Autor: |
Abd-Rabou AA; Hormones Department, Medical Research Division, National Research Centre, P.O. 12622, Dokki, Giza, Egypt., Shalby AB; Hormones Department, Medical Research Division, National Research Centre, P.O. 12622, Dokki, Giza, Egypt., Ahmed HH; Hormones Department, Medical Research Division, National Research Centre, P.O. 12622, Dokki, Giza, Egypt. hanaaomr@yahoo.com. |
Jazyk: |
angličtina |
Zdroj: |
Biological trace element research [Biol Trace Elem Res] 2019 Jan; Vol. 187 (1), pp. 80-91. Date of Electronic Publication: 2018 May 11. |
DOI: |
10.1007/s12011-018-1360-8 |
Abstrakt: |
Drug resistance is a major challenge of breast and colon cancer therapies leading to treatment failure. The main objective of the current study is to investigate whether selenium nanoparticles (nano-Se) can induce the chemo-sensitivity of 5-fluorouracil (FU)-encapsulated poly (D, L-lactide-co-glycolide) nanoparticles (nano-FU) in breast and colon cancer cell lines. Nano-Se and nano-FU were synthesized and characterized, then applied individually or in combination upon MCF7, MDA-MB-231, HCT 116, and Caco-2 cancerous cell lines. Cytotoxicity, cellular glucose uptake, and apoptosis, as well as malondialdehyde (MDA), nitric oxide (NO), and zinc (Zn) levels, were investigated upon the different treatments. We have resulted that nano-FU induced cell death in MCF7 and Caco-2 more effectively than MDA-MB-231 and HCT 116 cell lines. Moreover, nano-FU plus nano-Se potentiate MCF7 and Caco-2 chemo-sensitivity were higher than MDA-MB-231 and HCT 116 cancerous cell lines. It is relevant to note that Se and FU nano-formulations inhibited cancer cell bioenergetics via glucose uptake slight blockage. Furthermore, nano-FU increased the levels of NO and MDA in media over cancer cells, while their combinations with nano-Se rebalance the redox status with Zn increment. We noticed that MCF7 cell line is sensitive, while MDA-MB-231 cell line is resistant to Se and nano-Se. This novel approach could be of great potential to enhance the chemo-sensitivity in breast and colon cancer cells. |
Databáze: |
MEDLINE |
Externí odkaz: |
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