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Advances in Cancer Drug Targets. (Record no. 109364)

MARC details
000 -LEADER
fixed length control field 07938nam a22004813i 4500
001 - CONTROL NUMBER
control field EBC4504170
003 - CONTROL NUMBER IDENTIFIER
control field MiAaPQ
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20240729130433.0
006 - FIXED-LENGTH DATA ELEMENTS--ADDITIONAL MATERIAL CHARACTERISTICS
fixed length control field m o d |
007 - PHYSICAL DESCRIPTION FIXED FIELD--GENERAL INFORMATION
fixed length control field cr cnu||||||||
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 240724s2016 xx o ||||0 eng d
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number 9781681082332
Qualifying information (electronic bk.)
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
Canceled/invalid ISBN 9781681082349
035 ## - SYSTEM CONTROL NUMBER
System control number (MiAaPQ)EBC4504170
035 ## - SYSTEM CONTROL NUMBER
System control number (Au-PeEL)EBL4504170
035 ## - SYSTEM CONTROL NUMBER
System control number (CaPaEBR)ebr11204301
035 ## - SYSTEM CONTROL NUMBER
System control number (OCoLC)948924406
040 ## - CATALOGING SOURCE
Original cataloging agency MiAaPQ
Language of cataloging eng
Description conventions rda
-- pn
Transcribing agency MiAaPQ
Modifying agency MiAaPQ
050 #4 - LIBRARY OF CONGRESS CALL NUMBER
Classification number RC271.C5 -- .A383 2016eb
082 0# - DEWEY DECIMAL CLASSIFICATION NUMBER
Classification number 616.99406099999999
100 1# - MAIN ENTRY--PERSONAL NAME
Personal name Atta-ur-Rahman.
245 10 - TITLE STATEMENT
Title Advances in Cancer Drug Targets.
250 ## - EDITION STATEMENT
Edition statement 1st ed.
264 #1 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Place of production, publication, distribution, manufacture Sharjah :
Name of producer, publisher, distributor, manufacturer Bentham Science Publishers,
Date of production, publication, distribution, manufacture, or copyright notice 2016.
264 #4 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Date of production, publication, distribution, manufacture, or copyright notice ©2016.
300 ## - PHYSICAL DESCRIPTION
Extent 1 online resource (278 pages)
336 ## - CONTENT TYPE
Content type term text
Content type code txt
Source rdacontent
337 ## - MEDIA TYPE
Media type term computer
Media type code c
Source rdamedia
338 ## - CARRIER TYPE
Carrier type term online resource
Carrier type code cr
Source rdacarrier
490 1# - SERIES STATEMENT
Series statement Advances in Cancer Drug Targets ;
Volume/sequential designation v.3
505 0# - FORMATTED CONTENTS NOTE
Formatted contents note Intro -- CONTENTS -- PREFACE -- List of Contributors -- Neutrophil Elastase as a Target in Lung Cancer: the State of the Art -- 1. INTRODUCTION: NEUTROPHIL ELASTASE/Α-1ANTITRYPSIN IMBALANCE AS A LINK BETWEEN CHRONIC OBSTRUCTIVE PULMONARY DISEASE AND LUNG CANCER -- 2. MULTIFACETED FUNCTIONS OF NEUTROPHIL ELASTASE IN LUNG CANCER -- 3. ENDEGNENOUS NEUTROPHIL ELASTASE INHIBITORS -- 3.1. Proteinaceous Inhibitors -- 3.2. Natural Compounds -- 3.2.1. Glycosaminoglycans -- 3.2.2. Phenolics -- 3.2.3. Triterpenoids -- 3.2.4. Fatty Acids and Peptide Derivatives -- 4. DESIGN OF DUAL NEUTROPHIL ELASTASE / MMP INHIBITORS -- DESIGN OF DUAL HNE-MMP INHIBITORS -- CONCLUDING REMARKS -- ADDITIONAL MATERIAL -- 1. Molecular Modeling and Molecular Graphics -- 2. Ligand and Receptor Preparation -- 3. Docking Protocol -- CONFLICT OF INTEREST -- DISCLOSURE -- ACKNOWLEDGEMENTS -- ABBREVIATIONS -- REFERENCES -- Inhibition of Membrane Complement Inhibitor Expression (CD46, CD55, CD59) by siRNA Sensitizes Tumor Cells to Complement Attack -- INTRODUCTION -- MATERIALS AND METHODS -- Cell Culture -- SiRNA Sequences -- SiRNA Transfection -- Flow Cytometry -- Complement-mediated Cytotoxicity Assay (CDC) -- C3-binding Studies -- Real-Time RT-PCR -- Statistical Analysis -- RESULTS -- Design of siRNAs Specific for CD46, CD55 and CD59 -- SiRNA-mediated Downregulation of mCRP Expression -- siRNA-mediated Augmentation of Tumor Cell Complement Lysis and Opsonization -- Time-course of siRNA-induced mCRP Inhibition -- Stable Downregulation of CD59 Using an Hairpin siRNA Expression Vector -- DISCUSSION -- CONFLICT OF INTEREST -- DISCLOSURE -- ACKNOWLEDGEMENT -- ABBREVIATIONS -- REFERENCES -- Points of Therapeutic Intervention along the Wnt Signaling Pathway in Hepatocellular Carcinoma -- INTRODUCTION -- THE WNT SIGNALING PATHWAY -- Overview of the Wnt Signaling -- The Wnt/β-catenin Pathway.
505 8# - FORMATTED CONTENTS NOTE
Formatted contents note Aberrant Activation of the Wnt/β-catenin Pathway in HCC -- TARGETING THE WNT/Β-CATENIN PATHWAY IN HCC -- Targeting the Upstream Components -- Endogenous Inhibitors of the Ligand/Receptor Complex -- Targeting Wnt Ligands and FZD Receptors -- Targeting the Dishevelled Protein -- Cellular Trafficking and Targets -- Targeting the β-catenin Destruction Complex -- Targeting the β-catenin/TCF Transcriptional Complex -- Pitfalls in Targeting the Wnt/β-catenin Pathway -- CONCLUSIONS AND PERSPECTIVES -- CONFLICT OF INTEREST -- DISCLOSURE -- ACKNOWLEDGMENT -- ABBREVIATIONS -- REFERENCES -- Collaboration of Epithelial Mesenchymal Transition and Cancer Stem Cells: Sinister Routes for Chemoresistant Recurrent Ovarian Cancer -- INTRODUCTION -- PATHOLOGY OF OVARIAN CANCER -- TRANSITION FROM EPITHELIAL TO MESENCHYMAL PHENOTYPE AND THE PROGRESSION OF CANCER -- EVIDENCE OF EMT IN OVARIAN CANCER -- STEM CELLS IN NORMAL OVARIES AND OVARIAN CANCER -- SPHERE FORMATION AND THE CANCER STEM CELL PHENOTYPE OF THE OVARY -- ASSOCIATION OF EMT AND CSCS: A MERGER FOR POTENTIAL CHEMORESISTANCE IN OVARIAN CANCER -- Cisplatin Induced EMT Generates Ovarian Cancer Stem-Like Cells: A Study on the OVCA 433 Cell Line as an Experimental Model -- NEW THERAPEUTIC APPROACHES AND CONCLUSION -- CONFLICT OF INTEREST -- DISCLOSURE -- ACKNOWLEDGEMENTS -- ABBREVIATIONS -- REFERENCES -- Oxaliplatin-mediated Inhibition of Survivin Increases Sensitivity of Head and Neck Squamous Cell Carcinoma Cell Lines to Paclitaxel -- INTRODUCTION -- MATERIALS AND METHODS -- Cell Culture -- Plasmid and Antisense Transfection Efficiency -- Drug Treatment -- MTT (methylthiazolyldiphenyl-tetrazolium bromide) Assay -- Western Blot Analysis -- Real-Time PCR -- TUNEL (Terminal Deoxyribonucleotidyl Transferase Mediated dUTP Nick End Labeling) Assay -- Statistical Analysis -- RESULTS.
505 8# - FORMATTED CONTENTS NOTE
Formatted contents note Detection of Survivin Gene Expression -- Effect of Paclitaxel and Oxaliplatin on Cell Growth and Survival -- Survivin Expression Reduces Paclitaxel-mediated Cytotoxicity -- Oxaliplatin Sensitizes Cancer Cells to Paclitaxel by Inhibiting Survivin -- Inhibition of Survivin by a siRNA Method Induces Paclitaxel-mediated Cell Death -- DISCUSSION -- CONFLICT OF INTEREST -- DISCLOSURE -- ACKNOWLEDGEMENTS -- ABBREVIATIONS -- REFERENCES -- Melatonin Inhibits the Growth of DMBA-induced Mammary Tumors by Regulating Estrogen Sulfatase Enzyme -- INTRODUCTION -- MATERIAL AND METHODS -- Animals and Housing Conditions -- Tumor Induction -- Experimental Design -- Surgical Treatments, Tumor Size and Number, Survival Rates and Autopsy Procedures -- Estrone Sulfate and Melatonin Treatments -- Measurement of Steroid Sulfatase Activity -- Measurement of mRNA Expression of Sulfatase -- Statistical Analysis -- RESULTS -- Histopathology of Mammary Tumors -- Evolution of Body Weight -- Tumor Growth -- Survival Probability -- Serum Estradiol Concentration and Uterine Weight -- Sulfatase Activity and Expression -- DISCUSSION -- CONFLICT OF INTEREST -- DISCLOSURE -- ACKNOWLEDGEMENTS -- REFERENCES -- Role of mTOR Signaling in Tumor Cell Motility, Invasion and Metastasis -- INTRODUCTION -- mTOR Strcture and Signaling Complexes -- mTOR Signaling Complexes -- mTORC1 -- mTORC2 -- mTOR Inhibitors -- The Role of mTOR Signaling Pathway in Cell Motility and Invasion -- mTORC1 Signaling in Cell Motility and Invasion -- mTORC2 Signaling in Cell Motility and Invasion -- Rapamycin and Tumor Metastases -- SUMMARY -- CONFLICT OF INTEREST -- DISCLOSURE -- ACKNOWLEDGMENTS -- REFERENCES -- Structure-Activity Studies on Arylamides and Arysulfonamides Ras Inhibitors -- INTRODUCTION -- RESULTS AND DISCUSSION -- Chemistry -- Biochemistry.
505 8# - FORMATTED CONTENTS NOTE
Formatted contents note Interaction between Compound 1 (SCH-53870) and Ras: Preliminary Observations -- Nucleotide Exchange Inhibition Experiments with Compounds 1-17 -- Effect of Compounds 1-4 on Mammalian Cell Growth -- COMPUTATIONAL ANALYSIS -- Docking Calculations -- CONCLUSION -- MATERIALS AND METHODS -- Expression and Isolation of Proteins -- Measurement of GEF-Stimulated Guanine Nucleotide Exchange on p21 h-Ras -- Measurement of Dissociation Rate -- Two-Hybrid System -- Cell Cultures and Growth Conditions -- Docking Calculations -- SUPPLEMENTARY MATERIAL -- CONFLICT OF INTEREST -- DISCLOSURE -- ACKNOWLEDGMENTS -- ABBREVIATIONS -- REFERENCES -- SUBJECT INDEX.
588 ## - SOURCE OF DESCRIPTION NOTE
Source of description note Description based on publisher supplied metadata and other sources.
590 ## - LOCAL NOTE (RLIN)
Local note Electronic reproduction. Ann Arbor, Michigan : ProQuest Ebook Central, 2024. Available via World Wide Web. Access may be limited to ProQuest Ebook Central affiliated libraries.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Cancer--Chemotherapy.
655 #4 - INDEX TERM--GENRE/FORM
Genre/form data or focus term Electronic books.
776 08 - ADDITIONAL PHYSICAL FORM ENTRY
Relationship information Print version:
Main entry heading Atta-ur-Rahman
Title Advances in Cancer Drug Targets
Place, publisher, and date of publication Sharjah : Bentham Science Publishers,c2016
International Standard Book Number 9781681082349
797 2# - LOCAL ADDED ENTRY--CORPORATE NAME (RLIN)
Corporate name or jurisdiction name as entry element ProQuest (Firm)
830 #0 - SERIES ADDED ENTRY--UNIFORM TITLE
Uniform title Advances in Cancer Drug Targets
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://ebookcentral.proquest.com/lib/orpp/detail.action?docID=4504170">https://ebookcentral.proquest.com/lib/orpp/detail.action?docID=4504170</a>
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