Department of General Surgery, Xiangya Hospital, Central South University , Changsha , P.R.China.
Department of General Surgery, The Second Xiangya Hospital, Central South University , Changsha , P.R.China.
Cell Cycle. 2019 Nov;18(21):2939-2953. doi: 10.1080/15384101.2019.1664223. Epub 2019 Sep 16.
: Hepatocellular carcinoma (HCC) afflicts more than half a million people each year worldwide. It was reported that circ_0015756 was up-regulated in HCC, but the mechanism did not extensively studied. : we collected 24 paired cancerous and noncancerous liver tissues surgically resected from HCC patients. HCC cell proliferation, invasion, migration and apoptosis were evaluated using MTT assay, Transwell assay, scratch test and Annexin-V/PI staining respectively. Interactions between circ_0015756 and miR-7, miR-7 and FAK were further validated by the luciferase reporter assay. Tumor xenografts of HCC cells with circ_0015756 knockdown were established in nude mice. : The expression level of circ_0015756 was increased and the expression level of miR-7 was diminished in cancerous liver tissues relative to noncancerous liver tissues. Circ_0015756 knockdown was shown to increase the expression of miR-7, reduce the proliferation, invasion, migration and resistance to apoptosis, and down-regulate the expression of FAK in HCC. We found miR-7 impaired expression of FAK to inhibit HCC cells, suggesting that miR-7 is responsible for the dysfunction of FAK. Importantly, we showed circ_0015756 could up-regulate FAK via targeting miR-7. These findings were reproduced that circ_0015756 knockdown decreased HCC xenograft growth. : Our present study reveals a model of HCC development that is composed of circ_0015756, miR-7 and FAK. Modulation of their levels exhibits a promise in the treatment of HCC. HCC: hepatocellular carcinoma; circRNAs: circular RNAs; miRNA/miR: microRNA; miR-7: microRNA-7; FAK: focal adhesion kinase; KLF-4: kruppel like factor 4; DKK1: dickkopf WNT signaling pathway inhibitor 1; ccRCC: clear cell renal cell carcinoma; PI3K: phosphoinositide 3-kinase; Ct: comparative threshold cycle; RPMI: Roswell Park Memorial Institute; FBS: fetal bovine serum; RT: reverse transcription; qPCR: quantitative polymerase chain reaction; RIPA: radioimmunoprecipitation assay; SDS-PAGE: sodium dodecyl sulfate-polyacrylamide gel electrophoresis; PVDF: polyvinylidene difluoride; GAPDH: glyceraldehyde-3-phosphate dehydrogenase; MTT: 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide; DMSO: dimethyl sulfoxide; DMEM: Dulbecco's modified Eagle's medium; PI: propidium iodide; SPF: specific pathogen-free; SD: standard deviation; p-Akt: phosphorylated-Akt; shRNAs: small hairpin RNAs; 3'UTR: 3'-untranslated regions.
肝细胞癌 (HCC) 每年在全球范围内影响超过 50 万人。据报道,circ_0015756 在 HCC 中上调,但该机制尚未广泛研究。
我们收集了 24 对肝癌患者手术切除的癌组织和非癌组织。通过 MTT 检测、Transwell 检测、划痕试验和 Annexin-V/PI 染色分别评估 HCC 细胞的增殖、侵袭、迁移和凋亡。通过荧光素酶报告基因检测进一步验证 circ_0015756 与 miR-7、miR-7 与 FAK 之间的相互作用。用带有 circ_0015756 敲低的 HCC 细胞建立裸鼠肿瘤异种移植模型。
circ_0015756 的表达水平在癌组织中升高,而 miR-7 的表达水平在癌组织中降低相对非癌组织。circ_0015756 敲低显示 miR-7 的表达增加,增殖、侵袭、迁移和抗凋亡能力降低,FAK 的表达下调。我们发现 miR-7 通过靶向 FAK 抑制 HCC 细胞,表明 miR-7 是 FAK 功能障碍的原因。重要的是,我们表明 circ_0015756 通过靶向 miR-7 上调 FAK。这些发现重现了 circ_0015756 敲低降低 HCC 异种移植瘤生长的现象。
我们目前的研究揭示了一个由 circ_0015756、miR-7 和 FAK 组成的 HCC 发展模型。调节它们的水平在 HCC 治疗中有很好的应用前景。
肝细胞癌;circRNAs:环状 RNA;miRNA/miR:微 RNA;miR-7:微 RNA-7;FAK:粘着斑激酶;KLF-4:Krüppel 样因子 4;DKK1:Dickkopf WNT 信号通路抑制剂 1;ccRCC:透明细胞肾细胞癌;PI3K:磷酸肌醇 3-激酶;Ct:比较阈值循环;RPMI:罗塞勒帕克纪念研究所;FBS:胎牛血清;RT:逆转录;qPCR:定量聚合酶链反应;RIPA:放射性免疫沉淀测定;SDS-PAGE:十二烷基硫酸钠-聚丙烯酰胺凝胶电泳;PVDF:聚偏二氟乙烯;GAPDH:甘油醛-3-磷酸脱氢酶;MTT:3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐;DMSO:二甲基亚砜;DMEM:杜尔贝科改良 Eagle 培养基;PI:碘化丙啶;SPF:特定病原体免费;SD:标准差;p-Akt:磷酸化-Akt;shRNAs:短发夹 RNA;3'UTR:3'-非翻译区。