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. 2017 Oct 24;15(1):191–197. doi: 10.3892/etm.2017.5370

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Copyright: © Qin 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 2. — MDC1-AS inhibits the proliferation of human gastric cancer cells. (A) The relative expression of MDC1-AS mRNA in MKN28 cells was examined using RT-qPCR analysis after cells were transfected with an MDC1-AS-expressing plasmid. (B) MDC1-AS mRNA expression in MKN45 cells was examined with RT-qPCR analysis after cells were transfected with shRNA directed against MDC1-AS. Cell proliferation was examined in (C) MKN28 cells after treatment with the MDC1-AS expressing plasmid and (D) MKN45 cells after treatment with shRNA directed against MDC1-AS for 5 consecutive days. *P<0.05 vs. the control group. MDC1-AS, mediator of DNA damage checkpoint protein 1-antisense RNA; RT-qPCR, reverse transcription-quantitative polymerase chain reaction; shRNA, small hairpin RNA.