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. 2017 May 18;14(1):173–180. doi: 10.3892/etm.2017.4477

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Copyright: © Liu 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 miR-30a-5p in gastric cancer tissues and cell lines. (A) RT-qPCR was performed to measured the expression of miR-30a-5p in gastric cancer tissues (n=43) and normal gastric tissues (n=10). **P<0.01 vs. normal. (B) RT-qPCR was performed to measure the expression of miR-30a-5p in T1 stage (n=11) and T2-T4 stage (n=32) gastric cancer. ^##P<0.01 vs. T1. (C) RT-qPCR was performed to measure the relative expression of miR-30a-5p in the human gastric cancer cell lines AGS, HGC27, BGC823 and SGC7901, and the normal gastric mucosa epithelial cell line GES-1, as a control. Data are presented as mean ± standard deviation of at least three independent experiments **P<0.01 vs. normal, ^##P<0.01 vs. T1 and ^&&P<0.01 vs. GES-1. miR, microRNA; RT-qPCR, reverse transcription-quantitative polymerase chain reaction.