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Fig. 1 | Molecular Cancer

Fig. 1

From: Syndecan-1 is a novel molecular marker for triple negative inflammatory breast cancer and modulates the cancer stem cell phenotype via the IL-6/STAT3, Notch and EGFR signaling pathways

Fig. 1

Expression of Syndecan-1 and the CSC marker CD44 in carcinoma tissues of IBC vs non-IBC patients, SUM-149 and SKBR3 cells. a Higher expression of Syndecan-1 mRNA level in carcinoma tissues of IBC (n = 13) vs non-IBC (n = 14). RQ values of mRNA expression are log2-transformed and normalized to values of normal tissues collected during reduction mammoplasty. Bars represent median with interquartile range. ** P < 0.01 as determined by Mann-Whitney U-test. b Representative fields of immunostaining (brown color) of Syndecan-1 and CD44 in paraffin embedded carcinoma tissue sections of triple negative IBC (n = 13) and non-IBC (n = 17) patients. A high density of cancer cells positive for CD44 and Syndecan-1 is observed in IBC vs non-IBC. c Pearson’s correlation between Syndecan-1 and CD44 expression in carcinoma tissues of IBC vs non-IBC. d A representative flow cytometric analysis for the expression of CD44 and Syndecan-1 in SUM-149 and SKBR3 cells. e Quantitative analysis of four subpopulations; CD44(-)Syndecan-1(-), CD44(+)Syndecan-1(-), CD44(-)Syndecan-1(+) and CD44(+)Syndecan-1(+). Syndecan-1 is higher expressed in the CD44(+)-enriched subset in SUM-149 cells than that in SKBR3 cells. Data represent mean ± SEM, n ≥ 3. ** P < 0.01, # P < 0.001 as determined by Student’s t-test. Data shown are a single experiment representative of three independent experiments

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