The sulfatase pathway as estrogen supply in endometrial cancer

•A novel method for a highly sensitive and accurate measurement of SULT1E1 activity is presented.•The sulfatase pathway is actively present in the endometrium and in EC.•STS seems the major route of intracellular estrogen supply in endometrial cells. Contradictory results are reported about the leve...

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Veröffentlicht in:Steroids 2018-11, Vol.139, p.45-52
Hauptverfasser: Cornel, K.M.C., Delvoux, B., Saya, T., Xanthoulea, S., Konings, G.F.J., Kruitwagen, R.P.F.M., Bongers, M.Y., Kooreman, L., Romano, A.
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Sprache:eng
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Zusammenfassung:•A novel method for a highly sensitive and accurate measurement of SULT1E1 activity is presented.•The sulfatase pathway is actively present in the endometrium and in EC.•STS seems the major route of intracellular estrogen supply in endometrial cells. Contradictory results are reported about the level of steroid sulfatase (STS), estrogen sulfotransferase (SULT1E1; together, the sulfatase pathway) and aromatase (CYP19A1) in endometrial cancer (EC). The aim of this study was to explore the levels of these enzymes in a well-characterized cohort of EC patients and postmenopausal controls. Endometrial tissues from 31 EC patients (21 grade 1 and 10 grade 2–3) and 19 postmenopausal controls were collected. Levels of mRNA (RT-qPCR) and protein (immunohistochemistry) were determined. STS enzyme activity was measured by HPLC, whereas SULT1E1 enzyme activity was determined using a novel method based on liquid chromatography-mass spectrometry (LC-MS/MS). No significant differences in STS, SULT1E1 mRNA or protein levels and STS:SULT1E1 ratio were found. STS enzyme activity and STS:SULT1E1 activity ratio were significantly decreased in ECs compared with controls. CYP19A1 mRNA levels were lower in ECs than in controls. A novel highly sensitive and accurate protocol to assess SULT1E1 activity is presented. STS enzyme activity and the STS:SULT1E1 activity ratio seem to be lower in ECs than in controls. STS is an important route for estrogen supply in endometrial cells.
ISSN:0039-128X
1878-5867
DOI:10.1016/j.steroids.2018.09.002