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. 2021 May 27;19:62. doi: 10.1186/s12964-021-00707-0

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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. 4 — Effect of miR-1250-5p overexpression in NHL cells. a and b In SU-DHL-6 (a) and SU-DHL-1 (b) cells, miR-1250-5p mimics were transfected using Lipofectamine 2000, followed by qRT-PCR analysis of miR-1250-5p expression at 48 h after transfection as compared with scramble negative control. c and d Cellular proliferation upon overexpression of miR-1250-5p was analyzed by MTS assay in SU-DHL-6 (c) and SU-DHL-1 (d) cells. e and f Number of dead cells upon overexpression of miR-1250-5p was calculated by trypan blue exclusion assay in SU-DHL-6 (e) and SU-DHL-1 (f) cells. g and h Apoptosis upon overexpression of miR-1250-5p was analyzed by FITC Annexin-V-PI assay in SU-DHL-6 (g) and SU-DHL-1 (h) cells. Columns represented mean ± 1SD from three independent experiments