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. 2020 Nov 4;10:19020. doi: 10.1038/s41598-020-75817-9

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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 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/.

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Detection of MET mRNA by RT-qPCR. (a) RNA concentration (ng/μL) in RNase-free water; (b) RT-qPCR measurement of MET mRNA in EBC1, H596 and Hs746T cells and their EV isolates. Graphs represent mean ± S.E.M. repeat analysis on samples from n = 3 biological repeats for MET gene transcripts. Statistical analysis was by ANOVA, where p < 0.05(*), p < 0.01(**), p < 0.001(***), p < 0.0001(****).