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BRAF Targets in Melanoma: Biological Mechanisms, Resistance, and Drug Discovery 2015 ed. [Hardback]

  • Formāts: Hardback, 204 pages, height x width: 235x155 mm, weight: 4439 g, 21 Illustrations, color; 5 Illustrations, black and white; VIII, 204 p. 26 illus., 21 illus. in color., 1 Hardback
  • Sērija : Cancer Drug Discovery and Development 82
  • Izdošanas datums: 25-Nov-2014
  • Izdevniecība: Humana Press Inc.
  • ISBN-10: 1493921428
  • ISBN-13: 9781493921423
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  • Hardback
  • Cena: 91,53 €*
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  • Formāts: Hardback, 204 pages, height x width: 235x155 mm, weight: 4439 g, 21 Illustrations, color; 5 Illustrations, black and white; VIII, 204 p. 26 illus., 21 illus. in color., 1 Hardback
  • Sērija : Cancer Drug Discovery and Development 82
  • Izdošanas datums: 25-Nov-2014
  • Izdevniecība: Humana Press Inc.
  • ISBN-10: 1493921428
  • ISBN-13: 9781493921423
Citas grāmatas par šo tēmu:
?This volume contains a collection of writings from the leaders in the fields of Molecular Biology and Melanoma Research which will begin to tell the ever-expanding story of the most recent findings, discoveries, and potential of BRAF-directed targets in melanoma. Recent research has shown that BRAF inhibitors are effective for a short period of time, but there is little hope that this drugs as single agents will lead to durable benefit in a majority of patients. Among scientists and researchers who work in drug discovery, there is a lot of interest in the development of molecularly targeted cancer agents. Namely, the identification of a molecular target, the selection of molecules which effectively inhibit this target. What is starkly different about the development of this class of compounds, however, is that the mechanism of action of these agents are not as straightforward as was once previously assumed and the mechanisms of resistance that tumor cells employ to evade complete destruction are unlike any that have been described before. These discoveries in addition to utilization of modern molecular biology techniques have led to a series of hypotheses regarding which other types of molecules could be used in combination with BRAF-inhibitors in hopes of revolutionizing the potential of therapeutics in melanoma.
1 Melanoma: Historical Context
1(24)
Suraj Venna
Sekwon Jang
Michael Atkins
2 Melanoma Pathogenesis
25(22)
Jennifer A. Lo
David E. Fisher
3 Molecular Diagnostics and Tumor Mutational Analysis
47(20)
Melissa A. Wilson
Katherine L. Nathanson
4 Clinical Utility of BRAF-Targeted Therapy in Melanoma
67(18)
Jeffrey A. Sosman
Douglas B. Johnson
5 The Ethics of Randomized Trials in Oncology
85(20)
Pallavi Kumar
Ryan J. Sullivan
6 Parallel and Serial Blockade Strategies in BRAF-Mutant Melanoma
105(32)
Michael A. Davies
7 Targeting the Cell Cycle and p53 in Combination with BRAF-Directed Therapy
137(26)
Dale Han
Keiran SM Smalley
8 Combination BRAF-Directed Therapy and Immunotherapy
163(20)
Zachary A. Cooper
Zain Ahmed
Jennifer A. Wargo
9 Moving Forward: Making BRAF-Targeted Therapy Better
183(20)
Keith T. Flaherty
Index 203
Dr. Ryan J. Sullivan is affiliated with Massachusetts General Hospital and Dana Farber. His research interests are in the development of novel molecular therapeutic agents for Kaposi sarcoma (KS) and malignant melanoma and the translation of promising preclinical findings into early stage clinical trials. He serves as the co-director of the Eugene Michael Egan Melanoma Translational Research Laboratory at Beth Israel Deaconess Medical Center (BIDMC) and is actively investigating promising biomarkers of response and benefit to immunotherapy and molecular targeted therapy for patients with melanoma.