证外泌体circ_0043949对TMZ耐药性的影响。在TMZ耐药的GBM样本和细胞中,circ_0043949表达较高。抑制circ_0043949可通过降低TMZ的IC、抑制TMZ耐药GBM细胞的增殖、侵袭、迁移并诱导其凋亡来降低TMZ耐药性。Circ_0043949通过充当miR-876-3p海绵介导整合素α1(ITGA1)的表达。在TMZ耐药GBM细胞来源的外泌体中,circ_0043949也上调,并且在异种移植模型中,外泌体circ_0043949增加了TMZ耐药GBM细胞对TMZ的耐药性。TMZ耐药GBM细胞来源的外泌体circ_0043949通过螯合miR-876-3p上调ITGA1表达来促进TMZ耐药性,为GBM中TMZ耐药性的治疗提供了一个潜在靶点。