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. 2021 Jan 12;11:685. doi: 10.1038/s41598-020-80097-4

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© The Author(s) 2021

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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miR-197-3p suppresses the expression of inflammatory cytokines and genes. (a) qPCR measurement of IL-1β, IL-18, MEFV, TNF-α, and TGF-β gene expression levels in miR-197-3p or control sequence-transfected (scramble/mimic control) SW982 cell line. Data represent the mean ± standard deviation from three independent experiments. * P < 0.05; ** P < 0.01, Student’s t-test (two-tailed). (b) qPCR measurement of IL-1β, IL-18, MEFV, TNF-α, and TGF-β gene expression levels in miR-197-3p or control sequence-transfected (scramble/mimic control) THP-1 cell line. Data represent the mean ± standard deviation from three independent experiments. *P < 0.05; ** P < 0.01, Student’s t-test (two-tailed). (c) miR-197-3p expression level in SW982 cell line after TNF-α and TGF-β applications. Data represent the mean ± standard deviation from three independent experiments. * P < 0.05, Student’s t-test (two-tailed).