Razoxane and Dexrazoxane - Two Multifunctional Agents: Experimental and Clinical Results

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9789048191673: Razoxane and Dexrazoxane - Two Multifunctional Agents: Experimental and Clinical Results

Razoxane and dexrazoxane are two novel drugs with some uniquely useful features. They block cell division at the G2/M border, but nowhere else, so that they have a low toxicity profile. They suppress tumor metastasis and haemorrhages through normalization of pathological blood vessels. Razoxane potentiates radiotherapy especially in the treatment of soft tissue sarcomas and gastrointestinal neoplasms. They protect normal tissues against toxic chemicals, e.g. the myocardium against anthracyclines or subcutaneous tissue against injuries caused by incidental extravasations of anthracyclines. Dexrazoxane is the only drug approved by the FDA/EMEA for the specific purpose of preventing cardiac damage when giving the widely used and effective antitumor anthracyclines. The reduction of cardiotoxicity is achieved without response reduction or reducing of time to progression of tumors. While the full analysis of their actions at the molecular level is not yet completely understood, it seems most likely that it is via an inhibition on the topoisomerase II a. Moreover, the drugs have the ability to chelate several metals including iron, copper or zinc. The protection of normal tissues is nowhere more important than that of brain, and there are indications that the proteins thought to be responsible for the ravages of Alzheimer´s disease could be stabilized by one or both these drugs.

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Editorial: Springer, Netherlands (2010)
ISBN 10: 904819167X ISBN 13: 9789048191673
Nuevos Tapa dura Cantidad: 1
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The Book Depository
(London, Reino Unido)
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Descripción Springer, Netherlands, 2010. Hardback. Estado de conservación: New. 2011 ed.. Language: English . Brand New Book. Razoxane and dexrazoxane are two novel drugs with some uniquely useful features. They block cell division at the G2/M border, but nowhere else, so that they have a low toxicity profile. They suppress tumor metastasis and haemorrhages through normalization of pathological blood vessels. Razoxane potentiates radiotherapy especially in the treatment of soft tissue sarcomas and gastrointestinal neoplasms. They protect normal tissues against toxic chemicals, e.g. the myocardium against anthracyclines or subcutaneous tissue against injuries caused by incidental extravasations of anthracyclines. Dexrazoxane is the only drug approved by the FDA/EMEA for the specific purpose of preventing cardiac damage when giving the widely used and effective antitumor anthracyclines. The reduction of cardiotoxicity is achieved without response reduction or reducing of time to progression of tumors. While the full analysis of their actions at the molecular level is not yet completely understood, it seems most likely that it is via an inhibition on the topoisomerase II a. Moreover, the drugs have the ability to chelate several metals including iron, copper or zinc. The protection of normal tissues is nowhere more important than that of brain, and there are indications that the proteins thought to be responsible for the ravages of Alzheimer s disease could be stabilized by one or both these drugs. Nº de ref. de la librería LIB9789048191673

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Editorial: Springer, Netherlands (2010)
ISBN 10: 904819167X ISBN 13: 9789048191673
Nuevos Tapa dura Cantidad: 1
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The Book Depository US
(London, Reino Unido)
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Descripción Springer, Netherlands, 2010. Hardback. Estado de conservación: New. 2011 ed.. Language: English . Brand New Book. Razoxane and dexrazoxane are two novel drugs with some uniquely useful features. They block cell division at the G2/M border, but nowhere else, so that they have a low toxicity profile. They suppress tumor metastasis and haemorrhages through normalization of pathological blood vessels. Razoxane potentiates radiotherapy especially in the treatment of soft tissue sarcomas and gastrointestinal neoplasms. They protect normal tissues against toxic chemicals, e.g. the myocardium against anthracyclines or subcutaneous tissue against injuries caused by incidental extravasations of anthracyclines. Dexrazoxane is the only drug approved by the FDA/EMEA for the specific purpose of preventing cardiac damage when giving the widely used and effective antitumor anthracyclines. The reduction of cardiotoxicity is achieved without response reduction or reducing of time to progression of tumors. While the full analysis of their actions at the molecular level is not yet completely understood, it seems most likely that it is via an inhibition on the topoisomerase II a. Moreover, the drugs have the ability to chelate several metals including iron, copper or zinc. The protection of normal tissues is nowhere more important than that of brain, and there are indications that the proteins thought to be responsible for the ravages of Alzheimer s disease could be stabilized by one or both these drugs. Nº de ref. de la librería LIB9789048191673

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WALTER RHOMBERG
Editorial: Springer (2010)
ISBN 10: 904819167X ISBN 13: 9789048191673
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Herb Tandree Philosophy Books
(Stroud, GLOS, Reino Unido)
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Descripción Springer, 2010. Hardback. Estado de conservación: NEW. 9789048191673 This listing is a new book, a title currently in-print which we order directly and immediately from the publisher. Nº de ref. de la librería HTANDREE0389395

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Walter Rhomberg (editor), Kurt Hellmann (editor)
Editorial: Springer Netherlands 2010-10-06, Dordrecht (2010)
ISBN 10: 904819167X ISBN 13: 9789048191673
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Blackwell's
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Descripción Springer Netherlands 2010-10-06, Dordrecht, 2010. hardback. Estado de conservación: New. Nº de ref. de la librería 9789048191673

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Kurt Hellmann
Editorial: Springer-Verlag Gmbh Okt 2010 (2010)
ISBN 10: 904819167X ISBN 13: 9789048191673
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Valoración
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Descripción Springer-Verlag Gmbh Okt 2010, 2010. Buch. Estado de conservación: Neu. Neuware - Razoxane and dexrazoxane are two novel drugs with some uniquely useful features. They block cell division at the G2/M border, but nowhere else, so that they have a low toxicity profile. They suppress tumor metastasis and haemorrhages through normalization of patho-logical blood vessels. Razoxane potentiates radiotherapy especially in the treatment of soft tissue sarcomas and gastrointestinal neoplasms. They protect normal tissues against toxic chemicals, e.g. the myocardium against anthra-cyclines or subcutaneous tissue against injuries caused by incidental extravasations of anthra-cyclines. Dexrazoxane is the only drug approved by the FDA/UMEA for the specific purpose of preventing cardiac damage when giving the widely used and effective antitumor anthra-cyclines. The reduction of cardiotoxicity is achieved without response reduction or reducing of time to progression of tumors. While the full analysis of their actions at the molecular level is not yet completely understood, it seems most likely that it is via an inhibition on the topo-isomerase II a. Moreover, the drugs have the ability to chelate several metals including iron, copper or zinc. The protection of normal tissues is nowhere more important than that of brain, and there are indications that the proteins thought to be responsible for the ravages of Alzheimer s disease could be stabilized by one or both these drugs. 243 pp. Englisch. Nº de ref. de la librería 9789048191673

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Kurt Hellmann
Editorial: Springer-Verlag Gmbh Okt 2010 (2010)
ISBN 10: 904819167X ISBN 13: 9789048191673
Nuevos Cantidad: 1
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Rheinberg-Buch
(Bergisch Gladbach, Alemania)
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Descripción Springer-Verlag Gmbh Okt 2010, 2010. Buch. Estado de conservación: Neu. Neuware - Razoxane and dexrazoxane are two novel drugs with some uniquely useful features. They block cell division at the G2/M border, but nowhere else, so that they have a low toxicity profile. They suppress tumor metastasis and haemorrhages through normalization of patho-logical blood vessels. Razoxane potentiates radiotherapy especially in the treatment of soft tissue sarcomas and gastrointestinal neoplasms. They protect normal tissues against toxic chemicals, e.g. the myocardium against anthra-cyclines or subcutaneous tissue against injuries caused by incidental extravasations of anthra-cyclines. Dexrazoxane is the only drug approved by the FDA/UMEA for the specific purpose of preventing cardiac damage when giving the widely used and effective antitumor anthra-cyclines. The reduction of cardiotoxicity is achieved without response reduction or reducing of time to progression of tumors. While the full analysis of their actions at the molecular level is not yet completely understood, it seems most likely that it is via an inhibition on the topo-isomerase II a. Moreover, the drugs have the ability to chelate several metals including iron, copper or zinc. The protection of normal tissues is nowhere more important than that of brain, and there are indications that the proteins thought to be responsible for the ravages of Alzheimer s disease could be stabilized by one or both these drugs. 243 pp. Englisch. Nº de ref. de la librería 9789048191673

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7.

Kurt Hellmann
Editorial: Springer-Verlag Gmbh Okt 2010 (2010)
ISBN 10: 904819167X ISBN 13: 9789048191673
Nuevos Cantidad: 1
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Agrios-Buch
(Bergisch Gladbach, Alemania)
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Descripción Springer-Verlag Gmbh Okt 2010, 2010. Buch. Estado de conservación: Neu. Neuware - Razoxane and dexrazoxane are two novel drugs with some uniquely useful features. They block cell division at the G2/M border, but nowhere else, so that they have a low toxicity profile. They suppress tumor metastasis and haemorrhages through normalization of patho-logical blood vessels. Razoxane potentiates radiotherapy especially in the treatment of soft tissue sarcomas and gastrointestinal neoplasms. They protect normal tissues against toxic chemicals, e.g. the myocardium against anthra-cyclines or subcutaneous tissue against injuries caused by incidental extravasations of anthra-cyclines. Dexrazoxane is the only drug approved by the FDA/UMEA for the specific purpose of preventing cardiac damage when giving the widely used and effective antitumor anthra-cyclines. The reduction of cardiotoxicity is achieved without response reduction or reducing of time to progression of tumors. While the full analysis of their actions at the molecular level is not yet completely understood, it seems most likely that it is via an inhibition on the topo-isomerase II a. Moreover, the drugs have the ability to chelate several metals including iron, copper or zinc. The protection of normal tissues is nowhere more important than that of brain, and there are indications that the proteins thought to be responsible for the ravages of Alzheimer s disease could be stabilized by one or both these drugs. 243 pp. Englisch. Nº de ref. de la librería 9789048191673

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8.

Walter Rhomberg (Editor), Kurt Hellmann (Editor)
Editorial: Springer (2010)
ISBN 10: 904819167X ISBN 13: 9789048191673
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Ergodebooks
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Descripción Springer, 2010. Hardcover. Estado de conservación: New. 2011. This item is printed on demand. Nº de ref. de la librería DADAX904819167X

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Editorial: Springer (2010)
ISBN 10: 904819167X ISBN 13: 9789048191673
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Irish Booksellers
(Rumford, ME, Estados Unidos de America)
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Descripción Springer, 2010. Hardcover. Estado de conservación: New. book. Nº de ref. de la librería M904819167X

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Kurt Hellmann
Editorial: Springer-Verlag Gmbh Okt 2010 (2010)
ISBN 10: 904819167X ISBN 13: 9789048191673
Nuevos Cantidad: 1
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AHA-BUCH GmbH
(Einbeck, Alemania)
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Descripción Springer-Verlag Gmbh Okt 2010, 2010. Buch. Estado de conservación: Neu. Neuware - Razoxane and dexrazoxane are two novel drugs with some uniquely useful features. They block cell division at the G2/M border, but nowhere else, so that they have a low toxicity profile. They suppress tumor metastasis and haemorrhages through normalization of patho-logical blood vessels. Razoxane potentiates radiotherapy especially in the treatment of soft tissue sarcomas and gastrointestinal neoplasms. They protect normal tissues against toxic chemicals, e.g. the myocardium against anthra-cyclines or subcutaneous tissue against injuries caused by incidental extravasations of anthra-cyclines. Dexrazoxane is the only drug approved by the FDA/UMEA for the specific purpose of preventing cardiac damage when giving the widely used and effective antitumor anthra-cyclines. The reduction of cardiotoxicity is achieved without response reduction or reducing of time to progression of tumors. While the full analysis of their actions at the molecular level is not yet completely understood, it seems most likely that it is via an inhibition on the topo-isomerase II a. Moreover, the drugs have the ability to chelate several metals including iron, copper or zinc. The protection of normal tissues is nowhere more important than that of brain, and there are indications that the proteins thought to be responsible for the ravages of Alzheimer s disease could be stabilized by one or both these drugs. 243 pp. Englisch. Nº de ref. de la librería 9789048191673

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