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Generation and identification of a thyroid cancer cell line with stable expression of CCDC67 and luciferase reporter genes

机译:CCDC67和荧光素酶报告基因稳定表达的甲状腺癌细胞系的产生和鉴定

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摘要

Coiled-coil domain containing 67 (CCDC67) gene is a tumor suppressor gene that exhibits a significant inhibitory effect on a variety of tumors. Our previous study demonstrated that the upregulation of CCDC67 gene in TPC-1 cells inhibited cell proliferation, migration and invasion, and promoted apoptosis in vitro. However, due to the lack of a suitable cell tool, these results were not validated in vivo. In the present study, a thyroid cancer cell line with stable expression of CCDC67 and luciferase reporter genes was generated and identified. Firstly, cDNA clones of the CCDC67 gene were obtained by reverse transcription using a custom-designed primer. The results of subsequent electrophoresis analysis and sequencing revealed that the cDNA clones of CCDC67 gene were obtained successfully, with a length of 1,862 bp. The lentiviral vectors, containing the CCDC67, luciferase reporter and puromycin acetyltransferase genes, were co-transfected with two plasmids that encode lentiviral structural proteins and envelope proteins into 293T cells. Following ultracentrifugation, the titer of lentivirus was determined by ELISA to be 5.0×108 TU/ml. The constructed lentiviral vector was used to transfect TPC-1 thyroid cancer cells, and stabilization was achieved by puromycin screening. The expression of CCDC67 gene, luciferase activity and tumorigenic ability of the generated cell line were detected. Reverse transcription-qPCR results demonstrated that the expression levels of CCDC67 gene in TPC-1 cells following transfection were increased 194,46.782-fold compared with those in the negative control group (P<0.01). A higher fluorescence intensity was detected in the generated cell line, while no detectable fluorescence was observed in untransfected TPC-1 cells. The tumorigenic ability of TPC-1-Luc-Puromycin-CCDC67 cells was verified by bioluminescence imaging and histopathological analysis using a pulmonary metastasis model. These results demonstrated that a thyroid cancer cell line with stable expression of CCDC67 and luciferase reporter genes was generated successfully. The TPC-1-Luc-Puromycin-CCDC67 cell line may be a helpful tool for further research on CCDC67 in vivo.
机译:包含67(CCDC67)基因的螺旋线圈结构域是一种抑癌基因,对多种肿瘤均表现出明显的抑制作用。我们以前的研究表明,TPC-1细胞中CCDC67基因的上调抑制了细胞的增殖,迁移和侵袭,并促进了细胞凋亡。但是,由于缺少合适的细胞工具,这些结果在体内尚未得到验证。在本研究中,产生并鉴定了具有CCDC67和荧光素酶报道基因稳定表达的甲状腺癌细胞系。首先,使用定制引物通过逆转录获得CCDC67基因的cDNA克隆。随后的电泳分析和测序结果表明,成功获得了CCDC67基因的cDNA克隆,全长1862 bp。将包含CCDC67,荧光素酶报道基因和嘌呤霉素乙酰转移酶基因的慢病毒载体与两个编码慢病毒结构蛋白和包膜蛋白的质粒共转染到293T细胞中。超速离心后,通过ELISA测定慢病毒的滴度为5.0×10 8 TU / ml。构建的慢病毒载体用于转染TPC-1甲状腺癌细胞,并通过嘌呤霉素筛选实现了稳定。检测CCDC67基因的表达,荧光素酶活性和所产生细胞系的致瘤能力。逆转录qPCR结果表明,转染后TPC-1细胞中CCDC67基因的表达水平较阴性对照组高194,46.782倍(P <0.01)。在产生的细胞系中检测到较高的荧光强度,而在未转染的TPC-1细胞中未观察到可检测到的荧光。通过生物发光成像和使用肺转移模型的组织病理学分析证实了TPC-1-Luc-Puromycin-CCDC67细胞的致瘤能力。这些结果证明成功产生了具有CCDC67和荧光素酶报告基因的稳定表达的甲状腺癌细胞系。 TPC-1-Luc-Puromycin-CCDC67细胞系可能是在体内进一步研究CCDC67的有用工具。

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