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Stress-induced cellular responses in immunogenic cell death: Implications for cancer immunotherapy.
- Source :
-
Biochemical pharmacology [Biochem Pharmacol] 2018 Jul; Vol. 153, pp. 12-23. Date of Electronic Publication: 2018 Feb 10. - Publication Year :
- 2018
-
Abstract
- Cancer is evading the host's defense mechanisms leading to avoidance of immune destruction. During tumor progression, immune-evading cancer cells arise due to selective pressure from the hypoxic and nutrient-deprived microenvironment. Thus, therapies aiming at re-establishing immune destruction of pathological cells constitute innovating anti-cancer strategies. Accumulating evidence suggests that selected conventional chemotherapeutic drugs increase the immunogenicity of stressed and dying cancer cells by triggering a form of cell death called immunogenic cell death (ICD), which is characterized by the release of danger-associated molecular patterns (DAMPs). In this review, we summarize the effects of ICD inducers on DAMP signaling leading to adjuvanticity and antigenicity. We will discuss the associated stress response pathways that cause the release of DAMPs leading to improved immune recognition and their relevance in cancer immunotherapy. Our aim is to highlight the contribution of adaptive immunity to the long-term clinical benefits of anticancer treatments and the properties of immune memory that can protect cancer patients against relapse.<br /> (Copyright © 2018. Published by Elsevier Inc.)
- Subjects :
- Animals
Cell Death drug effects
Cell Death immunology
Endoplasmic Reticulum Stress drug effects
Endoplasmic Reticulum Stress immunology
Humans
Immunity, Cellular drug effects
Immunogenetic Phenomena drug effects
Immunogenetic Phenomena physiology
Signal Transduction drug effects
Signal Transduction immunology
Stress, Physiological drug effects
Immunity, Cellular immunology
Immunotherapy methods
Neoplasms immunology
Neoplasms therapy
Stress, Physiological immunology
Subjects
Details
- Language :
- English
- ISSN :
- 1873-2968
- Volume :
- 153
- Database :
- MEDLINE
- Journal :
- Biochemical pharmacology
- Publication Type :
- Academic Journal
- Accession number :
- 29438676
- Full Text :
- https://doi.org/10.1016/j.bcp.2018.02.006