Lung cancer : methods and protocols 🔍
Pedro G. Santiago-Cardona (eds.)
Springer US : Imprint: Humana, Methods in molecular biology (Clifton, N.J. Online), 1st ed. 2021, New York, NY, 2021
英语 [en] · PDF · 7.6MB · 2021 · 📘 非小说类图书 · 🚀/lgli/lgrs/nexusstc/scihub/upload/zlib · Save
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Methods in Molecular Biology
Erscheinungsdatum: 09.03.2021
Erscheinungsdatum: 09.03.2021
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lgli/P:\springer_dnd140621\springer/10.1007%2F978-1-0716-1278-1.pdf
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nexusstc/Lung Cancer: Methods and Protocols/723afbba596f384a9221f9738841336c.pdf
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lgrsnf/Lung_Cancer_by_Pedro_G._Santiago-Cardona.pdf
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scihub/10.1007/978-1-0716-1278-1.pdf
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Humana Press
备用版本
Methods in molecular biology, Boston, 2021
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United States, United States of America
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{"container_title":"Methods in Molecular Biology","isbns":["1071612778","1071612786","9781071612774","9781071612781"],"issns":["1064-3745","1940-6029"],"publisher":"Springer US"}
备用描述
Preface
Contents
Contributors
Chapter 1: Automated TTF-1 Immunohistochemistry Assay for the Differentiation of Lung Adenocarcinoma Versus Lung Squamous Cell...
1 Introduction
2 Materials
2.1 Ready to Use Reagents (see Note 1)
2.2 Immunohistochemistry and Histology Reagents
2.3 Additional Equipment and Materials
3 Methods
3.1 Tissue Fixation and Processing
3.2 Tissue Sectioning
3.3 Immunohistochemistry Staining in the Dako Omnis IHC Staining System
3.4 Counterstaining
3.5 Cover Slipping
3.6 Staining Evaluation and Interpretation
4 Notes
References
Chapter 2: Immunohistochemical Detection of p40 Expression in Lung Cancer Clinical Samples
1 Introduction
2 Materials
2.1 IHC Buffer Solutions and Histology Reagents
2.2 Antibodies and Detection Kits
2.3 Laboratory Equipment
3 Methods
4 Notes
References
Chapter 3: Automated Immunohistochemistry Assay for the Detection of Napsin-A in Formalin-Fixed Paraffin-Embedded Tissues from...
1 Introduction
2 Materials
2.1 Standard Histology Reagents
2.2 Immunohistochemistry Kits, Antibodies and Reagents
2.3 Laboratory Equipment and Consumables
3 Methods
3.1 Reagent Preparation
3.2 Tissue Fixation and Processing
3.3 Tissue Sectioning
3.4 Immunohistochemistry Staining in the Dako Omnis IHC Staining System
3.5 Cover Slipping
3.6 Staining Evaluation and Interpretation
4 Notes
References
Chapter 4: Detection of Programmed Cell Death Ligand 1 Expression in Lung Cancer Clinical Samples by an Automated Immunohistoc...
1 Introduction
2 Materials
2.1 IHC Reagents and Antibody Clones
2.2 IHC Equipment
2.3 Standard Reagents and Additional Equipment
3 Methods
3.1 Automated PD-L1 Immunohistochemistry Staining
3.2 Image Acquisition, Digital Analysis and Staining Analysis
4 Notes
References
Chapter 5: Western Blot as a Support Technique for Immunohistochemistry to Detect Programmed Cell Death Ligand 1 Expression
1 Introduction
2 Materials
2.1 Gel Electrophoresis Separation
2.2 Protein Transfer
2.3 Membrane Blocking, Immunolabeling, Washing and Development
2.4 Cell Lines and Tissues
2.5 Additional Materials
3 Methods
3.1 Sample Preparation, Electrophoresis, and Transfer
3.2 Immunolabeling and Signal Development
4 Notes
References
Chapter 6: Creation of Formalin-Fixed, Paraffin-Embedded 3D Lung Cancer Cellular Spheroids for the Optimization of Immunohisto...
1 Introduction
2 Materials
2.1 Cell Lines and Cell Culture Reagents
2.2 Histology Reagents and Supplies
2.3 Immunohistochemistry Reagents
2.4 General Laboratory Equipment
3 Methods
3.1 Spheroid Preparation from Cell Cultures
3.2 Preparation of Spheroid Paraffin Blocks
3.3 Microtome Sectioning of Spheroid Paraffin Blocks
3.4 Hematoxylin and Eosin (H&E) Staining
3.5 Immunohistochemistry (IHC) of Spheroid Sections
4 Notes
References
Chapter 7: Immunoblot Validation of Phospho-Specific Antibodies Using Lung Cancer Cell Lines
1 Introduction
2 Materials
2.1 Cell Lysis and Protein Extraction and Quantification
2.2 Alkaline Bovine Intestinal Phosphatase (BIP) Treatment of Protein Lysates
2.3 SDS Polyacrylamide Gel Electrophoresis
2.4 Transfer
2.5 Immunoblotting Reagents
2.6 Additional Laboratory Equipment and Plasticware
3 Methods
3.1 Cell Lysis and Preparation of Protein Extracts
3.2 Protein Lysate Dephosphorylation with Alkaline Bovine Intestinal Phosphatase (BIP)
3.3 SDS Polyacrylamide Gel Electrophoresis and Transfer
3.4 Transfer of Proteins to Nitrocellulose Membranes
3.5 Immunoblotting, Image Development, and Capture
3.6 Interpretation of Results
4 Notes
References
Chapter 8: Detection of Non-Small Lung Cell Carcinoma-Associated Genetic Alterations Using a NanoString Gene Expression Platfo...
1 Introduction
2 Materials
2.1 Tumor Cell Content Assessment
2.2 DNA/RNA Extraction
2.3 NanoString Fusion Gene Detection
2.4 NanoString Gene Expression
2.5 General Laboratory Equipment, Supplies and Reagents
3 Methods
3.1 RNA/DNA Extraction
3.2 Fusion Gene Detection Using the NanoString Technology
3.2.1 Hybridization Using the nCounter Elements Chemistry (Combined Gene Expression and Fusion Gene Detection)
3.2.2 Hybridization Using the nCounter XT Chemistry (Gene Expression Only)
3.2.3 Operating the NanoString SPRINT Instrument
3.2.4 NanoString Data Processing
3.3 Final Report of NanoString Fusion Gene Detection and Gene Expression Profiling
4 Notes
References
Chapter 9: A PCR-Based Approach for Driver Mutation Analysis of EGFR, KRAS, and BRAF Genes in Lung Cancer Tissue Sections
1 Introduction
1.1 Driver Genes in Lung Cancer: Focus on Personalized Medicine
1.2 The Polymerase Chain Reaction Technique: Basis and Principles
1.3 PCR-Based Approach for Mutational Analysis of EGFR, KRAS, and BRAF Genes
2 Materials
2.1 Histology Reagents and Materials
2.2 Reagents and Kits for DNA Extraction, PCR, and Sequencing
2.3 General Laboratory Equipment
2.4 General Use Laboratory Consumables
3 Methods
3.1 DNA Isolation from Lung Tumor Tissue Sections
3.1.1 Deparaffinization of Tissues
3.1.2 Tissue Digestion and DNA Extraction from Tumor Tissue Sections
3.2 PCR Amplification of EGFR, KRAS, and BRAF Hotspot Regions
3.3 Direct Sanger Sequencing
3.3.1 Purification of the PCR Product for Sequencing
3.3.2 Assembly of the Sequencing Reaction
3.3.3 Sequencing Reaction Steps
3.3.4 Purification of Sequencing Yield
3.3.5 Genetic Analysis
4 Notes
References
Chapter 10: 6-Color Crystal Digital PCRTM for the High-Plex Detection of EGFR Mutations in Non-Small Cell Lung Cancer
1 Introduction
1.1 Genetic Mutations Commonly Associated with Non-small Cell Lung Cancer
1.2 The Naica system Enables Robust Tumor-Derived DNA Analysis
1.3 The Naica system 6-Color Digital PCR EGFR Assay
2 Materials
2.1 General Plasticware and Laboratory Equipment
2.2 PCR Equipment and Software
2.3 DNA Extraction and Quantification
2.4 PCR Reagents and Solutions
3 Methods
3.1 DNA Template Preparation and PCR Setup
3.2 Setting up the Fluorescence Spillover Compensation Matrix Using Control Samples
3.3 Data Acquisition and Analysis of Test Samples
3.4 Limit of Blank (LOB) Determination and Data Interpretation
4 Notes
References
Chapter 11: Detection of MET Exon 14 Skipping Alterations in Lung Cancer Clinical Samples Using a PCR-Based Approach
1 Introduction
2 Materials
2.1 Isolation of Total RNA from Fresh Tissue
2.2 Isolation of Total RNA from Formalin Fixed Paraffin Embedded (FFPE) Sections
2.3 PCR Detection of METex14 Skipped Samples
3 Methods
3.1 RNA Isolation from Fresh Tissues
3.2 RNA Isolation from FFPE Tissues
3.3 Detection of METex14 Skipped Samples Using PCR
3.4 Agarose Gel Electrophoresis
4 Notes
References
Chapter 12: Immunocytochemical Detection of ALK and ROS1 Rearrangements in Lung Cancer Cytological Samples
1 Introduction
2 Materials
2.1 Laboratory Equipment
2.2 General Reagents and Solutions and Immunohistochemistry Reagents
3 Methods
3.1 Slide Preparation
3.2 Immunocytochemistry
3.3 Data Analysis
4 Notes
References
Chapter 13: A Method for the Establishment of Human Lung Adenocarcinoma Patient-Derived Xenografts in Mice
1 Introduction
2 Materials
2.1 Materials, Laboratory Equipment, and Solutions for Tumor Implantation
2.2 Materials for Tumor Freeze Down
2.3 Materials for Peripheral Blood Mononuclear Cell (PBMC) Engraftment
2.4 Materials for Generating and Freezing Tumor Cell Suspension
3 Methods
3.1 Subcutaneous Implantation of Tumor Pieces
3.2 Freezing of Tumor Pieces for PDXs
3.3 Engrafting PBMCs into Immunodeficient Mice
3.4 Subcutaneous Implantation of Tumor Cells into Immunodeficient Mice
3.5 Freezing Tumor Cells for PDXs
4 Notes
References
Chapter 14: A Method for the Establishment and Characterization of Mouse Lung Adenocarcinoma Cell Lines that Mimic Traits of H...
1 Introduction
2 Materials
2.1 Solutions and Reagents
2.2 Mice and Surgical Procedure Equipment
2.3 Laboratory Equipment
2.4 Plasticware and Other Consumables
3 Methods
3.1 Injection of Carcinogen to Mice
3.2 Isolation of Lung Tumors
3.3 Histology and Lung Adenocarcinoma Diagnosis
3.3.1 Tissue Preparation for Histology
3.3.2 H&E Staining
3.3.3 Periodic Acid-Schiff Staining with (α-Amylase) Diastase (PAS-D)
3.4 Immunohistochemical Localization of Lung Adenocarcinoma Markers
3.5 Derivation of Mouse Lung Adenocarcinoma Cell Lines
3.6 In Vitro Validation of Proliferative Capacity by MTT Assay
3.7 In Vitro Validation of Stemness by Tumorsphere Formation Assay
3.8 In Vivo Validation of Malignancy and Spontaneous Metastatic Potential by Flank Assay
4 Notes
References
Chapter 15: Whole Transcriptome Sequencing Analysis of Cancer Stem/Progenitor Cells Obtained from Mouse Lung Adenocarcinomas
1 Introduction
2 Materials
2.1 Cell Culture
2.2 RNA Extraction
2.3 RNA-Seq Workflow and Analysis, Kits and Software
2.4 Reverse Transcription of RNA to cDNA
2.5 General Laboratory Equipment, Supplies, and Solutions
3 Methods
3.1 Culturing Cells for Sphere-Formation Assay
3.2 Preparation of Cell Suspension in Matrigel Mixture at a Defined Plating Density
3.3 Plating the Cell Suspension in Matrigel for Sphere-Formation Assay
3.4 Calculation of Sphere-Formation Efficiency
3.5 Sphere Propagation
3.6 RNA Isolation from Lung Cancer Spheres
3.7 Whole Transcriptome Sequencing
3.7.1 Experimental Workflow
3.7.2 Analysis Workflow
3.8 Interrogation of Select Differentially Expressed Genes by Quantitative Real Time PCR (qRT-PCR)
3.8.1 Reverse Transcription of RNA to cDNA
4 Notes
References
Chapter 16: In Vivo Imaging of Orthotopic Lung Cancer Models in Mice
1 Introduction
2 Materials
2.1 Cell Lines and Culture Reagents
2.2 Plasticware for Cell Cultures
2.3 Mice and Related Materials and Solutions
2.4 Equipment
2.5 Software
3 Methods
3.1 Cell Culture
3.2 Preparation of Cellular Suspension for Injection
3.3 Intravenous Injection of TC1-Luc Cells
3.4 Intercostal Injection of LLC-Luc Cells
3.5 Bioluminescent Imaging and Data Analysis
3.6 Preparation of Reagents and Treatments of Tumor Bearing Mice
4 Notes
References
Chapter 17: An Annexin V-FITC-Propidium Iodide-Based Method for Detecting Apoptosis in a Non-Small Cell Lung Cancer Cell Line
1 Introduction
2 Materials
2.1 Reagents and Solutions
2.2 Cell Culture Reagents and Equipment
2.3 Other Labware and Equipment
3 Methods
3.1 Cell Preparation and Drug Treatment
3.2 Cell Staining
3.3 Flow Cytometer Instrument Setup
3.4 Cell Analysis
4 Notes
References
Chapter 18: Detection of DNA Adduct Formation in Rat Lungs by a Micro-HPLC/MS/MS Approach
1 Introduction
2 Materials
2.1 Synthesis, Purification, and Characterization of 1,N2-propanodGuo, [15N5]-1,N2-propanodGuo and [13C2,15N5]-1,N2-propanodGuo
2.2 DNA Extraction and Enzymatic Hydrolysis
2.3 Quantification of 2′-Deoxyguanosine
2.4 Enrichment and Purification of the 1,N2-propanodGuo Adducts
2.5 Analysis by Micro-LC-ESI/MS/MS of 1,N2-propanodGuo in Rats
3 Methods
3.1 Synthesis of 1,N2-propanodGuo, [15N5]-1,N2-propanodGuo and [13C4,15N5]-1,N2-propanodGuo Standards
3.2 DNA Extraction and Enzymatic Hydrolysis
3.3 Quantification of 2′-Deoxyguanosine
3.4 Enrichment and Purification of the 1,N2-propanodGuo Adducts
3.5 Analysis by Micro-LC-ESI/MS/MS of 1,N2-propanodGuo in Rat Lungs
4 Notes
References
Chapter 19: A Method for Liposome Co-encapsulation of Phenethyl Isothiocyanate and Cisplatin and Determining Its Toxicity Agai...
1 Introduction
2 Materials
2.1 Liposome Preparation
2.2 1,2-Benzenedithiol (BDT) Assay
2.3 Release
2.4 Cell Lines, Cell Culture Media, and Cytotoxicity Assay Reagents
2.5 Additional Laboratory Equipment and Reagents
3 Methods
3.1 Preparation and Characterization of Liposomes
3.2 Determination of PEITC Loading in Liposomal-PEITC and Liposomal-PEITC-CDDP Using 1,2-Benzenedithiol (BDT) Assay
3.3 Determination of CDDP Loading in Liposomal-CDDP and Liposomal-PEITC-CDDP by Inductively Coupled Plasma-Mass Spectrometry (...
3.4 In Vitro Drug Release Studies
3.5 Cytotoxicity Studies
4 Notes
References
Index
Contents
Contributors
Chapter 1: Automated TTF-1 Immunohistochemistry Assay for the Differentiation of Lung Adenocarcinoma Versus Lung Squamous Cell...
1 Introduction
2 Materials
2.1 Ready to Use Reagents (see Note 1)
2.2 Immunohistochemistry and Histology Reagents
2.3 Additional Equipment and Materials
3 Methods
3.1 Tissue Fixation and Processing
3.2 Tissue Sectioning
3.3 Immunohistochemistry Staining in the Dako Omnis IHC Staining System
3.4 Counterstaining
3.5 Cover Slipping
3.6 Staining Evaluation and Interpretation
4 Notes
References
Chapter 2: Immunohistochemical Detection of p40 Expression in Lung Cancer Clinical Samples
1 Introduction
2 Materials
2.1 IHC Buffer Solutions and Histology Reagents
2.2 Antibodies and Detection Kits
2.3 Laboratory Equipment
3 Methods
4 Notes
References
Chapter 3: Automated Immunohistochemistry Assay for the Detection of Napsin-A in Formalin-Fixed Paraffin-Embedded Tissues from...
1 Introduction
2 Materials
2.1 Standard Histology Reagents
2.2 Immunohistochemistry Kits, Antibodies and Reagents
2.3 Laboratory Equipment and Consumables
3 Methods
3.1 Reagent Preparation
3.2 Tissue Fixation and Processing
3.3 Tissue Sectioning
3.4 Immunohistochemistry Staining in the Dako Omnis IHC Staining System
3.5 Cover Slipping
3.6 Staining Evaluation and Interpretation
4 Notes
References
Chapter 4: Detection of Programmed Cell Death Ligand 1 Expression in Lung Cancer Clinical Samples by an Automated Immunohistoc...
1 Introduction
2 Materials
2.1 IHC Reagents and Antibody Clones
2.2 IHC Equipment
2.3 Standard Reagents and Additional Equipment
3 Methods
3.1 Automated PD-L1 Immunohistochemistry Staining
3.2 Image Acquisition, Digital Analysis and Staining Analysis
4 Notes
References
Chapter 5: Western Blot as a Support Technique for Immunohistochemistry to Detect Programmed Cell Death Ligand 1 Expression
1 Introduction
2 Materials
2.1 Gel Electrophoresis Separation
2.2 Protein Transfer
2.3 Membrane Blocking, Immunolabeling, Washing and Development
2.4 Cell Lines and Tissues
2.5 Additional Materials
3 Methods
3.1 Sample Preparation, Electrophoresis, and Transfer
3.2 Immunolabeling and Signal Development
4 Notes
References
Chapter 6: Creation of Formalin-Fixed, Paraffin-Embedded 3D Lung Cancer Cellular Spheroids for the Optimization of Immunohisto...
1 Introduction
2 Materials
2.1 Cell Lines and Cell Culture Reagents
2.2 Histology Reagents and Supplies
2.3 Immunohistochemistry Reagents
2.4 General Laboratory Equipment
3 Methods
3.1 Spheroid Preparation from Cell Cultures
3.2 Preparation of Spheroid Paraffin Blocks
3.3 Microtome Sectioning of Spheroid Paraffin Blocks
3.4 Hematoxylin and Eosin (H&E) Staining
3.5 Immunohistochemistry (IHC) of Spheroid Sections
4 Notes
References
Chapter 7: Immunoblot Validation of Phospho-Specific Antibodies Using Lung Cancer Cell Lines
1 Introduction
2 Materials
2.1 Cell Lysis and Protein Extraction and Quantification
2.2 Alkaline Bovine Intestinal Phosphatase (BIP) Treatment of Protein Lysates
2.3 SDS Polyacrylamide Gel Electrophoresis
2.4 Transfer
2.5 Immunoblotting Reagents
2.6 Additional Laboratory Equipment and Plasticware
3 Methods
3.1 Cell Lysis and Preparation of Protein Extracts
3.2 Protein Lysate Dephosphorylation with Alkaline Bovine Intestinal Phosphatase (BIP)
3.3 SDS Polyacrylamide Gel Electrophoresis and Transfer
3.4 Transfer of Proteins to Nitrocellulose Membranes
3.5 Immunoblotting, Image Development, and Capture
3.6 Interpretation of Results
4 Notes
References
Chapter 8: Detection of Non-Small Lung Cell Carcinoma-Associated Genetic Alterations Using a NanoString Gene Expression Platfo...
1 Introduction
2 Materials
2.1 Tumor Cell Content Assessment
2.2 DNA/RNA Extraction
2.3 NanoString Fusion Gene Detection
2.4 NanoString Gene Expression
2.5 General Laboratory Equipment, Supplies and Reagents
3 Methods
3.1 RNA/DNA Extraction
3.2 Fusion Gene Detection Using the NanoString Technology
3.2.1 Hybridization Using the nCounter Elements Chemistry (Combined Gene Expression and Fusion Gene Detection)
3.2.2 Hybridization Using the nCounter XT Chemistry (Gene Expression Only)
3.2.3 Operating the NanoString SPRINT Instrument
3.2.4 NanoString Data Processing
3.3 Final Report of NanoString Fusion Gene Detection and Gene Expression Profiling
4 Notes
References
Chapter 9: A PCR-Based Approach for Driver Mutation Analysis of EGFR, KRAS, and BRAF Genes in Lung Cancer Tissue Sections
1 Introduction
1.1 Driver Genes in Lung Cancer: Focus on Personalized Medicine
1.2 The Polymerase Chain Reaction Technique: Basis and Principles
1.3 PCR-Based Approach for Mutational Analysis of EGFR, KRAS, and BRAF Genes
2 Materials
2.1 Histology Reagents and Materials
2.2 Reagents and Kits for DNA Extraction, PCR, and Sequencing
2.3 General Laboratory Equipment
2.4 General Use Laboratory Consumables
3 Methods
3.1 DNA Isolation from Lung Tumor Tissue Sections
3.1.1 Deparaffinization of Tissues
3.1.2 Tissue Digestion and DNA Extraction from Tumor Tissue Sections
3.2 PCR Amplification of EGFR, KRAS, and BRAF Hotspot Regions
3.3 Direct Sanger Sequencing
3.3.1 Purification of the PCR Product for Sequencing
3.3.2 Assembly of the Sequencing Reaction
3.3.3 Sequencing Reaction Steps
3.3.4 Purification of Sequencing Yield
3.3.5 Genetic Analysis
4 Notes
References
Chapter 10: 6-Color Crystal Digital PCRTM for the High-Plex Detection of EGFR Mutations in Non-Small Cell Lung Cancer
1 Introduction
1.1 Genetic Mutations Commonly Associated with Non-small Cell Lung Cancer
1.2 The Naica system Enables Robust Tumor-Derived DNA Analysis
1.3 The Naica system 6-Color Digital PCR EGFR Assay
2 Materials
2.1 General Plasticware and Laboratory Equipment
2.2 PCR Equipment and Software
2.3 DNA Extraction and Quantification
2.4 PCR Reagents and Solutions
3 Methods
3.1 DNA Template Preparation and PCR Setup
3.2 Setting up the Fluorescence Spillover Compensation Matrix Using Control Samples
3.3 Data Acquisition and Analysis of Test Samples
3.4 Limit of Blank (LOB) Determination and Data Interpretation
4 Notes
References
Chapter 11: Detection of MET Exon 14 Skipping Alterations in Lung Cancer Clinical Samples Using a PCR-Based Approach
1 Introduction
2 Materials
2.1 Isolation of Total RNA from Fresh Tissue
2.2 Isolation of Total RNA from Formalin Fixed Paraffin Embedded (FFPE) Sections
2.3 PCR Detection of METex14 Skipped Samples
3 Methods
3.1 RNA Isolation from Fresh Tissues
3.2 RNA Isolation from FFPE Tissues
3.3 Detection of METex14 Skipped Samples Using PCR
3.4 Agarose Gel Electrophoresis
4 Notes
References
Chapter 12: Immunocytochemical Detection of ALK and ROS1 Rearrangements in Lung Cancer Cytological Samples
1 Introduction
2 Materials
2.1 Laboratory Equipment
2.2 General Reagents and Solutions and Immunohistochemistry Reagents
3 Methods
3.1 Slide Preparation
3.2 Immunocytochemistry
3.3 Data Analysis
4 Notes
References
Chapter 13: A Method for the Establishment of Human Lung Adenocarcinoma Patient-Derived Xenografts in Mice
1 Introduction
2 Materials
2.1 Materials, Laboratory Equipment, and Solutions for Tumor Implantation
2.2 Materials for Tumor Freeze Down
2.3 Materials for Peripheral Blood Mononuclear Cell (PBMC) Engraftment
2.4 Materials for Generating and Freezing Tumor Cell Suspension
3 Methods
3.1 Subcutaneous Implantation of Tumor Pieces
3.2 Freezing of Tumor Pieces for PDXs
3.3 Engrafting PBMCs into Immunodeficient Mice
3.4 Subcutaneous Implantation of Tumor Cells into Immunodeficient Mice
3.5 Freezing Tumor Cells for PDXs
4 Notes
References
Chapter 14: A Method for the Establishment and Characterization of Mouse Lung Adenocarcinoma Cell Lines that Mimic Traits of H...
1 Introduction
2 Materials
2.1 Solutions and Reagents
2.2 Mice and Surgical Procedure Equipment
2.3 Laboratory Equipment
2.4 Plasticware and Other Consumables
3 Methods
3.1 Injection of Carcinogen to Mice
3.2 Isolation of Lung Tumors
3.3 Histology and Lung Adenocarcinoma Diagnosis
3.3.1 Tissue Preparation for Histology
3.3.2 H&E Staining
3.3.3 Periodic Acid-Schiff Staining with (α-Amylase) Diastase (PAS-D)
3.4 Immunohistochemical Localization of Lung Adenocarcinoma Markers
3.5 Derivation of Mouse Lung Adenocarcinoma Cell Lines
3.6 In Vitro Validation of Proliferative Capacity by MTT Assay
3.7 In Vitro Validation of Stemness by Tumorsphere Formation Assay
3.8 In Vivo Validation of Malignancy and Spontaneous Metastatic Potential by Flank Assay
4 Notes
References
Chapter 15: Whole Transcriptome Sequencing Analysis of Cancer Stem/Progenitor Cells Obtained from Mouse Lung Adenocarcinomas
1 Introduction
2 Materials
2.1 Cell Culture
2.2 RNA Extraction
2.3 RNA-Seq Workflow and Analysis, Kits and Software
2.4 Reverse Transcription of RNA to cDNA
2.5 General Laboratory Equipment, Supplies, and Solutions
3 Methods
3.1 Culturing Cells for Sphere-Formation Assay
3.2 Preparation of Cell Suspension in Matrigel Mixture at a Defined Plating Density
3.3 Plating the Cell Suspension in Matrigel for Sphere-Formation Assay
3.4 Calculation of Sphere-Formation Efficiency
3.5 Sphere Propagation
3.6 RNA Isolation from Lung Cancer Spheres
3.7 Whole Transcriptome Sequencing
3.7.1 Experimental Workflow
3.7.2 Analysis Workflow
3.8 Interrogation of Select Differentially Expressed Genes by Quantitative Real Time PCR (qRT-PCR)
3.8.1 Reverse Transcription of RNA to cDNA
4 Notes
References
Chapter 16: In Vivo Imaging of Orthotopic Lung Cancer Models in Mice
1 Introduction
2 Materials
2.1 Cell Lines and Culture Reagents
2.2 Plasticware for Cell Cultures
2.3 Mice and Related Materials and Solutions
2.4 Equipment
2.5 Software
3 Methods
3.1 Cell Culture
3.2 Preparation of Cellular Suspension for Injection
3.3 Intravenous Injection of TC1-Luc Cells
3.4 Intercostal Injection of LLC-Luc Cells
3.5 Bioluminescent Imaging and Data Analysis
3.6 Preparation of Reagents and Treatments of Tumor Bearing Mice
4 Notes
References
Chapter 17: An Annexin V-FITC-Propidium Iodide-Based Method for Detecting Apoptosis in a Non-Small Cell Lung Cancer Cell Line
1 Introduction
2 Materials
2.1 Reagents and Solutions
2.2 Cell Culture Reagents and Equipment
2.3 Other Labware and Equipment
3 Methods
3.1 Cell Preparation and Drug Treatment
3.2 Cell Staining
3.3 Flow Cytometer Instrument Setup
3.4 Cell Analysis
4 Notes
References
Chapter 18: Detection of DNA Adduct Formation in Rat Lungs by a Micro-HPLC/MS/MS Approach
1 Introduction
2 Materials
2.1 Synthesis, Purification, and Characterization of 1,N2-propanodGuo, [15N5]-1,N2-propanodGuo and [13C2,15N5]-1,N2-propanodGuo
2.2 DNA Extraction and Enzymatic Hydrolysis
2.3 Quantification of 2′-Deoxyguanosine
2.4 Enrichment and Purification of the 1,N2-propanodGuo Adducts
2.5 Analysis by Micro-LC-ESI/MS/MS of 1,N2-propanodGuo in Rats
3 Methods
3.1 Synthesis of 1,N2-propanodGuo, [15N5]-1,N2-propanodGuo and [13C4,15N5]-1,N2-propanodGuo Standards
3.2 DNA Extraction and Enzymatic Hydrolysis
3.3 Quantification of 2′-Deoxyguanosine
3.4 Enrichment and Purification of the 1,N2-propanodGuo Adducts
3.5 Analysis by Micro-LC-ESI/MS/MS of 1,N2-propanodGuo in Rat Lungs
4 Notes
References
Chapter 19: A Method for Liposome Co-encapsulation of Phenethyl Isothiocyanate and Cisplatin and Determining Its Toxicity Agai...
1 Introduction
2 Materials
2.1 Liposome Preparation
2.2 1,2-Benzenedithiol (BDT) Assay
2.3 Release
2.4 Cell Lines, Cell Culture Media, and Cytotoxicity Assay Reagents
2.5 Additional Laboratory Equipment and Reagents
3 Methods
3.1 Preparation and Characterization of Liposomes
3.2 Determination of PEITC Loading in Liposomal-PEITC and Liposomal-PEITC-CDDP Using 1,2-Benzenedithiol (BDT) Assay
3.3 Determination of CDDP Loading in Liposomal-CDDP and Liposomal-PEITC-CDDP by Inductively Coupled Plasma-Mass Spectrometry (...
3.4 In Vitro Drug Release Studies
3.5 Cytotoxicity Studies
4 Notes
References
Index
备用描述
"This detailed book serves as a laboratory manual containing vital protocols and in-depth discussion involving commonly used experimental approaches for the characterization of several aspects of lung tumor biology. Beginning with an extensive section on biomarker detection, the volume continues with chapters on the genetic and molecular characterization of lung cancer biological samples as well as protocols for the generation of research tools and pre-clinical lung cancer models. Written for the highly successful Methods in Molecular Biology series, chapters include introductions to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible protocols, and tips on troubleshooting and avoiding known pitfalls. Authoritative and practical, Lung Cancer: Methods and Protocols provides a global perspective of research efforts related to lung cancer, while allowing researchers to experimentally probe the different aspects of lung cancer research, including the experimentally relevant tests used in the establishment of lung cancer diagnosis and prognosis, in their laboratories"--Publisher's description
备用描述
"This detailed book serves as a laboratory manual containing vital protocols and in-depth discussion involving commonly used experimental approaches for the characterization of several aspects of lung tumor biology. Beginning with an extensive section on biomarker detection, the volume continues with chapters on the genetic and molecular characterization of lung cancer biological samples as well as protocols for the generation of research tools and pre-clinical lung cancer models. Written for the highly successful Methods in Molecular Biology series, chapters include introductions to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible protocols, and tips on troubleshooting and avoiding known pitfalls. Authoritative and practical, Lung Cancer: Methods and Protocols provides a global perspective of research efforts related to lung cancer, while allowing researchers to experimentally probe the different aspects of lung cancer research, including the experimentally relevant tests used in the establishment of lung cancer diagnosis and prognosis, in their laboratories"--Résumés de l'éditeur
开源日期
2021-03-10
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- 低速服务器(合作方提供) #1 (稍快但需要排队)
- 低速服务器(合作方提供) #2 (稍快但需要排队)
- 低速服务器(合作方提供) #3 (稍快但需要排队)
- 低速服务器(合作方提供) #4 (稍快但需要排队)
- 低速服务器(合作方提供) #5 (无需排队,但可能非常慢)
- 低速服务器(合作方提供) #6 (无需排队,但可能非常慢)
- 低速服务器(合作方提供) #7 (无需排队,但可能非常慢)
- 低速服务器(合作方提供) #8 (无需排队,但可能非常慢)
- 低速服务器(合作方提供) #9 (无需排队,但可能非常慢)
- 下载后: 在我们的查看器中打开
所有选项下载的文件都相同,应该可以安全使用。即使这样,从互联网下载文件时始终要小心。例如,确保您的设备更新及时。
外部下载
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对于大文件,我们建议使用下载管理器以防止中断。
推荐的下载管理器:JDownloader -
您将需要一个电子书或 PDF 阅读器来打开文件,具体取决于文件格式。
推荐的电子书阅读器:Anna的档案在线查看器、ReadEra和Calibre -
使用在线工具进行格式转换。
推荐的转换工具:CloudConvert和PrintFriendly -
您可以将 PDF 和 EPUB 文件发送到您的 Kindle 或 Kobo 电子阅读器。
推荐的工具:亚马逊的“发送到 Kindle”和djazz 的“发送到 Kobo/Kindle” -
支持作者和图书馆
✍️ 如果您喜欢这个并且能够负担得起,请考虑购买原版,或直接支持作者。
📚 如果您当地的图书馆有这本书,请考虑在那里免费借阅。
下面的文字仅以英文继续。
总下载量:
“文件的MD5”是根据文件内容计算出的哈希值,并且基于该内容具有相当的唯一性。我们这里索引的所有影子图书馆都主要使用MD5来标识文件。
一个文件可能会出现在多个影子图书馆中。有关我们编译的各种数据集的信息,请参见数据集页面。
有关此文件的详细信息,请查看其JSON 文件。 Live/debug JSON version. Live/debug page.