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. 2021 Mar 19;21:178. doi: 10.1186/s12935-021-01872-5

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© The Author(s) 2021

Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 7 — The effect of stable transfection of pre-mir-34a on the cell proliferation. The flow cytometric assessment using CFSE labeling demonstrated that total number of KatoIII-pGFPC1-34a and KatoIII-pGFPC1- empty cells were proliferated at day1, but KatoIII-pGFPC1-34a cells multiplied slowly during the 3 days in culture. Overlay plots were displayed at the bottom