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. 2018 Jul 11;16(3):3635–3641. doi: 10.3892/ol.2018.9138

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Copyright: © Xu et al.

This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.

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Figure 1. — Expression of DNM1L and its effects on gastric carcinoma cell proliferation. (A) Expression of DNM1L mRNA in AGS, SGC-1901, and MKN-45 cells was determined with RT-qPCR. (B) Stable knockdown of DNM1L mRNA with shRNA in MKN-45 cells. (C) MKN-45 cells transfected with sh-DNM1L and sh-Ctrl were incubated for the indicated times. Proliferation was determined with an MTT assay. (D) Results of the MTT assay (optical density) of cells on day 5. Data are from three separate experiments and are presented as means ± standard error of the mean. DNM1L, dynamin-1-like protein; shRNA, short hairpin RNA; Ctrl, control.