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. 2022 Jun 17;12:881022. doi: 10.3389/fonc.2022.881022

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Copyright © 2022 Wang, Wang, Li, Niu, Liang, Liu, Liu and Ge

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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ELFN1-AS1 promoted the proliferation, migration and invasion of OS cells. (A) RT-qPCR analysis of ELFN1-AS1 level in 143B and MG63 cells transfected with ELFN1-AS1 siRNA1 or ELFN1-AS1 siRNA2 (n = 3). (B) RT-qPCR analysis of ELFN1-AS1 level in 143B and MG63 cells transfected with pcDNA3.1 ELFN1-AS1 (n = 3). (C, D) 143B and MG63 cells were transfected with pcDNA3.1 ELFN1-AS1 or ELFN1-AS1 siRNA1. CCK-8 assay was applied to measure cell viability (n = 3). (E) EdU staining assay was applied to detect cell proliferation (n = 3). (F) Flow cytometry assay was applied to determine cell apoptosis. (G) Transwell migration and (H) invasion assays were applied to determine cell migration and invasion (n = 3). The significance between groups was analyzed by one-way ANOVA. **P < 0.01.