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Additional file 13: of A positive feed-forward loop between LncRNA-URRCC and EGFL7/P-AKT/FOXO3 signaling promotes proliferation and metastasis of clear cell renal cell carcinoma

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https://springernature.figshare.com/articles/dataset/Additional_file_13_of_A_positive_feed-forward_loop_between_LncRNA-URRCC_and_EGFL7_P-AKT_FOXO3_signaling_promotes_proliferation_and_metastasis_of_clear_cell_renal_cell_carcinoma/7961360/1
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Figure S4. A: Bioinformatics analysis of potential FOXO3 binding site on URRCC promoter by online software RegRNA 2.0. B: Correlation between URRCC and FOXO3 in mRNA level in cell lines. C and D: The mRNA level of URRCC and EGFL7 were detected by qRT-PCR in A498 and OSRC-2 cells after transfection with si-NC or si-FOXO3. E and F: The mRNA level of URRCC and EGFL7 were detected by qRT-PCR in A498 and OSRC-2 cells after transfection with NC or oe-FOXO3. G and H: Cell apoptosis assays by flow cytometry in A498 cell lines. (ZIP 209 kb)

补充图S4。A:通过在线软件RegRNA 2.0对URRCC启动子上的潜在FOXO3结合位点开展生物信息学分析。B:细胞系中URRCC与FOXO3的mRNA水平相关性分析。C、D:在转染阴性对照小干扰RNA(si-NC)或FOXO3靶向小干扰RNA(si-FOXO3)的A498及OSRC-2细胞中,采用实时荧光定量逆转录聚合酶链反应(qRT-PCR)检测URRCC与EGFL7的mRNA表达水平。E、F:在转染阴性对照(NC)或FOXO3过表达载体(oe-FOXO3)的A498及OSRC-2细胞中,采用qRT-PCR检测URRCC与EGFL7的mRNA表达水平。G、H:采用流式细胞术对A498细胞系进行细胞凋亡检测实验。(ZIP 209 KB)
提供机构:
Zhang, Jin; Zhu, Rujian; Xue, Wei; Zhang, Haimin; Chen, Yonghui; Zhai, Wei; Zheng, Junhua; Huang, Yiran; Gong, Dongkui; Ma, Junjie
创建时间:
2019-04-06
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