International Review of Cell and Molecular Biology ( Volume 331 )

Publication series :Volume 331

Author: Galluzzi   Lorenzo  

Publisher: Elsevier Science‎

Publication year: 2017

E-ISBN: 9780128124703

P-ISBN(Paperback): 9780128124697

Subject: Q2 Cytobiology

Keyword: 分子生物学,细胞生物学

Language: ENG

Access to resources Favorite

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Description

International Review of Cell and Molecular Biology reviews and details current advances in cell and molecular biology. This most current release in this highly cited series focuses on such timely topics as novel treatments in immunotherapy in breast cancer, chemokine receptor signaling and the hallmarks of cancer, tumor-targeting antibodies, and a section on mitochondrion and whether they are a common organelle for cell death. As always, readers will find the articles in this series to be of great value, with a high impact and average cited half-life of nine years.

The IRCMB series has a worldwide readership, maintaining a high standard by publishing invited articles on important and timely topics that are authored by prominent cell and molecular biologists. This great resource ranks high amongst scientific journals dealing with cell biology.

  • Publishes only invited review articles on selected topics
  • Authored by established and active cell and molecular biologists, drawn from international sources
  • Offers a wide range of perspectives on specific subjects

Chapter

3. Immune System in the Therapeutic Response in BC. The Immunogenic Cell Death

4. T-Infiltrating Lymphocytes Molecular and Genomic Characterization as a Strategic Tool to Better Understand BC Behavior

5. Neoantigen Prediction: Genomic Tools for Personalized Immunotherapy

6. Immunotherapeutic Approaches in BC. Clinical Trials With Immune Checkpoint Inhibitors

6.1. Early Results in Clinical Trials With Immune Checkpoints as Single Therapy

6.1.1. A Phase Ib Multicohort Study of MK-3475 in Subjects With Advanced Solid Tumors (Keynote-012). NCI01848834

6.1.2. Phase IB Study of MK-3475 in Subjects With Select Advanced Solid Tumors (Keynote-028). NCT02054806

6.1.3. A Phase I, Open-Label, Dose Escalation Study of the Safety and Pharmacokinetics of Atezolizumab Administered Intra ...

6.2. Early Results in Clinical Trials With Immune Checkpoints in the Context of Combinations

6.2.1. A Phase Ib Study of the Safety and Pharmacology of Atezolizumab Administered With Bevacizumab and/or With Chemothe ...

6.3. Ongoing and Planned Clinical Trials With Immune Checkpoints Inhibitors in BC

7. Conclusions

Acknowledgments

References

Chapter Two: New Insights Into Cellular Stress Responses to Environmental Metal Toxicants

1. Introduction

2. ER Stress and UPR

2.1. Activation of UPR Signaling

2.1.1. IRE1 Signaling

2.1.2. PERK Signaling

2.1.3. ATF6 Signaling

2.2. ER Stress-Induced Apoptosis

3. Metal-Induced ER Stress

3.1. Mechanisms of Metal-Induced ER Stress

3.2. Metal-Induced ER Stress and Human Disease

3.2.1. Arsenic-Induced ER Stress in Metabolic Diseases

3.2.2. Cadmium Nephrotoxicity and ER Stress

3.2.3. Lead Neurotoxicity and ER Stress

3.2.4. Manganese (Mn) and Neurotoxicity

4. ER Stress and Its Impact on Oxidative Stress

4.1. ROS Formation in Mitochondria

4.2. ROS Formation by Oxidative Protein Folding in ER

4.3. Interplay Between Oxidative Stress and ER Stress

5. Genomics Approaches in Metal-Induced Cell Stress Studies

5.1. RNA Sequencing

5.2. Functional Genomic Screening

5.2.1. RNA Interference

5.2.2. CRISPR/Cas9 Functional Screening

6. Conclusions and Future Directions

Acknowledgments

References

Chapter Three: An Update on Src Family of Nonreceptor Tyrosine Kinases Biology

1. Introduction

2. Regulation of SFKs Function

3. Redox-Dependent Regulation of SFK Function

4. Role of SFKs in PRL Signaling

5. Relevance of SFKs in Breast Cancer

5.1. SFKs and Breast Cancer Stem Cells

6. Role of SFKs During Mammalian Embryo Development and in the Regulation of Embryonic and Somatic Stem Cells

7. Conclusions

Acknowledgments

References

Chapter Four: STAT Transcription Factors in T Cell Control of Health and Disease

1. Engagement of the Jak-STAT Signaling Pathway

2. Jak-STAT Molecules in T Helper Cell Differentiation

2.1. Th1 Cells

2.2. Th2 Cells

2.3. Th17 Cells

2.4. Treg Cells

2.5. Tfh Cells

2.6. Th9 Cells

3. STAT Molecules in the Development of Cytotoxic T Cells

3.1. Tc1 Cells

3.2. Tc2 Cells

3.3. Tc17 Cells

3.4. Tc9 Cells

4. STATs Mutations Result in Patient Immunodeficiency

5. STAT Molecules in Allergic Inflammation

5.1. Jak Proteins in Allergic Inflammation

5.2. STAT1

5.3. STAT3

5.4. STAT4

5.5. STAT5

5.6. STAT6

6. Role of STAT Molecules in Intestinal Inflammation

6.1. STAT1

6.2. STAT3

6.3. STAT4

6.4. STAT5

6.5. STAT6

7. Jak-STAT Molecules in Autoimmune Diseases

7.1. STAT1

7.2. STAT3

7.3. STAT4

7.4. STAT5

7.5. STAT6

8. Blocking Cytokine Signaling to Treat Disease

8.1. STAT1 Inhibitor

8.2. STAT3 Inhibitor

8.3. STAT4 Inhibitor

8.4. STAT5 Inhibitor

8.5. STAT6 Inhibitor

9. Conclusion

References

Chapter Five: Chemokine Receptor Signaling and the Hallmarks of Cancer

1. Introduction

2. The Chemokine Superfamily

2.1. Chemokines, the Ligands

2.2. Signal Transduction by Chemokine Receptors

3. Chemokine Activity on Neoplastic Cells

3.1. Chemokine Signaling Sustains Tumor Cell Proliferation

3.2. Chemokines Interact With Tumor Suppressor Genes

3.3. Chemokines as Regulators of Apoptosis in Cancer Cells

3.4. Chemokines as Drivers and Cues for Tumor Invasion and Metastasis

3.5. Chemokines and Cancer Stem Cell Plasticity

4. Chemokine Activities on Stromal Cells

4.1. Chemokines as Positive and Negative Regulators of Tumor Vascularization

4.2. Chemokines as Shapers of the Tumor Inflammatory Milieu

5. Concluding Remarks

Acknowledgments

References

Chapter Six: Mitochondrion: A Common Organelle for Distinct Cell Deaths?

1. Introduction

2. Apoptosis

2.1. Extrinsic Apoptosis

2.2. Intrinsic Apoptosis

3. MPT-Driven Necrosis

4. Mitophagy

4.1. Introduction and Molecular Mechanisms

4.2. Mitophagy and Cell Death

4.3. Mitophagy, Cytoprotection, and Mitochondrial Quality Control

5. Implication of Mitophagy in Models of Neurological Diseases

6. Implication of Mitochondria-Dependent Cell Death in Cardiac Diseases

6.1. Outer Membrane Proteins

6.2. Intermembrane Space Proteins

6.3. Inner Membrane Proteins

6.4. Matrix Proteins

7. Conclusion and Perspectives

Acknowledgments

References

Chapter Seven: Antibody-Based Cancer Therapy: Successful Agents and Novel Approaches

1. Introduction

2. Monoclonal Antibodies

3. Effector Mechanisms and Activity of Tumor-Targeting Antibodies

3.1. Antibody-Dependent Cellular Cytotoxicity

3.2. Antibody-Dependent Cellular Phagocytosis

3.3. Complement-Dependent Cytotoxicity

3.4. Signaling Modulation

3.5. Clinical Experience

4. Immunomodulatory Antibodies

4.1. Checkpoint Blocking mAbs

4.2. Immunostimulatory mAbs That Target the TNFR Superfamily

5. Antibody Engineering to Improve Effector Functions

5.1. Isotype Selection

5.2. Amino Acid Sequence Modifications

5.3. N-Glycan Structure Modification

6. Alternative Antibody Formats

6.1. Antigen-Binding Fragments

6.2. Bispecific Antibodies

6.2.1. Immune-Retargeting bsAbs

6.2.2. Direct Tumor Targeting With bsAbs

7. Antibody-Drug Conjugates

7.1. Chemotherapeutics

7.1.1. Improvement Strategies for ADCs

7.2. Toxins

8. Antibody-Cytokine Fusion Proteins

8.1. Interferons

8.2. Interleukins

8.3. TNF Superfamily Ligands

8.3.1. TNF-related apoptosis-inducing ligand

8.3.2. CD40/CD40L

8.3.3. 4-1BB/4-1BBL

9. CAR-Transfected T Cells

10. Conclusions

References

Back Cover

The users who browse this book also browse