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Expression of the forkhead transcription factor FOXL2 correlates with good prognosis in breast cancer patients treated with tamoxifen
Department of Clinical Medicine, School of Health and Medical Sciences, Örebro University, 701 85 Örebro, Sweden.
Department of Clinical Medicine, School of Health and Medical Sciences, Örebro University, 701 85 Örebro, Sweden.
University of Skövde, School of Life Sciences. University of Skövde, The Systems Biology Research Centre.
Department of Pathology, School of Health and Medical Sciences, Örebro University Hospital, 701 85 Örebro, Sweden.
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2011 (English)In: International Journal of Oncology, ISSN 1019-6439, Vol. 38, no 4, 1145-1151 p.Article in journal (Refereed) Published
Abstract [en]

Aromatase is an important enzyme in the local synthesis of oestrogens and its expression has been shown to be increased in breast cancer through the activation of multiple promoters. However, the mechanisms behind this are not yet fully understood. A novel candidate in this context is the transcription factor forkhead box L2 (FOXL2), which has been recognised to be co-expressed with aromatase and transcriptionally active promoter II in developing goat and chicken ovaries. We propose that FOXL2 could be involved in the increased expression of aromatase in breast cancer. We examined FOXL2 and its relation to aromatase in 132 post-menopausal breast cancer patients by immunohistochemistry. Using in silico analysis, we further searched for FOXL2 binding-elements in the aromatase gene promoters. The results demonstrate that FOXL2 is expressed in breast cancer and influences clinical outcome with improved recurrence-free survival in cases with nuclear expression. In a multivariate Cox model, nuclear FOXL2 was a significant prognostic factor in ER-positive patients treated with tamoxifen (HR=0.18, 95% confidence interval (CI)=0.04-0.81, P=0.03). Tumours expressing nuclear FOXL2 were also more likely positive for stromal and/or cytoplasmic aromatase (P=0.03 and P=0.008, respectively). In silico analyses revealed binding elements of FOXL2 in promoters I.3, II and I.7 of the aromatase gene of which promoter I.7 was most significant. In conclusion, this is the first study to report that FOXL2 is expressed in breast cancer and correlates with aromatase as well as with clinical outcome. The results further strengthen a possible binding of FOXL2 to aromatase promoter I.7. Nevertheless, whether FOXL2 is a direct activator of aromatase requires further investigation.

Place, publisher, year, edition, pages
Spandidos Publications Ltd. , 2011. Vol. 38, no 4, 1145-1151 p.
Keyword [en]
breast cancer, forkhead box L2, aromatase, tissue specific promoters, in silico
National Category
Natural Sciences
Research subject
Natural sciences
Identifiers
URN: urn:nbn:se:his:diva-5153DOI: 10.3892/ijo.2011.923ISI: 000288581100027PubMedID: 21271216Scopus ID: 2-s2.0-79952329924OAI: oai:DiVA.org:his-5153DiVA: diva2:427615
Available from: 2011-06-28 Created: 2011-06-28 Last updated: 2012-12-13Bibliographically approved

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