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. 2018 Jun 7;9(6):688. doi: 10.1038/s41419-018-0706-7

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© The Author(s) 2018

Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 6 — a ALG3 expression was detected by qRT-PCR with co-transfection siFTX and anti-miR-342 in AML cell lines. b Western blot was used to detect ALG3 level in AML cell lines. c FCM showed altered mannose level of different treated AML cell lines through FITC-MAN-M and FITC-ConA. d The viability of AML cells was detected by CCK8 with ADR treatment. e The altered IC₅₀ values were calculated. f With ADR treatment, the colony formation ability was determined. g FCM showed the apoptosis rate of transfected AML cells in response to ADR. Data were the means±SD of triplicate determinants (*p < 0.05)