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Fig. 6 | Journal of Experimental & Clinical Cancer Research

Fig. 6

From: RSK3 switches cell fate: from stress-induced senescence to malignant progression

Fig. 6

Higher RSK3 expression correlates with invasiveness in human Claudin-low breast cancers and increases invasion in an experimental mouse breast cancer model. A Analysis of the METABRIC breast cancer gene expression database. Claudin-low breast tumors were divided into 2 groups by the median of RSK3 expression, the fold change between RSK3 high vs low was calculated for all the genes and GSEA was performed. GSEA enrichment plot related to multicancer invasiveness. B-G Mammary glands were analyzed 4–5 weeks after injection of the indicated MCF10DCIS.com cell populations (Ctrl or constitutively expressing RSK3). B Whole-mount carmine-stained glands analyzed 4–5 weeks after injection of the indicated MCF10DCIS.com cell populations (Ctrl or constitutively expressing RSK3). IS, in situ; INV, invasive; LN, lymph node. Scale bar, 1.5 mm. C H&E staining of nipple-injected glands 4–5 weeks after injection of the indicated MCF10DCIS.com cell populations. Scale bar, 200 µm. D Phenotypic analysis of intraductal xenograft tumors of MCF10DCIS.com cells control or overexpressing RSK3. Analysis was based on whole-mount and H&E staining at 4–5 weeks after intraductal injection (Chi-square test). EG Immunofluorescence against the indicated proteins were performed. Percentage of positive-cells were calculated after staining of the nucleus. E Ctrl n = 9, RSK3 = 9. F Ctrl n = 23, RSK3 n = 23. G Ctrl n = 10, RSK3 n = 19. Mann–Whitney test was used to determine statistical significance

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