Drug Discovery and Development for Advanced Melanoma
Details
Malignant melanoma is the most dangerous type of skin cancer. It accounts for about 75% of skin cancer deaths. Patients with advanced melanoma with dissemination to distant sites and visceral organs have a very poor prognosis, with a median survival time of 6 months and a 5-year survival rate of less than 5%. Over the past 40 years, no one drug or combination of drugs demonstrated any improvement on survival of metastatic melanoma patient. In the year 2011, FDA approved ipilimumab and Vemurafenib for the treatment of advanced melanoma. But both drugs only prolonged patients life of 2-3 months. So the war to fight advanced melanoma is far from ending. In this book, the author and colleagues used classical approaches discovering and developing novel therapeutic agents for advanced melanoma. They identified several new classes of compounds which showed very potent in vitro activity against metastatic melanoma cells and in vivo activity on several animal models. They further optimized the lead compounds activity through a knowledge-based molecule design. They also identified the cellular target of these compounds and elucidated their mechanism of action in killing melanoma cells.
Autorentext
Zhao Wang, born in 1975, received his Bachelor of Medicine degree from the Shandong University in 2000. He received his Master of Pharmaceutical Sciences degree from the Peking Union Medical College (PUMC) in 2003. In 2010, he received his Ph.D. in Pharmaceutical Sciences from the University of Tennessee under the supervision of Prof. Wei Li.
Weitere Informationen
- Allgemeine Informationen
- Sprache Englisch
- Autor Zhao Wang
- Titel Drug Discovery and Development for Advanced Melanoma
- ISBN 978-3-8465-2070-3
- Format Kartonierter Einband (Kt)
- EAN 9783846520703
- Jahr 2011
- Größe H220mm x B150mm x T11mm
- Untertitel From lead compounds identification, optimization to in vivo anti-melanoma efficacy testing on animal models
- Gewicht 296g
- Auflage Aufl.
- Genre Medizin
- Anzahl Seiten 188
- Herausgeber LAP Lambert Acad. Publ.
- GTIN 09783846520703