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. 2023 Oct 16;9:378. doi: 10.1038/s41420-023-01675-9

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© The Author(s) 2023

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. 7 — A GSEA analysis identified a significant enrichment of MEK/ERK signaling in HOXA5 silenced cells. B The expression of phospho-MEK, phospho-ERK, and total MEK and ERK in PCa cells. The transfected PC-3 cells were treated with 10 µM U0126 (a specific MEK/ERK inhibitor). C The viability of PC-3 cells was determined by a CCK-8 assay. D Representative images of migration and invasion and corresponding quantitative results. E Flow cytometry assay with CD133 in PC-3 cells and quantitative results. *P < 0.05, **P < 0.01. Results were presented as mean ± SD of three biological replicates.