Cited by 33Ovarian cancer diagnosis and treatmentEstrogen and related hormone effectsOvarian function and disorders

Clinical significance of the estrogen-modifying enzymes steroid sulfatase and estrogen sulfotransferase in epithelial ovarian cancer

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Mungenast, Felicitas, Aust, Stefanie, Vergote, Ignace, Vanderstichele, Adriaan, Sehouli, Jalid, Braicu, Elena, Mahner, Sven, Castillo-Tong, Dan Cacsire +2 more·2017·Oncology Letters

Abstract

17β-estradiol (E2) can contribute to the progression of epithelial ovarian cancer (EOC). Although the majority of patients with EOC are postmenopausal woman, when de novo estrogen production in the ovary has ceased, ovarian cancer cells remain exposed to estrogens synthesized locally in the cancer cells from inactive sulfonated steroid hormone precursors-such as estrone sulfate taken up from the circulation via the sulfatase pathway. An abundance of the estrogen-modifying enzymes, including estrogen-activating steroid sulfatase (STS) and estrogen-inactivating estrogen-sulfotransferase (SULT1E1), is important for providing active estrogen to EOC cells. Therefore, the present study determined the levels of SULT1E1, STS and estrogen receptor α (ERα) protein in paraffin-embedded specimens from 206 patients with Federation of Gynecology and Obstetrics stage II-IV EOC treated with debulking surgery and standard platinum-based adjuvant chemotherapy. The levels of STS, SULT1E1 and ERα were assessed by automated quantitative microscopy-based image analysis subsequent to immunohistochemical staining. Significantly higher SULT1E1 levels were observed in better differentiated EOC tumors compared to grade 3 EOC tumors (P=0.001). STS and SULT1E1 levels were positively associated with ERα abundance (P<0.001 and P=0.001, respectively). In advanced stage high-grade serous EOC (HGSOC; n=132), the most frequent and lethal type of ovarian cancer, SULT1E1 expression was significantly associated with a better overall survival rate (hazard ratio 0.66, 95% confidence interval, 0.45-0.94; P=0.005). These results highlight the importance of SULT1E1-mediated estrogen inactivation in EOC, particularly HGSOC. Therefore, targeting the sulfatase pathway is a potential endocrine therapeutic intervention for certain patients with estrogen-responsive EOC.

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Authors
Mungenast, F., Aust, S., Vergote, I., Vanderstichele, A., Sehouli, J., Braicu, E., Mahner, S., Castillo-Tong, D. C., Zeillinger, R., & Thalhammer, T.
Affiliations
  • Medical University of Vienna (AT)
  • Comprehensive Cancer Center Vienna (AT)
  • KU Leuven (BE)
  • Charité – Universitätsmedizin Berlin (DE)
  • Ludwig-Maximilians-Universität München (DE)
Corresponding author
Thalhammer, Theresia
Venue
Oncology Letters
Published
2017-04-03
Volume
13
Issue
6
Pages
4047-4054
ISSN
  • 1792-1074 (ISSN-L)
  • 1792-1082
OpenAlex
W2604510558
Cited by
33
References
48
Citations by year
2026: 1 · 2025: 5 · 2024: 4 · 2023: 6 · 2022: 1 · 2021: 7 · 2020: 2 · 2019: 2 · 2018: 4 · 2017: 1
FWCI
2.85
Type
journal article
Language
en
Open access
Licence
cc-by-nc-nd
Locations
  • Oncology Letters (publishedVersion, cc-by-nc-nd)
  • Europe PMC (PubMed Central) (publishedVersion, other-oa)
  • PubMed Central (publishedVersion, cc-by-nc-nd)
  • PubMed (publishedVersion)
  • Lirias (submittedVersion, other-oa)
Funders
European Commission (018698)
Topics
  • Health Sciences › Medicine › Reproductive Medicine › Ovarian cancer diagnosis and treatment
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Estrogen and related hormone effects
  • Health Sciences › Medicine › Reproductive Medicine › Ovarian function and disorders
Keywords
epithelial ovarian cancer, steroid sulfatase, estrogen receptor alpha, estrone sulfate, estrogen metabolism, high-grade serous ovarian cancer, tumor differentiation, overall survival, endocrine therapy

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