scholarly journals Correction: Targeting immunogenic cancer cell death by photodynamic therapy: past, present and future

2021 ◽  
Vol 9 (10) ◽  
pp. e001926corr1
2019 ◽  
Vol 24 (11) ◽  
pp. 1 ◽  
Author(s):  
Jingjing Lu ◽  
Bhaskar Roy ◽  
Marlys Anderson ◽  
Cadman L. Leggett ◽  
Michael J. Levy ◽  
...  

2009 ◽  
Vol 280 (1) ◽  
pp. 101-109 ◽  
Author(s):  
Bartosz Ferens ◽  
Anna Kawiak ◽  
Bogdan Banecki ◽  
Krzysztof P. Bielawski ◽  
Joanna Zawacka-Pankau

Nanomaterials ◽  
2018 ◽  
Vol 8 (9) ◽  
pp. 658 ◽  
Author(s):  
Rachel Riley ◽  
Rachel O’Sullivan ◽  
Andrea Potocny ◽  
Joel Rosenthal ◽  
Emily Day

Light-activated therapies are ideal for treating cancer because they are non-invasive and highly specific to the area of light application. Photothermal therapy (PTT) and photodynamic therapy (PDT) are two types of light-activated therapies that show great promise for treating solid tumors. In PTT, nanoparticles embedded within tumors emit heat in response to laser light that induces cancer cell death. In PDT, photosensitizers introduced to the diseased tissue transfer the absorbed light energy to nearby ground state molecular oxygen to produce singlet oxygen, which is a potent reactive oxygen species (ROS) that is toxic to cancer cells. Although PTT and PDT have been extensively evaluated as independent therapeutic strategies, they each face limitations that hinder their overall success. To overcome these limitations, we evaluated a dual PTT/PDT strategy for treatment of triple negative breast cancer (TNBC) cells mediated by a powerful combination of silica core/gold shell nanoshells (NSs) and palladium 10,10-dimethyl-5,15-bis(pentafluorophenyl)biladiene-based (Pd[DMBil1]-PEG750) photosensitizers (PSs), which enable PTT and PDT, respectively. We found that dual therapy works synergistically to induce more cell death than either therapy alone. Further, we determined that low doses of light can be applied in this approach to primarily induce apoptotic cell death, which is vastly preferred over necrotic cell death. Together, our results show that dual PTT/PDT using silica core/gold shell NSs and Pd[DMBil1]-PEG750 PSs is a comprehensive therapeutic strategy to non-invasively induce apoptotic cancer cell death.


2015 ◽  
Vol 14 (8) ◽  
pp. 1410-1424 ◽  
Author(s):  
Abhishek D. Garg ◽  
Hannelore Maes ◽  
Erminia Romano ◽  
Patrizia Agostinis

Autophagy is fundamentally a cytoprotective and pro-survival process yet studies have shown that it has an exceedingly contextual role in cancer biology; depending on the phase, location or type of oncogenic trigger and/or therapy, its role could fluctuate from pro- to anti-tumourigenic.


2016 ◽  
Vol 61 ◽  
pp. S115
Author(s):  
N. Almeida ◽  
M. Laranjo ◽  
A. Serra ◽  
M. Abrantes ◽  
M. Pineiro ◽  
...  

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