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  • 1
    UID:
    almafu_9959328393202883
    Format: 1 online resource
    ISBN: 9781118468685 , 1118468686 , 9781118468661 , 111846866X , 9781118468678 , 1118468678
    Series Statement: Translational oncology
    Note: Targeted and functional imaging / Jian Q. (Michael) Yu, Drew A. Torigian, Abass Alavi -- Combining targeted therapies / Jordi Rodon, Analia Azaro, Davis Torrejon, Razelle Kurzrock -- Toward personalized therapy for cancer / Ashley M. Holder, Funda Meric-Bernstam -- Principles of targeted immunotherapy / Susanne H.C. Baumeister, Glenn Dranoff.
    Additional Edition: Print version: Targeted therapy in translational cancer research. Hoboken, New Jersey : John Wiley & Sons, [2016] ISBN 9781118468579
    Language: English
    Keywords: Electronic books. ; Electronic books. ; Electronic books. ; Electronic books.
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  • 2
    Book
    Book
    Basel : Birkhäuser
    UID:
    kobvindex_ZLB15232448
    Format: VIII, 179 Seiten , Ill. , 235 mm x 165 mm
    Edition: 1. Aufl.
    ISBN: 978-3-7643-8947-5
    Series Statement: Milestones in drug therapy [32]
    Note: Text engl.
    Language: English
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  • 3
    UID:
    gbv_302822437
    Format: XIV, 658 S , Ill., graph. Darst , 28cm
    Edition: 2nd ed
    ISBN: 0721676847
    Language: English
    Keywords: Bluttransfusion
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  • 4
    Online Resource
    Online Resource
    [U.S.A.] :Bentham Science Publishers,
    UID:
    almahu_9948315737502882
    Format: vi, 204 p. : , ill. (some col.), ports.
    Edition: Electronic reproduction. Ann Arbor, MI : ProQuest, 2015. Available via World Wide Web. Access may be limited to ProQuest affiliated libraries.
    Note: section 1. Multiple myeloma -- section 2. Treatment guidelines -- section 3. The bone marrow microenvironment and the pathogenesis of multiple myeloma -- section 4. New treatment strategies.
    Language: English
    Keywords: Electronic books.
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  • 5
    UID:
    almahu_9949419311902882
    Format: VIII, 180 p. , online resource.
    Edition: 1st ed. 2011.
    ISBN: 9783764389482
    Series Statement: Milestones in Drug Therapy,
    Content: Multiple Myeloma (MM) is the second most common type of blood cancer, resulting from an overproduction of cancerous infection-fighting white blood cells, known as plasma cells. Plasma cells are a crucial part of the immune system responsible for the production of antibodies. Bortezomib is a promising anticancer drug targeting the proteasome. This proteasome inhibitor induces cell stress and apoptosis in the cancer cells. While multiple mechanisms are likely to be involved, proteasome inhibition may prevent the degradation of pro-apoptotic factors, permitting activation of programmed cell death in neoplastic cells dependent upon the suppression of proapoptotic pathways. This monograph on bortezomib is a valuable source of information for researchers and clinicians from the fields of oncology and pharmacology, working either in academia or the pharmaceutical industry.
    In: Springer Nature eBook
    Additional Edition: Printed edition: ISBN 9783764389512
    Additional Edition: Printed edition: ISBN 9783034800990
    Additional Edition: Printed edition: ISBN 9783764389475
    Language: English
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  • 6
    UID:
    gbv_1650424841
    Format: Online-Ressource (VIII, 180 p, online resource)
    ISBN: 9783764389482
    Series Statement: Milestones in Drug Therapy
    Content: Multiple Myeloma (MM) is the second most common type of blood cancer, resulting from an overproduction of cancerous infection-fighting white blood cells, known as plasma cells. Plasma cells are a crucial part of the immune system responsible for the production of antibodies. Bortezomib is a promising anticancer drug targeting the proteasome. This proteasome inhibitor induces cell stress and apoptosis in the cancer cells. While multiple mechanisms are likely to be involved, proteasome inhibition may prevent the degradation of pro-apoptotic factors, permitting activation of programmed cell death in neoplastic cells dependent upon the suppression of proapoptotic pathways. This monograph on bortezomib is a valuable source of information for researchers and clinicians from the fields of oncology and pharmacology, working either in academia or the pharmaceutical industry.
    Note: Includes bibliographical references and index , Bortezomib in the Treatment of Multiple Myeloma; Preface; Contents; Bortezomib´s Scientific Origins and Its Tortuous Path to the Clinic; Preclinical Activities of Bortezomib in MM, the Bone Marrow Microenvironment and Pharmacogenomics; Bortezomib and Osteoclasts and Osteoblasts; Bortezomib in the Upfront Treatment of Multiple Myeloma; The Use of Bortezomib in Autologous Transplantation for Multiple Myeloma; Bortezomib in Relapsed and Relapsed/Refractory Multiple Myeloma; Bortezomib-Induced Peripheral Neuropathy in Multiple Myeloma: Principles of Identification and Management , Bortezomib in Mantle Cell LymphomaBortezomib in Waldenstrom´s Macroglobulinemia; Bortezomib in Systemic Light-Chain Amyloidosis; Second-Generation Proteasome Inhibitors; Index
    Additional Edition: ISBN 9783764389475
    Additional Edition: Erscheint auch als Druck-Ausgabe Bortezomib in the treatment of multiple myeloma Basel : Springer, 2011 ISBN 3764389478
    Additional Edition: ISBN 9783764389475
    Language: English
    Subjects: Medicine
    RVK:
    RVK:
    RVK:
    Keywords: Plasmozytom ; Bortezomib ; Bortezomib ; Plasmozytom
    URL: Volltext  (lizenzpflichtig)
    URL: Cover
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  • 7
    UID:
    gbv_1651913633
    Format: Online-Ressource (X, 319 p. 34 illus., 26 illus. in color, digital)
    ISBN: 9781461446668
    Series Statement: SpringerLink
    Content: Despite the advances in conventional, and novel agent and high dose chemotherapy, multiple myeloma remains incurable. In order to overcome resistance to current therapies and improve patient outcome, novel biologically-based treatment approaches are being developed. Current translational research in multiple myeloma focusing on the development of molecularly-based novel targeted single-agent and combination therapies has great promise to achieve high frequency and durable responses in the majority of patients. This volume will focus on biology of multiple myeloma, especially on oncogenomic changes, cell signaling pathways and intermediate molecules that are being investigated for development of novel therapies. The book will present newer developments, providing an emphasis on basic science, as well as its significant clinical impact.
    Note: Description based upon print version of record , Advances in Biology and Therapy of Multiple Myeloma; Preface; Contents; Part I: Myeloma Molecular Pathways and Cell Signaling; Chapter 1: Genomic Strategies Determining Progression from MGUS to Multiple Myeloma; 1.1 Myeloma; 1.2 The Genetics of Plasma Cell Disorders; 1.2.1 Translocation t(11; 14); 1.2.2 Translocation t(4; 14); 1.2.3 Translocation t(14; 16) and Other MAF Translocations; 1.2.4 Deletion of Chromosome 13; 1.2.5 Deletion of 17p13; 1.2.6 Chromosome 1; 1.2.7 RAS Mutations; 1.2.8 Gene Expression Pro fi ling; 1.2.9 High-Throughput Mutation Analysis; 1.2.10 Epigenetic Factors , 1.2.11 Subclonal Heterogeneity1.3 Evaluating Disease Progression; 1.3.1 In Vitro and in Vivo Models of Disease Progression; 1.3.2 Progression of the Disease, Intrinsic Versus Extrinsic; 1.3.3 Clinical Monitoring for Progression; 1.3.4 Public Health Implications; 1.4 Conclusion; References; Chapter 2: Prognostic Implication of Genetic Changes (Cytogenetics, and FISH, Gains and Losses of DNA by SNP Array and aCGH) in Risk Strati fi cation in Myeloma; 2.1 De fi nitions and Technical Aspects; 2.2 Speci fi c Chromosomal Changes; 2.2.1 Aneuploidy; 2.2.2 Chromosome 13 Abnormalities , 2.2.3 Translocations Involving the 14q32 Region2.2.4 Deletions 17p; 2.2.5 Abnormalities of the 1q Region; 2.3 Practical Use of Cytogenetic Data in Routine Practice; 2.4 Genomic Abnormalities in MM; 2.4.1 Minimal Common Regions of Interest with Prognostic Value; 2.4.2 Genes of Interest Residing in MGCL; 2.4.3 Multivariate Analysis of Lesions Independent of Risk Strati fi cation; 2.5 Conclusion; References; Chapter 3: Advances in Multiple Myeloma Gene-Expression Pro fi ling; 3.1 Historical Perspective; 3.2 Microarray Pro fi ling in MM; 3.2.1 MM Cell Procurement Techniques , 3.2.2 Early GEP-Based Studies3.2.3 Early GEP-Based Discoveries of MM Genetic Anomalies; 3.3 GEP-Based MM Classi fi cation; 3.3.1 MS Class; 3.3.2 MF Class; 3.3.3 CD-1 and CD-2 Classes; 3.3.4 HY Class; 3.3.5 LB Class; 3.3.6 PR Class; 3.3.7 Classi fi cation Outliers; 3.4 MM-Speci fi c Genetic Features and GEP; 3.4.1 GEP and Hyperdiploid Disease; 3.4.2 GEP and Chromosome 13 Deletion; 3.4.3 GEP and Gains of Chromosome 1q; 3.4.4 GEP and Deletion of 17p13/TP53; 3.5 GEP-Based MM Risk Strati fi cation; 3.5.1 GEP-De fi ned High-Risk MM; 3.5.2 Progression of Low-Risk to High-Risk at Relapse , 3.5.3 GEP and the Centrosome Index3.5.4 GEP and CD200; 3.6 GEP in MM Therapeutic Decision-Making; 3.6.1 GEP and Cancer-Testis Antigen Expression in MM; 3.6.2 GEP and IGF Signaling; 3.6.3 Pharmacogenomic Studies of Short-Term In Vivo Exposure; 3.7 Conclusions; References; Chapter 4: Growth Factors in Multiple Myeloma; 4.1 Myeloma Cell Growth Factors; 4.1.1 MMC Autocrine Growth Factors; 4.1.2 Bone Marrow Stromal Cell-Produced Growth Factors; 4.1.3 Osteoclast-Produced Growth Factors; 4.1.4 BM Endothelial Cell-Produced Growth Factors; 4.1.5 BM Immune Cell-Produced Growth Factors , 4.1.6 Adipocyte-Produced Growth Factors , Genomic strategies determining progressions from MGUS to Multiple Myeloma -- Prognostic implication of Genetic changes (Cytogenetics, and FISH, gains and losses of DNA by SNP array and aCGH) in risk stratification in myeloma -- Advances in MM gene expression profiling -- Growth factors in MM -- Role of Wnt signaling pathways in multiple myeloma pathogenesis -- mTOR pathway in multiple myeloma -- Jak/STAT signaling in the pathogenesis and treatment of multiple myeloma -- Role of extracellular matrix in myeloma biology -- Osteoclasts: Potential target for blocking microenvironmental support of myeloma -- Targeting the BAFF/APRIL cytokine network in multiple myeloma -- Role of Osteoblast in myeloma pathology -- Migration and homing in Multiple Myeloma -- Genes and proteins of myeloma endothelial cells to search specific targets of the tumor vasculature -- Epigenetic regulation of myeloma within its bone marrow microenvironment -- Targeting mulitple myeloma tumor angiogenesis: focus on VEGF -- Novel in vivo model in myeloma -- Index.
    Additional Edition: ISBN 9781461446651
    Additional Edition: Buchausg. u.d.T. ISBN 978-1-461-44665-1
    Language: English
    URL: Volltext  (lizenzpflichtig)
    URL: Cover
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  • 8
    UID:
    gbv_1651955530
    Format: Online-Ressource (X, 287 p. 7 illus., 5 illus. in color, digital)
    ISBN: 9781461452607
    Series Statement: SpringerLink
    Content: Despite the advances in conventional, and novel agent and high dose chemotherapy, multiple myeloma remains incurable. In order to overcome resistance to current therapies and improve patient outcome, novel biologically-based treatment approaches are being developed. Current translational research in multiple myeloma focusing on the development of molecularly-based novel targeted single-agent and combination therapies has great promise to achieve high frequency and durable responses in the majority of patients. This volume will focus on biology of multiple myeloma, especially on oncogenomic changes, cell signaling pathways and intermediate molecules that are being investigated for development of novel therapies. The book will present newer developments, providing an emphasis on basic science, as well as its significant clinical impact.
    Note: Description based upon print version of record , T cell responses in myeloma -- Novel antigenic targets for immunotherapy in myeloma -- Antibody-based therapies in Multiple Myeloma -- Defining multiple myeloma as a target for DNA gene fusion vaccines -- Harnessing allogeneic immunity for anti-myeloma response -- Dendritic cell and peptide-based vaccination in myeloma -- New Proteasome inhibitors -- Newer Imids -- New agents in myeloma -- Early Combination Studies in MM -- The effect of novel antimyeloma agents on bone metabolism -- Index.
    Additional Edition: ISBN 9781461452591
    Additional Edition: Buchausg. u.d.T. ISBN 978-1-461-45259-1
    Language: English
    URL: Volltext  (lizenzpflichtig)
    URL: Cover
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  • 9
    Online Resource
    Online Resource
    [U.S.A.] :Bentham Science Publishers,
    UID:
    almafu_9959237387602883
    Format: 1 online resource (217 p.)
    Edition: 1st ed.
    ISBN: 1-60805-297-4
    Content: Multiple Myeloma (MM), the second most common blood cancer in adults, is a clonal plasma cell malignancy within the bone marrow characterized by osteolytic bone lesions, renal disease, and immunodeficiency. It is now well established that MM cell- induced disruption of the bone marrow homeostasis between the highly organized cellular and extracellular compartments supports MM cell proliferation, survival, migration, and drug resistance via activation of various signaling pathways. Based on this knowledge, the prototypic drugs thalidomide, bortezomib, and lenalidomide, which target both MM cell
    Note: Description based upon print version of record. , section 1. Multiple myeloma -- section 2. Treatment guidelines -- section 3. The bone marrow microenvironment and the pathogenesis of multiple myeloma -- section 4. New treatment strategies. , English
    Additional Edition: ISBN 1-60805-609-0
    Language: English
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