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Schistosoma haematobium: Identification of new estrogenic molecules with estradiol antagonistic activity and ability to inactivate estrogen receptor in mammalian cells

Title
Schistosoma haematobium: Identification of new estrogenic molecules with estradiol antagonistic activity and ability to inactivate estrogen receptor in mammalian cells
Type
Article in International Scientific Journal
Year
2010
Authors
Monica Catarina Botelho
(Author)
Other
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Raquel Soares
(Author)
FMUP
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Ricardo Ribeiro
(Author)
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Vania Camilo
(Author)
Other
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Raquel Almeida
(Author)
FMUP
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Rui Medeiros
(Author)
ICBAS
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Jose Carlos Machado
(Author)
FMUP
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Jose Manuel C Correia da Costa
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Journal
Vol. 126 No. 4
Pages: 526-535
ISSN: 0014-4894
Publisher: Elsevier
Indexing
Scientific classification
FOS: Medical and Health sciences > Health sciences
Other information
Authenticus ID: P-003-0G7
Abstract (EN): We have previously identified the expression of an estradiol (E2)-related molecule by Schistosoma haematobium total antigen (Sh). We now show that this molecule has an antagonistic effect of estradiol in vitro. Our results are consistent with the existence of an estrogenic molecule that antagonizes the activity of estradiol. We found evidence for this molecule as we identified and characterized by mass spectrometry new estrogenic molecules previously unknown, present in schistosome worm extracts and sera of Schistosoma-infected individuals. We also show that Sh is able to interact in vitro with estrogen receptor (ER), explaining how host endocrine system can favor the establishment of schistosomes. These findings highlight the exploitation of the host endocrine system by schistosomes and represent an additional regulatory component of schistosome development that defines a novel paradigm enabling host-parasite interactions. The identification of these molecules opens new ways for the development of alternative drugs to treat schistosomiasis.
Language: English
Type (Professor's evaluation): Scientific
Contact: monicabotelho@hotmail.com
No. of pages: 10
License type: Click to view license CC BY-NC
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ART_54 526.04 KB
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