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. 2022 Aug 16;61(2):506–520. doi: 10.1007/s10528-022-10263-y

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© The Author(s) 2022

Open AccessThis 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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Fig. 5 — miR-29c promoted cell migration and invasion of NSCLC. NSCLC cells were transfected with miR-29c mimics and Anti-miR-29c, and the migration and invasion abilities were analyzed. A and E Wound healing assay of cell migration ability in A549 (A) and H1299 (E) cells. B and F Transwell migration assay of cell migration capability in A549 (B) and H1299 (F) cells. C and G Transwell invasion assay of cell invasion ability in A549 (C) and H1299 (G) cells. D and H Western blot analysis of cancer metastasis-associated proteins (MMP2/9, TIMP1/2) in A549 (D) and H1299 (H) cells. *P < 0.05, **P < 0.01, ***P < 0.001