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Fig. 1 | BMC Cancer

Fig. 1

From: uPAR enhances malignant potential of triple-negative breast cancer by directly interacting with uPA and IGF1R

Fig. 1

Co-overexpression of uPAS components and tumour-promoting proteins in TNBC samples and cell lines. a Immunohistochemical analysis of tumour samples showing positive expression and localisation of the proteins of interest: uPAR, uPA, PAI-1, IGF1R, IR and c-Met, bar: 50 μm and b Protein expressions of uPAR, uPA, PAI-1, IGF1R, IR and c-Met in the TNBC cohort (n = 174). c Immunoblottings of uPAR, uPA (supernatant), PAI-1, IGF1R, (phospho) c-Met, HER2, ER, PR in two TNBC cell lines: BT549 and MDA-MB-231 and in the breast cancer cell lines: BT474, MCF7, MDA-MB-361, SKBR3 and T47D. Tubulin was used as loading control

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