Expression of sphingosine 1-phosphate receptor 4 and sphingosine kinase 1 is associated with outcome in oestrogen receptor-negative breast cancer

J. Ohotski, J. S. Long, C. Orange, B. Elsberger, E. Mallon, J. Doughty, S. Pyne, N. J. Pyne, J. Edwards (Lead / Corresponding author)

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    BACKGROUND: We previously reported that sphingosine 1-phosphate receptor 4 (S1P(4)) is expressed and stimulates the ERK-1/2 pathway via a human epidermal growth factor receptor 2 (HER2)-dependent mechanism in oestrogen receptor-negative (ER-) MDA-MB-453 breast cancer cells.

    METHODS: Clinical relevance of S1P(4) and sphingosine kinase 1 (SK1, which catalyses the formation of S1P) was assessed in a cohort of 140 ER- breast tumours by immunohistochemistry (IHC) and the weighted histoscore method. Additional evidence for a functional interaction between S1P(4) and SK1 and between HER2 and SK1 was obtained using MDA-MB-453 cells.

    RESULTS: High S1P(4) expression is associated with shorter disease-free (P = 0.014) and disease-specific survival (P = 0.004), and was independent on multivariate analysis. In addition, patients with tumours that contain high and low levels of SK1 and S1P(4), respectively, have a significantly shorter disease-free survival (P = 0.043) and disease-specific survival (P = 0.033) compared with patients whose tumours contain both low S1P(4) and SK1 levels. In addition, high tumour expression of SK1 was significantly associated with shorter disease-specific survival (P = 0.0001) in patients with HER2-positive tumours. Treatment of MDA-MB-453 cells with the SK1 inhibitor, SKi (2-(p-hydroxyanilino)-4-(p-chlorophenyl) thiazole) reduced the basal and S1P/S1P(4)-induced activation of ERK-1/2 and altered HER2 trafficking in these cells.

    CONCLUSION: These findings highlight an important role for S1P(4) and SK1 in ER- breast cancer progression. British Journal of Cancer (2012) 106, 1453-1459. doi: 10.1038/bjc.2012.98 Published online 29 March 2012 (C) 2012 Cancer Research UK

    Original languageEnglish
    Pages (from-to)1453-1459
    Number of pages7
    JournalBritish Journal of Cancer
    Issue number8
    Publication statusPublished - 10 Apr 2012

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