TY - JOUR
T1 - The therapeutic effect of death
T2 - Newcastle disease virus and its antitumor potential
AU - Cuadrado-Castano, Sara
AU - Sanchez-Aparicio, Maria T.
AU - García-Sastre, Adolfo
AU - Villar, Enrique
N1 - Funding Information:
Work on NDV vectors in the AG-S laboratory is partially supported by NIAID grant R01AI088770 .
Publisher Copyright:
© 2015 Elsevier B.V.
PY - 2015/11/2
Y1 - 2015/11/2
N2 - Programmed cell death is essential to survival of multicellular organisms. Previously restricted to apoptosis, the concept of programmed cell death is now extended to other mechanisms, as programmed necrosis or necroptosis, autophagic cell death, pyroptosis and parthanatos, among others. Viruses have evolved to manipulate and take control over the programmed cell death response, and the infected cell attempts to neutralize viral infections displaying different stress signals and defensive pathways before taking the critical decision of self-destruction. Learning from viruses and their interplay with the host may help us to better understand the complexity of the self-defense death response that when altered might cause disorders as important as cancer. In addition, as the fields of immunotherapy and oncolytic viruses advance as promising novel cancer therapies, the programmed cell death response reemerges as a key point for the success of both therapeutic approaches. In this review we summarize the research of the multimodal cell death response induced by Newcastle disease viruses (NDV), considered nowadays a promising viral oncolytic therapeutic, and how the manipulation of the host programmed cell death response can enhance the NDV antitumor capacity.
AB - Programmed cell death is essential to survival of multicellular organisms. Previously restricted to apoptosis, the concept of programmed cell death is now extended to other mechanisms, as programmed necrosis or necroptosis, autophagic cell death, pyroptosis and parthanatos, among others. Viruses have evolved to manipulate and take control over the programmed cell death response, and the infected cell attempts to neutralize viral infections displaying different stress signals and defensive pathways before taking the critical decision of self-destruction. Learning from viruses and their interplay with the host may help us to better understand the complexity of the self-defense death response that when altered might cause disorders as important as cancer. In addition, as the fields of immunotherapy and oncolytic viruses advance as promising novel cancer therapies, the programmed cell death response reemerges as a key point for the success of both therapeutic approaches. In this review we summarize the research of the multimodal cell death response induced by Newcastle disease viruses (NDV), considered nowadays a promising viral oncolytic therapeutic, and how the manipulation of the host programmed cell death response can enhance the NDV antitumor capacity.
KW - Apoptosis
KW - Autophagy
KW - Necroptosis
KW - Newcastle disease virus
KW - Oncolytic virus
KW - Programmed cell death
KW - Recombinant virus
KW - Tumor therapy
UR - http://www.scopus.com/inward/record.url?scp=84959456037&partnerID=8YFLogxK
U2 - 10.1016/j.virusres.2015.07.001
DO - 10.1016/j.virusres.2015.07.001
M3 - Review article
C2 - 26221764
AN - SCOPUS:84959456037
SN - 0168-1702
VL - 209
SP - 56
EP - 66
JO - Virus Research
JF - Virus Research
ER -