Immunogenic Cell Death, DAMPs and Prothymosin α as a Putative Anticancer Immune Response Biomarker.
Anastasios I BirmpilisAntonios PaschalisApostolis MourkakisPanayiota ChristodoulouIoannis V KostopoulosElina AntimissariGeorgia I TerzoudiAlexandros G GeorgakilasChristina ArmpiliaPanagiotis PapageorgisEfstathios KastritisEvangelos TerposMeletios- Athanasios DimopoulosHubert KalbacherEvangelia LivaniouMaria-Ioanna ChristodoulouOurania E TsitsilonisPublished in: Cells (2022)
The new and increasingly studied concept of immunogenic cell death (ICD) revealed a previously unknown perspective of the various regulated cell death (RCD) modalities, elucidating their immunogenic properties and rendering obsolete the notion that immune stimulation is solely the outcome of necrosis. A distinct characteristic of ICD is the release of danger-associated molecular patterns (DAMPs) by dying and/or dead cells. Thus, several members of the DAMP family, such as the well-characterized heat shock proteins (HSPs) HSP70 and HSP90, the high-mobility group box 1 protein and calreticulin, and the thymic polypeptide prothymosin α (proTα) and its immunoreactive fragment proTα(100-109), are being studied as potential diagnostic tools and/or possible therapeutic agents. Here, we present the basic aspects and mechanisms of both ICD and other immunogenic RCD forms; denote the role of DAMPs in ICD; and further exploit the relevance of human proTα and proTα(100-109) in ICD, highlighting their possible clinical applications. Furthermore, we present the preliminary results of our in vitro studies, which show a direct correlation between the concentration of proTα/proTα(100-109) and the levels of cancer cell apoptosis, induced by anticancer agents and γ-radiation.
Keyphrases
- heat shock
- cell death
- cell cycle arrest
- heat shock protein
- heat stress
- immune response
- endothelial cells
- induced apoptosis
- oxidative stress
- cell proliferation
- squamous cell carcinoma
- papillary thyroid
- risk assessment
- single molecule
- squamous cell
- amino acid
- solid state
- induced pluripotent stem cells
- signaling pathway