Cerium(IV) oxide:silver/graphene oxide (CeO2:Ag/GO) nanoparticles modulate gene expression and inhibit colorectal cancer cell growth: a pathway-centric therapeutic approach

Colorectal cancer (CRC) represents a substantial global health burden, necessitating advancements in diagnostic and therapeutic modalities. This study aimed to investigate the potential of CeO2/GO nanoparticles (NPs) in managing CRC and to compare their efficacy with Ag-doped CeO2 (CeO2:Ag) NPs. The synthesis of cerium oxide (CeO2) and graphene oxide (GO) was meticulously performed, followed by a comprehensive evaluation of NPs' toxicity and their impact on apoptosis-related genes in CRC cells. Characterization techniques, including XRD, EDX, SEM, TEM, FT-IR, and DLS, validated the successful synthesis and unique properties of CeO2:Ag/GO NPs. XRD confirmed the CeO2 and GO structures, while EDX analysis confirmed high purity in the synthesized NPs and uniform element distribution in CeO2/GO NPs. SEM and TEM micrographs illustrated CeO2 NPs attached to graphene sheets, showcasing reduced size post-attachment. FT-IR revealed characteristic peaks for CeO2 and GO, confirming their composite structure. DLS showed an average NP size of 20 nm in solution. Notably, MTT assays demonstrated that CeO2:Ag/GO NPs exhibited enhanced cytotoxicity against CRC cells (C-26 cell line) compared to CeO2:Ag NPs, with higher doses showing heightened efficacy. CeO2:Ag/GO NPs induced stronger growth inhibition and apoptosis in CRC cells, which was linked to their improved cellular uptake and ability to target multiple cancer-related pathways. In contrast, GO NPs alone lacked cytotoxic effects. Gene expression analysis via qPCR revealed CeO2:Ag/GO NPs significantly downregulated Zeb-1, VEGF, Cyclin-D1, and Twist compared to controls, altering cancer-related pathways more effectively than CeO2:Ag NPs. Additionally, CeO2:Ag/GO NPs significantly upregulated BAX and Caspase-1 while downregulating Bcl-2, implicating a more potent apoptotic response. This study highlights the advantage of CeO2:Ag/GO NPs over CeO2:Ag NPs in impeding CRC cell growth and inducing apoptosis, offering a promising foundation for innovative therapeutic strategies.

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Publication Details

Journal
Cancer Nanotechnology
Published
2024-12-01
DOI
https://doi.org/10.1186/s12645-024-00300-3
Primary Topic
Graphene and Nanomaterials Applications
Type
article
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article

Cerium(IV) oxide:silver/graphene oxide (CeO2:Ag/GO) nanoparticles modulate gene expression and inhibit colorectal cancer cell growth: a pathway-centric therapeutic approach

Omid Reza Tamtaji, Fatemeh Nabavizadeh, Majid Nejati, Mina Homayoonfal et al.
1 links
Cancer Nanotechnology
Graphene and Nanomaterials Applications
article

Cerium(IV) oxide:silver/graphene oxide (CeO2:Ag/GO) nanoparticles modulate gene expression and inhibit colorectal cancer cell growth: a pathway-centric therapeutic approach

Omid Reza Tamtaji, Fatemeh Nabavizadeh, Majid Nejati, Mina Homayoonfal, Amirreza Ostadian, Bahareh Mohammadzadeh, Hamed Mirzaei, Maryam Mahjoubin‐Tehran, Neda Rahimian, Merat Karimi, Elaheh Ghelichi
article en

Abstract

Colorectal cancer (CRC) represents a substantial global health burden, necessitating advancements in diagnostic and therapeutic modalities. This study aimed to investigate the potential of CeO2/GO nanoparticles (NPs) in managing CRC and to compare their efficacy with Ag-doped CeO2 (CeO2:Ag) NPs. The synthesis of cerium oxide (CeO2) and graphene oxide (GO) was meticulously performed, followed by a comprehensive evaluation of NPs' toxicity and their impact on apoptosis-related genes in CRC cells. Characterization techniques, including XRD, EDX, SEM, TEM, FT-IR, and DLS, validated the successful synthesis and unique properties of CeO2:Ag/GO NPs. XRD confirmed the CeO2 and GO structures, while EDX analysis confirmed high purity in the synthesized NPs and uniform element distribution in CeO2/GO NPs. SEM and TEM micrographs illustrated CeO2 NPs attached to graphene sheets, showcasing reduced size post-attachment. FT-IR revealed characteristic peaks for CeO2 and GO, confirming their composite structure. DLS showed an average NP size of 20 nm in solution. Notably, MTT assays demonstrated that CeO2:Ag/GO NPs exhibited enhanced cytotoxicity against CRC cells (C-26 cell line) compared to CeO2:Ag NPs, with higher doses showing heightened efficacy. CeO2:Ag/GO NPs induced stronger growth inhibition and apoptosis in CRC cells, which was linked to their improved cellular uptake and ability to target multiple cancer-related pathways. In contrast, GO NPs alone lacked cytotoxic effects. Gene expression analysis via qPCR revealed CeO2:Ag/GO NPs significantly downregulated Zeb-1, VEGF, Cyclin-D1, and Twist compared to controls, altering cancer-related pathways more effectively than CeO2:Ag NPs. Additionally, CeO2:Ag/GO NPs significantly upregulated BAX and Caspase-1 while downregulating Bcl-2, implicating a more potent apoptotic response. This study highlights the advantage of CeO2:Ag/GO NPs over CeO2:Ag NPs in impeding CRC cell growth and inducing apoptosis, offering a promising foundation for innovative therapeutic strategies.

Cancer NanotechnologyVol. 15(1)
University of Kashan (IR), Amirkabir University of Technology (IR), Iran University of Medical Sciences (IR), Mashhad University of Medical Sciences (IR), Kashan University of Medical Sciences (IR), Biotechnology Research Center (IR), Firoozgar General Hospital (IR), Tehran University of Medical Sciences (IR)
Good health and well-being
Openalex Percentile: Top 78%
Graphene and Nanomaterials Applications
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