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. 2019 Jul 17;23(9):6411–6428. doi: 10.1111/jcmm.14533

Figure 6.

Figure 6

RNA‐FISH and CHIP reveal that silencing of lncRNA H19 inhibits methylation of CDH1. A, expression of H19 in lung adenocarcinoma tissues and normal tissues retrieved from the TCGA database; B, subcellular localization of lncRNA H19 detected by RNA‐FISH. C, CpG island in the CDH1 promoter region based on the Meth Primer software; D, the binding site between lncRNA H19 and CDH1 promoter predicted by biological website; E, the luciferase intensity of the CDH1 wild‐type promoter region detected by luciferase reporter gene; F, the luciferase intensity of the M‐CDH1 determined by luciferase reporter gene; G, statistical chart of CHIP. lncRNA H19, long non‐coding RNA H19; CDH1, E‐cadherin; NC, negative control; DMSO, dimethylsulfoxide; RNA‐FISH, RNA fluorescence in situ hybridization; ChIP, chromatin immunoprecipitation; M‐CDH1, methylated CDH1; DNMT1, DNA methyltransferase 1; DNMT3A, DNA methyltransferase 3A; GAPDH, glyceraldehyde‐3‐phosphate dehydrogenase. *P < .05 vs the NC group; # P < .05 vs the IgG group. The measurement data are presented as mean ± standard deviation, analysed by Student's t test. n = 3. The experiment was independently repeated three times