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. 2019 Apr 23;11:3493–3509. doi: 10.2147/CMAR.S195137

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© 2019 Liu et al.

This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).

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SMARCE1 promotes GC cell proliferation in vitro.

Notes: (A) GC cell viability was assessed using the CCK-8 assay after transfection with SMARCE1, shSMARCE1, or control lentiviruses. (B) The proliferative capacity was evaluated through a colony formation assay and quantitative data of the colony number are shown. (C) Representative images of SMARCE1 and ki-67 IHC staining in 80 human GC tissues. Magnification ×400; (D) Correlation analysis revealed a strong correlation between SMARCE1 and ki-67 in GC tissues. The data are shown as the mean ± SD of three independent experiments. **P<0.01; ***P<0.001.

Abbreviations: OD, optical density; GC, gastric cancer; CCK-8, Cell Counting Kit-8 .