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. 2021 Apr 14;30:09636897211007395. doi: 10.1177/09636897211007395

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© The Author(s) 2021

This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).

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Figure 2. — Downregulation of FBXO17 suppresses glioma cell proliferation. We further constructed FBXO17-silencing U251 and SHG44 cells through infection with shRNA1-FBXO17 or shRNA2-FBXO17. U251 and SHG44 cells infected with shRNA-NC served as controls. (A, D) Comparison of mRNA levels of FBXO17 in U251 and SHG44 cells with different infection. (B, E) Comparison of protein levels of FBXO17 in U251 and SHG44 cells with different infections. (C, F) CCK-8 assay was performed to evaluate the proliferation of U251 and SHG44 cells with different infection. *P < 0.05 vs shRNA-NC group.