4.6 Article

Image-guided photo-therapeutic nanoporphyrin synergized HSP90 inhibitor in patient-derived xenograft bladder cancer model

Journal

NANOMEDICINE-NANOTECHNOLOGY BIOLOGY AND MEDICINE
Volume 14, Issue 3, Pages 789-799

Publisher

ELSEVIER
DOI: 10.1016/j.nano.2017.12.014

Keywords

Photodynamic therapy; Photothermal therapy; HSP90 inhibitor; Bladder cancer; Nanoparticle

Funding

  1. NIH/NCI [R01CA199668]
  2. NIH/NICHD [R01HD086195]
  3. DoD PRMRP Award [PR121626]
  4. Cancer Center Support Grant [P30 CA093373]
  5. ACS IRG
  6. VA BLR&D Merit grant from the United States (U.S.) Department of Veterans Affairs Biomedical Laboratory Research and Development Program [1I01BX001784]
  7. EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT [R01HD086195] Funding Source: NIH RePORTER
  8. NATIONAL CANCER INSTITUTE [R01CA176803, R01CA199668, K12CA138464, P30CA093373] Funding Source: NIH RePORTER
  9. Veterans Affairs [I01BX001784] Funding Source: NIH RePORTER

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Photodynamic therapy is a promising and effective non-invasive therapeutic approach for the treatment of bladder cancers. Therapies targeting HSP90 have the advantage of tumor cell selectivity and have shown great preclinical efficacy. In this study, we evaluated a novel multifunctional nanoporphyrin platform loaded with an HSP90 inhibitor 17AAG (NP-AAG) for use as a multi-modality therapy against bladder cancer. NP-AAG was efficiently accumulated and retained at bladder cancer patient-derived xenograft (PDX) over 7 days. PDX tumors could be synergistically eradicated with a single intravenous injection ofNP-AAGfollowed bymultiple light treatments within 7 days. NP-AAGmediated treatment could not only specifically deliver 17AAG and produce heat and reactive oxygen species, but also more effectively inhibit essential bladder cancer essential signaling molecules like Akt, Src, and Erk, as well as HIF-1 alpha induced by photo-therapy. This multifunctional nanoplatform has high clinical relevance and could dramatically improve management for bladder cancers with minimal toxicity. (c) 2018 Elsevier Inc. All rights reserved.

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