TY - JOUR
T1 - Immunogenicity of anthracyclines
T2 - moving towards more personalized medicine
AU - Apetoh, Lionel
AU - Mignot, Grégoire
AU - Panaretakis, Theocharis
AU - Kroemer, Guido
AU - Zitvogel, Laurence
N1 - Funding Information:
L.A. received grants from Ligue contre le cancer and Fondation pour la recherche médicale (FRM) and G.M. from Association pour la Recherche sur le Cancer. L.Z. is supported by grants from Institut National contre le Cancer (INCa) and from European DC THERA, and G.K. is supported by a special grant from Ligue contre le Cancer (équipe labellisée), and by grants from the European Commission (Active p53, RIGHT, Trans-Death, Death-Train, ChemoRes, INCa, Cancéropôle Ile-de-France and the Association for International Cancer Research).
PY - 2008/4/1
Y1 - 2008/4/1
N2 - The current method of cancer management takes into account tumor-related factors to predict therapeutic outcome. However, recent evidence indicates that the host immune system also contributes to therapeutic outcome. Here, we highlight anthracyclines, which have been used to treat a broad range of cancers since the 1960s, as an example of an anticancer treatment that can boost the host's immune system to improve the efficacy of chemotherapy. It has recently been revealed that the translocation of calreticulin to the plasma membrane in tumor cells and the release of high-mobility-group box 1 (HMGB1) by tumor cells are two key post-transcriptional events required for the immunogenicity of anthracyclines. These discoveries represent a conceptual advance in the understanding of the mechanisms underlying the immunogenicity of anthracyclines. We review the effects of anthracyclines on the host immune system and discuss how this knowledge can be exploited for anticancer therapy.
AB - The current method of cancer management takes into account tumor-related factors to predict therapeutic outcome. However, recent evidence indicates that the host immune system also contributes to therapeutic outcome. Here, we highlight anthracyclines, which have been used to treat a broad range of cancers since the 1960s, as an example of an anticancer treatment that can boost the host's immune system to improve the efficacy of chemotherapy. It has recently been revealed that the translocation of calreticulin to the plasma membrane in tumor cells and the release of high-mobility-group box 1 (HMGB1) by tumor cells are two key post-transcriptional events required for the immunogenicity of anthracyclines. These discoveries represent a conceptual advance in the understanding of the mechanisms underlying the immunogenicity of anthracyclines. We review the effects of anthracyclines on the host immune system and discuss how this knowledge can be exploited for anticancer therapy.
UR - http://www.scopus.com/inward/record.url?scp=41549145181&partnerID=8YFLogxK
U2 - 10.1016/j.molmed.2008.02.002
DO - 10.1016/j.molmed.2008.02.002
M3 - Review article
C2 - 18353726
AN - SCOPUS:41549145181
SN - 1471-4914
VL - 14
SP - 141
EP - 151
JO - Trends in Molecular Medicine
JF - Trends in Molecular Medicine
IS - 4
ER -