TY - JOUR
T1 - Trial Watch
T2 - Immunogenic cell death inducers for anticancer chemotherapy
AU - Pol, Jonathan
AU - Vacchelli, Erika
AU - Aranda, Fernando
AU - Castoldi, Francesca
AU - Eggermont, Alexander
AU - Cremer, Isabelle
AU - Sautès-Fridman, Catherine
AU - Fucikova, Jitka
AU - Galon, Jérôme
AU - Spisek, Radek
AU - Tartour, Eric
AU - Zitvogel, Laurence
AU - Kroemer, Guido
AU - Galluzzi, Lorenzo
N1 - Publisher Copyright:
© 2015 Taylor & Francis Group, LLC.
PY - 2015/1/1
Y1 - 2015/1/1
N2 - The term “immunogenic cell death” (ICD) is now employed to indicate a functionally peculiar form of apoptosis that is sufficient for immunocompetent hosts to mount an adaptive immune response against dead cell-associated antigens. Several drugs have been ascribed with the ability to provoke ICD when employed as standalone therapeutic interventions. These include various chemotherapeutics routinely employed in the clinic (e.g., doxorubicin, epirubicin, idarubicin, mitoxantrone, bleomycin, bortezomib, cyclophosphamide and oxaliplatin) as well as some anticancer agents that are still under preclinical or clinical development (e.g., some microtubular inhibitors of the epothilone family). In addition, a few drugs are able to convert otherwise non-immunogenic instances of cell death into bona fide ICD, and may therefore be employed as chemotherapeutic adjuvants within combinatorial regimens. This is the case of cardiac glycosides, like digoxin and digitoxin, and zoledronic acid. Here, we discuss recent developments on anticancer chemotherapy based on ICD inducers.
AB - The term “immunogenic cell death” (ICD) is now employed to indicate a functionally peculiar form of apoptosis that is sufficient for immunocompetent hosts to mount an adaptive immune response against dead cell-associated antigens. Several drugs have been ascribed with the ability to provoke ICD when employed as standalone therapeutic interventions. These include various chemotherapeutics routinely employed in the clinic (e.g., doxorubicin, epirubicin, idarubicin, mitoxantrone, bleomycin, bortezomib, cyclophosphamide and oxaliplatin) as well as some anticancer agents that are still under preclinical or clinical development (e.g., some microtubular inhibitors of the epothilone family). In addition, a few drugs are able to convert otherwise non-immunogenic instances of cell death into bona fide ICD, and may therefore be employed as chemotherapeutic adjuvants within combinatorial regimens. This is the case of cardiac glycosides, like digoxin and digitoxin, and zoledronic acid. Here, we discuss recent developments on anticancer chemotherapy based on ICD inducers.
KW - Antigen-presenting cell
KW - Autophagy
KW - Damage-associated molecular pattern
KW - Dendritic cell
KW - Endoplasmic reticulum stress
KW - Type I interferon
UR - http://www.scopus.com/inward/record.url?scp=84942375939&partnerID=8YFLogxK
U2 - 10.1080/2162402X.2015.1008866
DO - 10.1080/2162402X.2015.1008866
M3 - Article
AN - SCOPUS:84942375939
SN - 2162-4011
VL - 4
JO - OncoImmunology
JF - OncoImmunology
IS - 4
ER -