Abstract | OBJECTIVE: METHODS: KCNQ1OT1 expression was detected in ESCC tissues using quantitative real-time polymerase chain reaction (qRT-PCR). Cell proliferation, apoptosis, migration, and invasion were detected by the CCK-8 assay, EdU assay, flow cytometry analysis, and Transwell experiments, respectively. Bioinformatics analysis, luciferase reporter experiments, and RNA immunoprecipitation assays were used to predict and validate the regulatory relationships between KCNQ1OT1, microRNA-133b (miR-133b) and epidermal growth factor receptor (EGFR). RESULTS: KCNQ1OT1 expression was remarkably upregulated in ESCC tissues and cell lines. Overexpression of KCNQ1OT1 markedly promoted ESCC cell proliferation, migration, and invasion and enhanced the expression of N-cadherin, MMP-2, and MMP-9, but inhibited apoptosis and E-cadherin expression in ESCC cell lines; KCNQ1OT1 knockdown exerted the opposite effects. KCNQ1OT1 could directly bind to miR-133b and suppress its expression, and miR-133b reversed the effects of KCNQ1OT1 overexpression in ESCC cells. MiR-133b reduced the expression of epidermal growth factor receptor (EGFR); further, KCNQ1OT1 activated the phosphatidylinositol 3-kinase/AKT serine/threonine kinase 1 (PI3K/AKT) signaling pathway by repressing miR-133b repression and indirectly upregulating EGFR. KCNQ1OT1 expression was positively correlated with EGFR mRNA expression and negatively correlated with miR-133b expression. CONCLUSION: KCNQ1OT1 facilitates ESCC progression by sponging miR-133b and activating the EGFR/PI3K/AKT pathway.
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Authors | Haitao Xu, Jing Miao, Shuai Liu, Hongjian Liu, Lianguo Zhang, Qingguang Zhang |
Journal | Clinics (Sao Paulo, Brazil)
(Clinics (Sao Paulo))
Vol. 76
Pg. e2175
( 2021)
ISSN: 1980-5322 [Electronic] United States |
PMID | 33909822
(Publication Type: Journal Article)
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Chemical References |
- KCNQ1 Potassium Channel
- KCNQ1 protein, human
- MicroRNAs
- RNA, Long Noncoding
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Topics |
- Cell Proliferation
(genetics)
- Esophageal Neoplasms
(genetics)
- Esophageal Squamous Cell Carcinoma
(genetics)
- Humans
- KCNQ1 Potassium Channel
(genetics)
- MicroRNAs
(genetics)
- Phosphatidylinositol 3-Kinases
- RNA, Long Noncoding
(genetics)
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