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. 2020 Jun 4;11(6):420. doi: 10.1038/s41419-020-2629-3

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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 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. 2 — The expression of HOXA5 in human cervical cancer cell lines was detected using immunocytochemistry (a) and western blot (b). Stably transfected HOXA5-modified cervical cancer cell lines were identified by western blotting (c, f, i, l). The proliferation was detected using growth curves in HeLa-GFP and HeLa-HOXA5 cells (d), SiHa-GFP and SiHa-HOXA5 cells (g), C-33A-shCtrl and C-33A-shHOXA5 cells (j), and C-33A-criCtrl and C-33A-cri HOXA5 cells (m). The viability was detected by the MTT assay in HeLa-GFP and HeLa-HOXA5 cells (e), SiHa-GFP and SiHa-HOXA5 cells (h), C-33A-shCtrl and C-33A-shHOXA5 cells (k), and C-33A-criCtrl and C-33A-cri HOXA5 cells (n). Data were statistically analyzed with Student’s t-test and values are shown as the mean ± SD. *p < 0.05, **p < 0.01, ***p < 0.001.