TY - JOUR
T1 - Association of oncolytic adenoviruses with chemotherapies
T2 - An overview and future directions
AU - Bressy, Christian
AU - Benihoud, Karim
N1 - Funding Information:
This work was supported by the Centre National de la Recherche Scientifique , the University Paris-Sud , the INCa (PIMRANIS project) and EDF . C.B. received a fellowship from the Ministère de la Recherche et de la Technologie. The authors want to acknowledge Najat Raddi for her critical reading of the manuscript.
PY - 2014/7/15
Y1 - 2014/7/15
N2 - Oncolytic adenoviruses have been used in different preclinical and clinical studies, showing their capacity to kill tumor cells without major adverse events. However, these studies also underline the limitations of this approach. The efficacy of oncolytic adenoviruses is hampered by their limited ability to transduce some tumor types, their lack of selectivity, and their poor dissemination within tumors. In addition, the host immune response may limit oncolytic adenovirus efficacy. Combining oncolytic adenoviruses with chemotherapeutics constitutes an appealing strategy to increase their potency. The first part of this review describes the molecular basis of oncolytic adenoviruses, their use in preclinical studies and clinical trials, their limitations, and strategies to circumvent these limitations. The second part will focus on studies combining oncolytic adenoviruses with chemotherapeutic drugs, including standard chemotherapeutic drugs, molecularly targeted drugs, and other drugs that have been combined with oncolytic adenoviruses. Finally, based on these studies, we describe future directions and general rules that could be followed to identify chemotherapeutic drugs displaying additive/synergistic effects when combined with oncolytic adenoviruses.
AB - Oncolytic adenoviruses have been used in different preclinical and clinical studies, showing their capacity to kill tumor cells without major adverse events. However, these studies also underline the limitations of this approach. The efficacy of oncolytic adenoviruses is hampered by their limited ability to transduce some tumor types, their lack of selectivity, and their poor dissemination within tumors. In addition, the host immune response may limit oncolytic adenovirus efficacy. Combining oncolytic adenoviruses with chemotherapeutics constitutes an appealing strategy to increase their potency. The first part of this review describes the molecular basis of oncolytic adenoviruses, their use in preclinical studies and clinical trials, their limitations, and strategies to circumvent these limitations. The second part will focus on studies combining oncolytic adenoviruses with chemotherapeutic drugs, including standard chemotherapeutic drugs, molecularly targeted drugs, and other drugs that have been combined with oncolytic adenoviruses. Finally, based on these studies, we describe future directions and general rules that could be followed to identify chemotherapeutic drugs displaying additive/synergistic effects when combined with oncolytic adenoviruses.
KW - CRAd
KW - Chemotherapeutic
KW - Oncolytic adenoviruses
UR - http://www.scopus.com/inward/record.url?scp=84902247576&partnerID=8YFLogxK
U2 - 10.1016/j.bcp.2014.05.003
DO - 10.1016/j.bcp.2014.05.003
M3 - Comment/debate
C2 - 24832861
AN - SCOPUS:84902247576
SN - 0006-2952
VL - 90
SP - 97
EP - 106
JO - Biochemical Pharmacology
JF - Biochemical Pharmacology
IS - 2
ER -