Human astrocytes and astrocytoma respond differently to resveratrol

被引:3
|
作者
Gran, Evan Rizzel [1 ]
Lotocki, Victor [2 ,4 ]
Zhang, Qiaochu [1 ,2 ]
Antel, Jack [3 ]
Kakkar, Ashok [2 ]
Maysinger, Dusica [1 ]
机构
[1] McGill Univ, Dept Pharmacol & Therapeut, Montreal, PQ, Canada
[2] McGill Univ, Dept Chem, Montreal, PQ, Canada
[3] McGill Univ, Montreal Neurol Inst, Neuroimmunol Unit, Montreal, PQ H3A 2B4, Canada
[4] Univ Toronto, Dept Chem, Toronto, ON, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Resveratrol; Glutathione; Reactive oxygen species; Astrocytes; Astrocytoma; Miktoarm polymers; GLUTATHIONE CONTENT; LOADING EFFICIENCY; GLIOBLASTOMA CELLS; TEMOZOLOMIDE; NANOPARTICLES; ANTIOXIDANT; DOXORUBICIN; STABILITY; CULTURES; NEURONS;
D O I
10.1016/j.nano.2021.102441
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
A fundamental problem in oncology is that anticancer chemotherapeutics kill both cancer and healthy cells in the surrounding tissues. Resveratrol is a natural antioxidant with intriguing and opposing biological properties: it reduces viability of some cancer cells but not of non-transformed ones (in equimolar concentrations). Therefore, we examined resveratrol in human non-transformed primary astrocytes and astrocytoma. Resveratrol reduced reactive oxygen species in astrocytes, but not in astrocytoma. Such cell-type dependent response is particularly evident with analyses at the single cell level showing clear population difference in high and low glutathione levels. Due to resveratrol's poor aqueous solubility that limits its use in clinics, we incorporated it into stimulus-responsive micelles assembled from miktoarm polymers. This could be an attractive chemotherapeutic delivery strategy in nano-oncology. As a proof of principle, we show that these formulations containing resveratrol markedly decrease astrocytoma viability, particularly in combination with temozolomide, a first line chemotherapeutic for astrocytoma. (c) 2021 Elsevier Inc. All rights reserved.
引用
收藏
页数:12
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