共 81 条
Redox resetting of cisplatin-resistant ovarian cancer cells by cisplatin-encapsulated nanostructured lipid carriers
被引:6
作者:
Mittal, Disha
[1
]
Biswas, Largee
[1
]
Verma, Anita Kamra
[1
]
机构:
[1] Univ Delhi, Dept Zool, Kirori Mal Coll, Nanobiotech Lab, Delhi 110007, India
关键词:
ATP7B;
cisplatin;
GSH;
nanostructured lipid carriers;
ovarian cancer;
reactive oxygen species;
redox resetting;
EFFLUX TRANSPORTERS ATP7A;
OXIDATIVE STRESS;
MITOCHONDRIAL-DNA;
DRUG-RESISTANCE;
GLUTATHIONE;
CARCINOMA;
MECHANISMS;
APOPTOSIS;
SYSTEM;
ROS;
D O I:
10.2217/nnm-2020-0400
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 ;
0836 ;
090102 ;
100705 ;
摘要:
Aim: To sensitize cisplatin (Cis)-resistant ovarian cancer cells toward Cis using Cis-loaded nanostructured lipid carriers (CisNLCs). Materials & methods: CisNLCs were synthesized and characterized using dynamic light scattering, Fourier transform IR and x-ray diffraction (XRD). Sensitivity of PA-1 and CaOV3 cells to Cis and its biotoxicity were assessed. Further, expression of the Cis-resistance markers GSTPi and ATP7B, and apoptotic markers Bax, Bcl2 and Cas9 were quantified by real-time PCR. Results: The size of synthesized CisNLCs was approximately 179.3 +/- 2.32 nm and surface charge was -33.9 +/- 1.47 mV. IC50 was 210 mu g/ml in PA-1 and 500 mu g/ml in CaOV3. CisNLCs modulated reactive oxygen species levels in CaOV3 cells. Reduced GSTPi and decreased Cis efflux via ATP7B sequestration caused Cis to accumulate in cytoplasm, thereby augmenting apoptosis in cells. Conclusion: CisNLCs sensitize CaOV3 by redox resetting, indicating their immense therapeutic potential.
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页码:979 / 995
页数:17
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