Leptin induces upregulation of sphingosine kinase 1 in oestrogen receptor-negative breast cancer via Src family kinase-mediated, janus kinase 2-independent pathway

被引:38
作者
Alshaker, Heba [1 ,2 ]
Krell, Jonathan [1 ]
Frampton, Adam E. [1 ]
Waxman, Jonathan [1 ]
Blyuss, Oleg [3 ]
Zaikin, Alexey [3 ]
Winkler, Mathias [1 ]
Stebbing, Justin [1 ]
Yaguee, Ernesto [1 ]
Pchejetski, Dmitri [4 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Hammersmith Hosp, Dept Surg & Canc, London W12 0NN, England
[2] Petra Univ, Fac Pharm & Med Sci, Dept Pharmacol & Biomed Sci, Amman, Jordan
[3] UCL, Inst Womens Hlth, London WC1E 6AU, England
[4] Univ E Anglia, Sch Med, Norwich NR4 7TJ, Norfolk, England
关键词
PROSTATE-CANCER; SIGNALING PATHWAYS; MESSENGER-RNA; EXPRESSION; CELL; OBESITY; ACTIVATION; INHIBITION; 1-PHOSPHATE; PROTEIN;
D O I
10.1186/s13058-014-0426-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Introduction: Obesity is a known risk factor for breast cancer. Sphingosine kinase 1 (SK1) is an oncogenic lipid kinase that is overexpressed in breast tumours and linked with poor prognosis, however, its role in obesity-driven breast cancer was never elucidated. Methods: Human primary and secondary breast cancer tissues were analysed for SK1 and leptin receptor expression using quantitative real-time polymerase chain reaction (qRT-PCR) assay. Leptin-induced signalling was analysed in human oestrogen receptor (ER)-positive and negative breast cancer cells using Western blotting, qRT-PCR and radiolabelling assays. Results: Our findings show for the first time that human primary breast tumours and associated lymph node metastases exhibit a strong correlation between SK1 and leptin receptor expression (Pearson R = 0.78 and R = 0.77, respectively, P < 0.001). Both these genes are elevated in metastases of ER-negative patients and show a significant increase in patients with higher body mass index (BMI). Leptin induces SK1 expression and activation in ER-negative breast cancer cell lines MDAMB-231 and BT-549, but not in ER-positive cell lines. Pharmacological inhibition and gene knockdown showed that leptin-induced SK1 activity and expression are mediated by activation of extracellular signal-regulated kinases 1/2 (ERK1/2) and Src family kinase (SFK) pathways, but not by the major pathways downstream of leptin receptor (LEPR) - janus kinase 2 (JAK2) and signal transducer and activator of transcription 3 (STAT3). Src-homology 2 domain-containing phosphatase 2 (SHP2) appeared to be key to SK1 activation, and may function as an adaptor protein between SFKs and LEPR. Importantly, leptin-induced breast cancer cell proliferation was abrogated by SK1-specific small interfering RNA (siRNA). Conclusions: Overall, our findings demonstrate a novel SFK/ERK1/2-mediated pathway that links leptin signalling and expression of oncogenic enzyme SK1 in breast tumours and suggest the potential significance of this pathway in ER-negative breast cancer.
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页数:15
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