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. 2020 Jun 19;20:258. doi: 10.1186/s12935-020-01284-x

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© The Author(s) 2020

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 — MiR-223 inhibition enhances the efficacy of cisplatin for NSCLC in vivo. a Representative tumour images (n = 3 per group) were shown. The tumors were treated with control, cisplatin, miR-223 Antagomir, or cisplatin plus miR-223 Antagomir. b Growth curves of xenograft tumors treated with control, cisplatin, miR-223 Antagomir, or cisplatin plus miR-223 Antagomir. *P < 0.05 vs cisplatin. c, d Representative Ki-67 staining and TUNEL of apoptosis images in the treatment groups. **P < 0.01 vs. cisplatin