Estrogen and selective estrogen receptor modulators (SERMs) differentially impact endometrial and breast cancer cell function, however, the biological basis of these differences is not established. Deregulated cell adhesion to the extracellular matrix, cell movement and invasion are related to several disorders, such as endometriosis, endometrial and breast cancer metastasis. Remodeling of the actin cytoskeleton is required to achieve cell adhesion and movement. Estrogen receptor (ER) regulates actin and cell membrane remodeling through extra-nuclear signaling cascades. The aim of the present work was to characterize the effects of raloxifene, tamoxifen and 17?-estradiol on breast and endometrial cancer cells cytoskeletal remodeling, migration and invasion. These findings will increase our understanding of the actions of estrogen and SERMs in breast cancer and endometrial cells and will highlight potential molecular targets to interfere with the estrogen-related altered cell adhesion encountered in endometrial disorders or breast cancer progression and/or metastasis induced by estrogens in postmenopausal women.
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Estrogen and selective estrogen receptor modulators (SERMs) differentially impact endometrial and breast cancer cell function, however, the biological basis of these differences is not established. Deregulated cell adhesion to the extracellular matrix, cell movement and invasion are related to several disorders, such as endometriosis, endometrial and breast cancer metastasis. Remodeling of the actin cytoskeleton is required to achieve cell adhesion and movement. Estrogen receptor (ER) regulates actin and cell membrane remodeling through extra-nuclear signaling cascades. The aim of the present work was to characterize the effects of raloxifene, tamoxifen and 17?-estradiol on breast and endometrial cancer cells cytoskeletal remodeling, migration and invasion. These findings will increase our understanding of the actions of estrogen and SERMs in breast cancer and endometrial cells and will highlight potential molecular targets to interfere with the estrogen-related altered cell adhesion encountered in endometrial disorders or breast cancer progression and/or metastasis induced by estrogens in postmenopausal women.
Born in Argentina in 1980, she obtained her degree in Biology from Universidad Nacional del Sur, Bahia Blanca in 2004. In 2006 she was incorporated at Molecular and Cellular Gynecological Endocrinology Laboratory where she began to study endometrial and breast cancer. In 2010 she received the Ph.D. from Pisa University.
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Vendeur : BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, Allemagne
Taschenbuch. Etat : Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Estrogen and selective estrogen receptor modulators (SERMs) differentially impact endometrial and breast cancer cell function, however, the biological basis of these differences is not established. Deregulated cell adhesion to the extracellular matrix, cell movement and invasion are related to several disorders, such as endometriosis, endometrial and breast cancer metastasis. Remodeling of the actin cytoskeleton is required to achieve cell adhesion and movement. Estrogen receptor (ER) regulates actin and cell membrane remodeling through extra-nuclear signaling cascades. The aim of the present work was to characterize the effects of raloxifene, tamoxifen and 17 -estradiol on breast and endometrial cancer cells cytoskeletal remodeling, migration and invasion. These findings will increase our understanding of the actions of estrogen and SERMs in breast cancer and endometrial cells and will highlight potential molecular targets to interfere with the estrogen-related altered cell adhesion encountered in endometrial disorders or breast cancer progression and/or metastasis induced by estrogens in postmenopausal women. 64 pp. Englisch. N° de réf. du vendeur 9783838394480
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Etat : New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Flamini Marina InesBorn in Argentina in 1980, she obtained her degree in Biology from Universidad Nacional del Sur, Bahia Blanca in 2004. In 2006 she was incorporated at Molecular and Cellular Gynecological Endocrinology Laborator. N° de réf. du vendeur 5419672
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Taschenbuch. Etat : Neu. This item is printed on demand - Print on Demand Titel. Neuware -Estrogen and selective estrogen receptor modulators (SERMs) differentially impact endometrial and breast cancer cell function, however, the biological basis of these differences is not established. Deregulated cell adhesion to the extracellular matrix, cell movement and invasion are related to several disorders, such as endometriosis, endometrial and breast cancer metastasis. Remodeling of the actin cytoskeleton is required to achieve cell adhesion and movement. Estrogen receptor (ER) regulates actin and cell membrane remodeling through extra-nuclear signaling cascades. The aim of the present work was to characterize the effects of raloxifene, tamoxifen and 17ß-estradiol on breast and endometrial cancer cells cytoskeletal remodeling, migration and invasion. These findings will increase our understanding of the actions of estrogen and SERMs in breast cancer and endometrial cells and will highlight potential molecular targets to interfere with the estrogen-related altered cell adhesion encountered in endometrial disorders or breast cancer progression and/or metastasis induced by estrogens in postmenopausal women.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 64 pp. Englisch. N° de réf. du vendeur 9783838394480
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Vendeur : AHA-BUCH GmbH, Einbeck, Allemagne
Taschenbuch. Etat : Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Estrogen and selective estrogen receptor modulators (SERMs) differentially impact endometrial and breast cancer cell function, however, the biological basis of these differences is not established. Deregulated cell adhesion to the extracellular matrix, cell movement and invasion are related to several disorders, such as endometriosis, endometrial and breast cancer metastasis. Remodeling of the actin cytoskeleton is required to achieve cell adhesion and movement. Estrogen receptor (ER) regulates actin and cell membrane remodeling through extra-nuclear signaling cascades. The aim of the present work was to characterize the effects of raloxifene, tamoxifen and 17 -estradiol on breast and endometrial cancer cells cytoskeletal remodeling, migration and invasion. These findings will increase our understanding of the actions of estrogen and SERMs in breast cancer and endometrial cells and will highlight potential molecular targets to interfere with the estrogen-related altered cell adhesion encountered in endometrial disorders or breast cancer progression and/or metastasis induced by estrogens in postmenopausal women. N° de réf. du vendeur 9783838394480
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Taschenbuch. Etat : Neu. RAPID SIGNALING OF ESTROGEN RECEPTOR TO BREAST AND ENDOMETRIAL CANCER | Estrogen and SERMs possible rol in endometrial and breast metastasis | Marina Ines Flamini (u. a.) | Taschenbuch | 64 S. | Englisch | 2010 | LAP LAMBERT Academic Publishing | EAN 9783838394480 | Verantwortliche Person für die EU: BoD - Books on Demand, In de Tarpen 42, 22848 Norderstedt, info[at]bod[dot]de | Anbieter: preigu Print on Demand. N° de réf. du vendeur 107426357
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