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Distinct modulation of alkaline phosphatase isoenzymes by 17 beta-estradiol and xanthohumol in breast cancer MCF-7 cells

Title
Distinct modulation of alkaline phosphatase isoenzymes by 17 beta-estradiol and xanthohumol in breast cancer MCF-7 cells
Type
Article in International Scientific Journal
Year
2007
Authors
Susana Guerreiro
(Author)
Other
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Rosario Monteiro
(Author)
FCNAUP
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Maria Joao Martins
(Author)
FMUP
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Conceicao Calhau
(Author)
FMUP
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Isabel Azevedo
(Author)
Other
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Raquel Soares
(Author)
FMUP
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Journal
Title: Clinical BiochemistryImported from Authenticus Search for Journal Publications
Vol. 40
Pages: 268-273
ISSN: 0009-9120
Publisher: Elsevier
Scientific classification
FOS: Engineering and technology > Medical engineering
Other information
Authenticus ID: P-004-BY9
Abstract (EN): Objectives: To examine the effect of 17 beta-estradiol and xanthohumol in alkaline phosphatase (ALP) expression and activity in breast cancer MCF-7 cells. Design and methods: ALP isoenzytnes expression was evaluated by RT-PCR and Western blotting. ALP activity was measured by spectrophotometry. Cell proliferation and apoptosis were examined by MTT and immunostaining for K167 and TUNEL, respectively. Results: ALP isoenzymes expression and activity were decreased by 1 nM 17 beta-estradiol. Pure estrogenic antagonist (ICI 182,780) reversed 17 beta-estradiol-inhibiting effect in TNS-ALP expression. RNA and protein expression of IALP, but not TNS-ALP, was also decreased by incubation with 10 mu M xanthohumol (IC50) and was accompanied by a significant reduction in ALP activity. Treatment with 17 beta-estradiol enhanced cell proliferation and decreased apoptosis. Conversely, xanthohumol incubation inhibited cell viability and apoptosis. Conclusion: Estrogens and xanthohumol differently modulate ALP isoenzymes. ALP loss associated with increased cell proliferation. Modulation of this enzyme by 17 beta-estradiol and xanthohumol might provide therapeutic strategies against hormone-dependent breast cancer.
Language: English
Type (Professor's evaluation): Scientific
Contact: raqsoa@med.up.pt
No. of pages: 6
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