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. 2018 Feb 7;9(2):167. doi: 10.1038/s41419-017-0241-y

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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. 8 — Identification of predicted miRNA response element (MRE) using in silico screening methods (a); Levels of EGFR/Akt1/mTOR signaling axis proteins’ in LNCaP mock and 5-Aza-CdR-treated cell lines (b) and in PC3 Sh-scramble and Sh-MYC (c) by western blot analysis: mTOR 289 KDa, EGFR 134 KDa, Akt1 62 KDa, and β-Actin 42 KDa (numbers represent the average fold-change compared with LNCaP mock for three independent experiments)