TY - JOUR
T1 - Nanotechnology and immunotherapy in ovarian cancer
T2 - Tracing new landscapes
AU - Corradetti, Bruna
AU - Pisano, Simone
AU - Conlan, Robert Steven
AU - Ferrari, Mauro
N1 - Funding Information:
M.F. is supported through the National Institutes of Health National Cancer Institute [Grants U54CA210181 and R01CA222959], Department of Defense Breast Cancer Research Breakthrough Level IV Award [W81XWH-17-1-0389], and his Ernest Cockrell Jr. Presidential Distinguished Chair at Houston Methodist Research Institute. M.F. serves on the Board of Directors of Arrowhead Pharmaceuticals. B.C. is supported through the Sêr Cymru II programme, funded by the European Commission through the Horizon 2020 Marie Skłodowska-Curie Actions COFUND scheme and the Welsh European Funding Office under the European Regional Development Fund. S.P. is sponsored by the Swansea University (UK)/Houston Methodist Research Institute (US) Joint Initiative. https://doi.org/10.1124/jpet.118.254979.
Funding Information:
M.F. is supported through the National Institutes of Health National Cancer Institute [Grants U54CA210181 and R01CA222959], Department of Defense Breast Cancer Research Breakthrough Level IV Award [W81XWH-17-1-0389], and his Ernest Cockrell Jr. Presidential Distinguished Chair at Houston Methodist Research Institute. M.F. serves on the Board of Directors of Arrowhead Pharmaceuticals. B.C. is supported through the S?r Cymru II programme, funded by the European Commission through the Horizon 2020 Marie Sk?odowska-Curie Actions COFUND scheme and the Welsh European Funding Office under the European Regional Development Fund. S.P. is sponsored by the Swansea University (UK)/Houston Methodist Research Institute (US) Joint Initiative.
Publisher Copyright:
Copyright © 2019 by The American Society for Pharmacology and Experimental Therapeutics
PY - 2019
Y1 - 2019
N2 - Ovarian cancer (OC) is the seventh most common cancer in women worldwide. Standard therapeutic treatments involve debulking surgery combined with platinum-based chemotherapies. Of the patients with advanced-stage cancer who initially respond to current treatments, 50%-75% relapse. Immunotherapy-based approaches aimed at boosting antitumor immunity have recently emerged as promising tools to challenge tumor progression. Treatments with inhibitors of immune checkpoint molecules have shown impressive results in other types of tumors. However, only 15% of checkpoint inhibitors evaluated have proven successful in OC due to the immunosuppressive environment of the tumor and the transport barriers. This limits the efficacy of the existing immunotherapies. Nanotechnology-based delivery systems hold the potential to overcome such limitations. Various nanoformulations including polymeric, liposomes, and lipid-polymer hybrid nanoparticles have already been proposed to improve the biodistribution and targeting capabilities of drugs against tumor-associated immune cells, including dendritic cells and macrophages. In this review, we examine the impact of immunotherapeutic approaches that are currently under consideration for the treatment of OC. In this review, we also provide a comprehensive analysis of the existing nanoparticle-based synthetic strategies and their limitations and advantages over standard treatments. Furthermore, we discuss how the strength of the combination of nanotechnology with immunotherapy may help to overcome the current therapeutic limitations associated with their individual application and unravel a new paradigm in the treatment of this malignancy.
AB - Ovarian cancer (OC) is the seventh most common cancer in women worldwide. Standard therapeutic treatments involve debulking surgery combined with platinum-based chemotherapies. Of the patients with advanced-stage cancer who initially respond to current treatments, 50%-75% relapse. Immunotherapy-based approaches aimed at boosting antitumor immunity have recently emerged as promising tools to challenge tumor progression. Treatments with inhibitors of immune checkpoint molecules have shown impressive results in other types of tumors. However, only 15% of checkpoint inhibitors evaluated have proven successful in OC due to the immunosuppressive environment of the tumor and the transport barriers. This limits the efficacy of the existing immunotherapies. Nanotechnology-based delivery systems hold the potential to overcome such limitations. Various nanoformulations including polymeric, liposomes, and lipid-polymer hybrid nanoparticles have already been proposed to improve the biodistribution and targeting capabilities of drugs against tumor-associated immune cells, including dendritic cells and macrophages. In this review, we examine the impact of immunotherapeutic approaches that are currently under consideration for the treatment of OC. In this review, we also provide a comprehensive analysis of the existing nanoparticle-based synthetic strategies and their limitations and advantages over standard treatments. Furthermore, we discuss how the strength of the combination of nanotechnology with immunotherapy may help to overcome the current therapeutic limitations associated with their individual application and unravel a new paradigm in the treatment of this malignancy.
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U2 - 10.1124/jpet.118.254979
DO - 10.1124/jpet.118.254979
M3 - Review article
C2 - 30737357
AN - SCOPUS:85071488242
SN - 0022-3565
VL - 370
SP - 636
EP - 646
JO - Journal of Pharmacology and Experimental Therapeutics
JF - Journal of Pharmacology and Experimental Therapeutics
IS - 3
ER -