Unravelling "off-target" effects of redox-active polymers and polymer multilayered capsules in prostate cancer cells

被引:9
作者
Beretta, Giovanni L. [1 ]
Folini, Marco [1 ]
Cavalieri, Francesca [2 ,3 ,4 ]
Yan, Yan [3 ,4 ]
Fresch, Enrico [2 ]
Kaliappan, Subramanian [2 ]
Hasenhoerl, Christoph [5 ]
Richardson, Joseph J. [3 ,4 ]
Tinelli, Stella [1 ]
Fery, Andreas [5 ]
Caruso, Frank [3 ,4 ]
Zaffaroni, Nadia [1 ]
机构
[1] Fdn IRCCS Ist Nazl Tumori, Dept Expt Oncol & Mol Med, I-20133 Milan, Italy
[2] Univ Roma Tor Vergata, Dipartimento Sci & Tecnol Chim, I-00173 Rome, Italy
[3] Univ Melbourne, ARC Ctr Excellence Convergent Bionano Sci & Techn, Parkville, Vic 3010, Australia
[4] Univ Melbourne, Dept Chem & Biomol Engn, Parkville, Vic 3010, Australia
[5] Univ Bayreuth, Dept Phys Chem 2, D-95440 Bayreuth, Germany
基金
澳大利亚研究理事会;
关键词
HYDROGEL CAPSULES; DRUG-DELIVERY; DNA-DAMAGE; AUTOPHAGY; NANOPARTICLES; ENDOCYTOSIS; MECHANISMS; CARRIERS; DEATH;
D O I
10.1039/c4nr07240e
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
Redox-active polymers and carriers are oxidizing nanoagents that can potentially trigger intracellular off-target effects. In the present study, we investigated the occurrence of off-target effects in prostate cancer cells following exposure to redox-active polymer and thin multilayer capsules with different chemical properties. We show that, depending on the intracellular antioxidant capacity, thiol-functionalized poly(methacrylic acid), PMASH triggers cell defense responses/perturbations that result in off-target effects (i.e., induction of autophagy and down-regulation of survivin). Importantly, the conversion of the carboxyl groups of PMASH into the neutral amides of poly(hydroxypropylmetacrylamide) (pHPMASH) nullified the off-target effects and cytotoxicity in tested cell lines. This suggests that the simultaneous action of carboxyl and disulfide groups in PMASH polymer or capsules may play a role in mediating the intracellular off-target effects. Our work provides evidence that the rational design of redox-active carriers for therapeutic-related application should be guided by a careful investigation on potential disturbance of the cellular machineries related to the carrier association.
引用
收藏
页码:6261 / 6270
页数:10
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