Fr. 239.00

Deoxynucleoside Analogs in Cancer Therapy

Inglese · Tascabile

Spedizione di solito entro 6 a 7 settimane

Descrizione

Ulteriori informazioni

Successful cancer chemotherapy relies heavily on the application of various deoxynucleoside analogs. Since the very beginning of modern cancer chemotherapy, a number of antimetabolites have been introduced into the clinic and subsequently applied widely for the treatment of many malignancies, both solid tumors and hematological disorders. In the latter diseases, cytarabine has been the mainstay of treatment of acute myeloid leukemia. Although many novel compounds were synthesized in the 1980s and 1990s, no real improvement was made. However, novel technology is now capable of elucidating the molecular basis of several inborn errors as well as some specific malignancies. This has enabled the synthesis of several deoxynucleoside analogs that could be applied for specific malignancies, such as pentostatin and subsequently chlorodeoxyadenosine (cladribine) for the treatment of hairy cell leukemia. Already in the early stage of deoxynucleoside analog development, it was recognized that several of these compounds were very effective in the treatment of various viral infections, such as for the treatment of herpes infections. This formed the basis initially for the design of azidothymidine and subsequently many other analogs, which are currently successfully used for the treatment of HIV infections. As a spin-off of these research lines, some compounds not eligible for development as antiviral agents appeared to be very potent anticancer agents. The classical example is gemcitabine, now one of the most widely applied deoxynucleoside analogs, used for the (combination) treatment of non-small cell lung cancer, pancreatic cancer, bladder cancer, and ovarian cancer.

Sommario

Nucleoside Transport Into Cells.- The Role of Deoxycytidine Kinase in DNA Synthesis and Nucleoside Analog Activation.- Deoxynucleoside Kinases and Their Potential Role in Deoxynucleoside Cytotoxicity.- Nucleotidases and Nucleoside Analog Cytotoxicity.- Pumping Out Drugs.- Cytosine Arabinoside.- Clofarabine.- L-Nucleosides as Chemotherapeutic Agents.- Troxacitabine (Troxatyl (TM)).- 9-?-D-Arabinofuranosylguanine.- Gemcitabine.- Clinical Activity of Gemcitabine as a Single Agent and in Combination.- Nucleoside Radiosensitizers.- NONMEM Population Models of Cytosine Arabinoside and Fludarabine Phosphate in Pediatric Patients With Leukemia.- ThecycloSal-Nucleotide Delivery System.- Purine and Pyrimidine-Based Analogs and Suicide Gene Therapy.- 3?-Deoxy-3?-Fluorothymidine as a Tracer of Proliferation in Positron Emission Tomography.

Riassunto

Successful cancer chemotherapy relies heavily on the application of various deoxynucleoside analogs. Since the very beginning of modern cancer chemotherapy, a number of antimetabolites have been introduced into the clinic and subsequently applied widely for the treatment of many malignancies, both solid tumors and hematological disorders. In the latter diseases, cytarabine has been the mainstay of treatment of acute myeloid leukemia. Although many novel compounds were synthesized in the 1980s and 1990s, no real improvement was made. However, novel technology is now capable of elucidating the molecular basis of several inborn errors as well as some specific malignancies. This has enabled the synthesis of several deoxynucleoside analogs that could be applied for specific malignancies, such as pentostatin and subsequently chlorodeoxyadenosine (cladribine) for the treatment of hairy cell leukemia. Already in the early stage of deoxynucleoside analog development, it was recognized that several of these compounds were very effective in the treatment of various viral infections, such as for the treatment of herpes infections. This formed the basis initially for the design of azidothymidine and subsequently many other analogs, which are currently successfully used for the treatment of HIV infections. As a spin-off of these research lines, some compounds not eligible for development as antiviral agents appeared to be very potent anticancer agents. The classical example is gemcitabine, now one of the most widely applied deoxynucleoside analogs, used for the (combination) treatment of non-small cell lung cancer, pancreatic cancer, bladder cancer, and ovarian cancer.

Testo aggiuntivo

"...a top-notch overview of the current knowledge in the area of deoxynucleoside analog development and application in the treatment of cancer."  -Weighted Numerical Score: 92 - 4 Stars!-Doody's Health Science Book Review Journal
 
"...an excellent book that is suitable for researchers or clinicians with an interest in deoxynucleoside analgos and/or cancer chemotherapy."  -Weighted Numerical Score: 92 - 4 Stars!-Doody's Health Science Book Review Journal

Relazione

"...a top-notch overview of the current knowledge in the area of deoxynucleoside analog development and application in the treatment of cancer."  -Weighted Numerical Score: 92 - 4 Stars!-Doody's Health Science Book Review Journal
 
"...an excellent book that is suitable for researchers or clinicians with an interest in deoxynucleoside analgos and/or cancer chemotherapy."  -Weighted Numerical Score: 92 - 4 Stars!-Doody's Health Science Book Review Journal

Dettagli sul prodotto

Con la collaborazione di Godefridu J Peters (Editore), Godefridus J Peters (Editore), Godefridus J Peters (Editore), Godefridus J. Peters (Editore)
Editore Springer, Berlin
 
Lingue Inglese
Formato Tascabile
Pubblicazione 25.10.2010
 
EAN 9781617374975
ISBN 978-1-61737-497-5
Pagine 476
Dimensioni 170 mm x 230 mm x 27 mm
Peso 724 g
Illustrazioni XIV, 476 p.
Serie Cancer Drug Discovery and Development
Cancer Drug Discovery & Develo
Cancer Drug Discovery & Develo
Cancer Drug Discovery and Development
Categorie Scienze naturali, medicina, informatica, tecnica > Medicina > Branche non cliniche

C, Research, METABOLISM, Chemotherapy, Leukemia, Biomedical and Life Sciences, Cancer Research, Gene Therapy, Cancer Biology, drug discovery, pharmacokinetics, pancreatic cancer, drug, kinetics, oncogenes

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