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. 2019 Sep 13;12:7501–7512. doi: 10.2147/OTT.S209138

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© 2019 Tong 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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ZFAS1 promotes PTC cell proliferation in vivo.

Notes: (A) The stable ZFAS1 knockdown K-1 cells were used for in vivo experiments. The nude mice carrying tumors from control and sh-ZFAS1 group were shown. (B) Tumor volume curves were measured every 1 weeks after the injection of K-1 cells. (C) The stable ZFAS1 overexpression TPC-1 cells were used for in vivo experiments. The nude mice carrying tumors from empty vetor and pcDNA-ZFAS1 group were shown. (D) Tumor volume curves were measured every 1 weeks after the injection of TPC-1 cells. **P<0.01.

Abbreviations: sh, short hairpin RNA.