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Copper/Tin Nanocomposites-Loaded Exosomes Induce Apoptosis and Cell Cycle Arrest at G0/G1 Phase in Skin Cancer Cell Line
被引:9
作者:
Abd-Rabou, Ahmed A.
[1
,2
]
Kishta, Mohamed S.
[1
,2
]
Yakout, Saad M.
[3
]
Youssef, Ahmed M.
[3
]
Abdallah, Ahmed N.
[1
,2
]
Ahmed, Hanaa H.
[1
,2
]
机构:
[1] Natl Res Ctr, Med Res & Clin Studies Inst, Hormones Dept, Cairo, Egypt
[2] Natl Res Ctr, Ctr Excellence Adv Sci, Stem Cell Lab, Cairo 12622, Egypt
[3] Natl Res Ctr, Inorgan Chem Ind & Mineral Resources Res Inst, Inorgan Chem Dept, Cairo, Egypt
关键词:
Exosomes;
CuS/SnS nanocomposites;
A431 skin cancer cell line;
Apoptosis;
Cell cycle;
OXIDE NANOPARTICLES;
BIOSYNTHESIS;
DELIVERY;
FUTURE;
GROWTH;
D O I:
10.1002/cbdv.202400486
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
This study aims to explore the efficacy of Copper/Tin (CuS/SnS) nanocomposites loaded into exosomes against skin cancer A431 cell line. CuS/SnS nanocomposites (S1, S2, S3) were synthesized and characterized, then loaded into exosomes (Exo) (S1-Exo, S2-Exo and S3-Exo) and characterized. After that, the loaded samples were investigated in vitro against A431 using cytotoxicity, apoptosis, and cell cycle assays. CuS/SnS nanocomposites were indexed to hexagonal CuS structure and orthorhombic alpha-SnS phase and showed nano-rode shape. The exosomes loaded with nanocomposites were regular and rounded within the size of 120 nm, with no signs of broken exosomes or leakage of their contents. The cytotoxicity assay indicated the enhanced cytotoxic of S1-Exo versus the free nano-form S1 on A431. Interestingly, S1-Exo recorded 1.109 times more than DOX in its anti-skin cancer capacity. Moreover, S1-Exo recorded 40.2 % for early apoptosis and 22.1 % for late apoptosis. Furthermore, it displayed impact in arresting the cancer cell cycle at G0/G1 phase and reducing G2/M phase. Noteworthy, loaded nanocomposites were safe against normal HSF skin cells. In conclusion, the loaded CuS/SnS nanocomposites into the exosomes could be of great potential as anti-skin cancer candidates through induction of apoptosis and promotion of the cell cycle arrest at G0/G1 phase. image
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页数:17
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