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. 2020 Jan 23;11(1):61. doi: 10.1038/s41419-020-2247-0

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© The Author(s) 2020

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. 3 — mRNA levels of HOTAIR and SCEL in clinical samples (a) and HUVECs (b) were determined by qRT-PCR. GAPDH served as an internal control. Each bar is a mean ± SD of n = 3 experiments. *P < 0.05. c Protein levels of SCEL, Col1a2, MMP9, and VEGFA in five pairs of samples with mostly increased miR-126 levels were determined by western blotting. GAPDH served as loading control. Data were representative images of n = 3 experiments.