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Gold Nanoparticles and Graphene Oxide Flakes Enhance Cancer Cells' Phagocytosis through Granzyme-Perforin-Dependent Biomechanism.
Al-Omar, Mohsen S; Jabir, Majid; Karsh, Esraa; Kadhim, Rua; Sulaiman, Ghassan M; Taqi, Zainab J; Khashan, Khawla S; Mohammed, Hamdoon A; Khan, Riaz A; Mohammed, Salman A A.
Affiliation
  • Al-Omar MS; Department of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, Qassim University, Qassim 51452, Saudi Arabia.
  • Jabir M; Medicinal Chemistry and Pharmacognosy Department, Faculty of Pharmacy, Jordan University of Science and Technology, Irbid 22110, Jordan.
  • Karsh E; Department of Applied Sciences, University of Technology, Baghdad 10066, Iraq.
  • Kadhim R; Department of Applied Sciences, University of Technology, Baghdad 10066, Iraq.
  • Sulaiman GM; Department of Applied Sciences, University of Technology, Baghdad 10066, Iraq.
  • Taqi ZJ; Department of Applied Sciences, University of Technology, Baghdad 10066, Iraq.
  • Khashan KS; Department of Applied Sciences, University of Technology, Baghdad 10066, Iraq.
  • Mohammed HA; Department of Applied Sciences, University of Technology, Baghdad 10066, Iraq.
  • Khan RA; Department of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, Qassim University, Qassim 51452, Saudi Arabia.
  • Mohammed SAA; Department of Pharmacognosy, Faculty of Pharmacy, Al-Azhar University, Cairo 11371, Egypt.
Nanomaterials (Basel) ; 11(6)2021 May 24.
Article in En | MEDLINE | ID: mdl-34073808
ABSTRACT
The study aimed to investigate the roles of gold nanoparticles (GNPs) and graphene oxide flakes (GOFs) as phagocytosis enhancers against cancer cells. The nanomaterials were characterized through SEM and UV-VIS absorptions. The GNPs and GOFs increased the macrophages' phagocytosis ability in engulfing, thereby annihilating the cancer cells in both in vitro and in vivo conditions. The GNPs and GOFs augmented serine protease class apoptotic protein, granzyme, passing through the aquaporin class protein, perforin, with mediated delivery through the cell membrane site for the programmed, calibrated, and conditioned cancer cells killing. Additionally, protease inhibitor 3,4-dichloroisocoumarin (DCI) significantly reduced granzyme and perforin activities of macrophages. The results demonstrated that the GOFs and GNPs increased the activation of phagocytic cells as a promising strategy for controlling cancer cells by augmenting the cell mortality through the granzyme-perforin-dependent mechanism.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Nanomaterials (Basel) Year: 2021 Document type: Article Affiliation country: Saudi Arabia Publication country: CH / SUIZA / SUÍÇA / SWITZERLAND

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Nanomaterials (Basel) Year: 2021 Document type: Article Affiliation country: Saudi Arabia Publication country: CH / SUIZA / SUÍÇA / SWITZERLAND