Retinoids, natural and synthetic vitamin A derivatives, are used as cancer chemo-preventive compounds. However, clinical trials have shown that retinoids can be deleterious leading to an increased incidence of neoplasias. The conflicting data regarding the pro/anti-oxidant potential of different retinoids molecules, stimulated us to investigate the effect of all-trans-Retinoic Acid (RA) on tumor cell proliferation in vitro. Dose-response treatment with RA at physiological doses promotes cell proliferation or autophagy while pharmacological doses results in apoptosis. RA is also implicated in a post-translation modification that modify the activity of the mitochondrial oxo-chetoglutarate carrier. Retinoids are often used as part of a combined therapy. We have elucidated the molecular mechanism by which treatment with rosiglitazone (BRL) and 9-cis-retinoic acid (9cRA) triggers apoptotic events in breast cancer cells as novel therapeutic tool for patients who develop resistance to anti-estrogen therapy. Recently 9cRA was found as endogenous in pancreas highlighted its rule in glucose stimulated insulin secretion mechanism and glucose homeostasis, establishing it as autocoid hormone.
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Retinoids, natural and synthetic vitamin A derivatives, are used as cancer chemo-preventive compounds. However, clinical trials have shown that retinoids can be deleterious leading to an increased incidence of neoplasias. The conflicting data regarding the pro/anti-oxidant potential of different retinoids molecules, stimulated us to investigate the effect of all-trans-Retinoic Acid (RA) on tumor cell proliferation in vitro. Dose-response treatment with RA at physiological doses promotes cell proliferation or autophagy while pharmacological doses results in apoptosis. RA is also implicated in a post-translation modification that modify the activity of the mitochondrial oxo-chetoglutarate carrier. Retinoids are often used as part of a combined therapy. We have elucidated the molecular mechanism by which treatment with rosiglitazone (BRL) and 9-cis-retinoic acid (9cRA) triggers apoptotic events in breast cancer cells as novel therapeutic tool for patients who develop resistance to anti-estrogen therapy. Recently 9cRA was found as endogenous in pancreas highlighted its rule in glucose stimulated insulin secretion mechanism and glucose homeostasis, establishing it as autocoid hormone.
Post-Doc at University of Calabria (Italy), she is PhD in Cellular Biochemistry and Drug Activity in Oncology. She has international collaborations with US and European Universities. One of the most successful areas pursued by the author has been the application of biochemical methods to study vitamin A derivatives effects in cancer and diabetes.
Les informations fournies dans la section « A propos du livre » peuvent faire référence à une autre édition de ce titre.
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Taschenbuch. Etat : Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Retinoids, natural and synthetic vitamin A derivatives, are used as cancer chemo-preventive compounds. However, clinical trials have shown that retinoids can be deleterious leading to an increased incidence of neoplasias. The conflicting data regarding the pro/anti-oxidant potential of different retinoids molecules, stimulated us to investigate the effect of all-trans-Retinoic Acid (RA) on tumor cell proliferation in vitro. Dose-response treatment with RA at physiological doses promotes cell proliferation or autophagy while pharmacological doses results in apoptosis. RA is also implicated in a post-translation modification that modify the activity of the mitochondrial oxo-chetoglutarate carrier. Retinoids are often used as part of a combined therapy. We have elucidated the molecular mechanism by which treatment with rosiglitazone (BRL) and 9-cis-retinoic acid (9cRA) triggers apoptotic events in breast cancer cells as novel therapeutic tool for patients who develop resistance to anti-estrogen therapy. Recently 9cRA was found as endogenous in pancreas highlighted its rule in glucose stimulated insulin secretion mechanism and glucose homeostasis, establishing it as autocoid hormone. 92 pp. Englisch. N° de réf. du vendeur 9783659580826
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Etat : New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Perri MariaritaPost-Doc at University of Calabria (Italy), she is PhD in Cellular Biochemistry and Drug Activity in Oncology. She has international collaborations with US and European Universities. One of the most successful areas pu. N° de réf. du vendeur 5166310
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Taschenbuch. Etat : Neu. This item is printed on demand - Print on Demand Titel. Neuware -Retinoids, natural and synthetic vitamin A derivatives, are used as cancer chemo-preventive compounds. However, clinical trials have shown that retinoids can be deleterious leading to an increased incidence of neoplasias. The conflicting data regarding the pro/anti-oxidant potential of different retinoids molecules, stimulated us to investigate the effect of all-trans-Retinoic Acid (RA) on tumor cell proliferation in vitro. Dose-response treatment with RA at physiological doses promotes cell proliferation or autophagy while pharmacological doses results in apoptosis. RA is also implicated in a post-translation modification that modify the activity of the mitochondrial oxo-chetoglutarate carrier. Retinoids are often used as part of a combined therapy. We have elucidated the molecular mechanism by which treatment with rosiglitazone (BRL) and 9-cis-retinoic acid (9cRA) triggers apoptotic events in breast cancer cells as novel therapeutic tool for patients who develop resistance to anti-estrogen therapy. Recently 9cRA was found as endogenous in pancreas highlighted its rule in glucose stimulated insulin secretion mechanism and glucose homeostasis, establishing it as autocoid hormone.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 92 pp. Englisch. N° de réf. du vendeur 9783659580826
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Taschenbuch. Etat : Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Retinoids, natural and synthetic vitamin A derivatives, are used as cancer chemo-preventive compounds. However, clinical trials have shown that retinoids can be deleterious leading to an increased incidence of neoplasias. The conflicting data regarding the pro/anti-oxidant potential of different retinoids molecules, stimulated us to investigate the effect of all-trans-Retinoic Acid (RA) on tumor cell proliferation in vitro. Dose-response treatment with RA at physiological doses promotes cell proliferation or autophagy while pharmacological doses results in apoptosis. RA is also implicated in a post-translation modification that modify the activity of the mitochondrial oxo-chetoglutarate carrier. Retinoids are often used as part of a combined therapy. We have elucidated the molecular mechanism by which treatment with rosiglitazone (BRL) and 9-cis-retinoic acid (9cRA) triggers apoptotic events in breast cancer cells as novel therapeutic tool for patients who develop resistance to anti-estrogen therapy. Recently 9cRA was found as endogenous in pancreas highlighted its rule in glucose stimulated insulin secretion mechanism and glucose homeostasis, establishing it as autocoid hormone. N° de réf. du vendeur 9783659580826
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Taschenbuch. Etat : Neu. Dynamic effects of Retinoic Acid isomers on cancer and physiology | Mariarita Perri (u. a.) | Taschenbuch | 92 S. | Englisch | 2014 | LAP LAMBERT Academic Publishing | EAN 9783659580826 | Verantwortliche Person für die EU: BoD - Books on Demand, In de Tarpen 42, 22848 Norderstedt, info[at]bod[dot]de | Anbieter: preigu. N° de réf. du vendeur 105168170
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