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. 2022 May 10;37(4):246–255. doi: 10.1089/cbr.2020.3587

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© Dandan Mao et al. 2022; Published by Mary Ann Liebert, Inc.

This Open Access article is distributed under the terms of the Creative Commons License [CC-BY] (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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FIG. 2. — SNHG6 regulated the viability, migration, invasion, and EMT of HP75 cells. (A) SNHG6 overexpression model and knockdown model were established, respectively, using HP75 cells, and the expression level of SNHG6 was detected by qRT-PCR. (B) CCK-8 assay was conducted to detect the proliferation of HP75 cells. (C, D) Transwell migration assay was used to detect migration and invasion of HP75 cells. (E) Western blot was carried out to detect the expressions of E-cadherin and vimentin after SNHG6 was upregulated or downregulated in HP75 cells. **p < 0.01; ***p < 0.001. CCK-8, cell counting kit-8; EMT, epithelial–mesenchymal transition.