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. 2020 Oct 1;20:475. doi: 10.1186/s12935-020-01573-5

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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. 3 — miR-138-5p could inhibit chemotherapy resistance of colorectal cancer cells. a In Fluorouracial treated HCT116 cell lines, the relative cell viability of LV-mimics group was lower than LV-mNC group (p < 0.001). b In Fluorouracial treated DLD1 cell lines, LV-inhibitor group was higher than LV-INC group in cell viability (p < 0.001). c In Doxorubicin treated HCT116 cell lines, LV-mimics group was lower than LV-mNC group (p < 0.001). d In Doxorubicin treated DLD1 cell lines, LV-inhibitor group was higher than LV-INC group (p < 0.001). e In Cisplatin treated HCT116 cell lines, LV-mimics group was lower than LV-mNC group (p < 0.001). f In Cisplatin treated DLD1 cell lines, LV-inhibitor group was higher than LV-INC group (p < 0.001)