Abstract:Objective To investigate the clinical significanceof expression of long non-coding RNA H19 (LncRNA H19) in esophageal carcinoma and its effect on the metastasis ability of human esophageal cancer cell line TE1 in vitro. Methods Totally 72 cases of esophageal carcinoma and the corresponding adjacent tissues were collected from department of cardio-thoracic surgery in our hospital from June 2015 to March 2017. Real-time fluorescence quantitative PCR (qRT-PCR) was used to detect the expression of LncRNA H19 in tissues, and analyze the relationship between the expression and gender, age, tumor differentiation, TNM stages. Lentivirus transfected the vector expressing LncRNA H19 and empty vector into human esophageal cancer cell line TE1, as the test group and control group. Transwell invasion and migration assay were used to detect the invasion and migration ability of both group cells. Western Bolt assay was used to detect the expression of matrix metalloproteinases-2 (MMP-2) and matrix metalloproteinase -9 (MMP-9). Results The expression of LncRNA H19 in esophageal carcinoma was significantly higher than that in adjacent tissue, and the difference was statistically significant (P < 0.05). Patients with high expression of LncRNA H19 in esophageal cancer tissue compared to those with low expression had lower degree of tissue differentiation and higher lymph node metastasis rate, and the difference was statistically significant (P < 0.05). The expression of LncRNA H19 in test group was significantly higher than that in control group cells, and the difference was statistically significant (P < 0.05). The numbers of invasive and migrating cells in test group were significantly higher than those in the control group, and the differences were statistically significant (P < 0.05). The expressions of MMP-2 and MMP-9 protein in test group were significantly higher than those in the control group, and the differences were statistically significant (P < 0.05). Conclusions LncRNA H19 is highly expressed in esophageal cancer tissues, and can promote the metastasis of esophageal cancer cells by up-regulating the expression of MMP.