Production of novel theranostic nano-vector based on superparamagnetic iron oxide nanoparticles/miR-497 targeting colorectal cancer

Abstract Colorectal cancer (CRC) is a serious public health concern worldwide. Immune checkpoint inhibition medication is likely to remain a crucial part of CRC clinical management. This study aims to create new super paramagnetic iron oxide nano-carrier (SPION) that can effectively transport miRNA...

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Main Authors: Asmaa M. Elfiky, May M. Eid, May El-Manawaty, Zeinab A. Elshahid, Elham Mohamed Youssef, Khaled Mahmoud
Format: Article
Language:English
Published: Nature Portfolio 2025-02-01
Series:Scientific Reports
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Online Access:https://doi.org/10.1038/s41598-025-88165-3
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author Asmaa M. Elfiky
May M. Eid
May El-Manawaty
Zeinab A. Elshahid
Elham Mohamed Youssef
Khaled Mahmoud
author_facet Asmaa M. Elfiky
May M. Eid
May El-Manawaty
Zeinab A. Elshahid
Elham Mohamed Youssef
Khaled Mahmoud
author_sort Asmaa M. Elfiky
collection DOAJ
description Abstract Colorectal cancer (CRC) is a serious public health concern worldwide. Immune checkpoint inhibition medication is likely to remain a crucial part of CRC clinical management. This study aims to create new super paramagnetic iron oxide nano-carrier (SPION) that can effectively transport miRNA to specific CRC cell lines. In addition, evaluate the efficiency of this nano-formulation as a therapeutic candidate for CRC. Bioinformatics tools were used to select a promising tumor suppressor miRNA (mir-497-5p). Green route, using Fusarium oxyporium fungal species, manipulated for the synthesis of SPION@Ag@Cs nanocomposite as a carrier of miR-497-5p. That specifically targets the suppression of PD1/PDL1 and CTLA4pathways for colorectal therapy. UV/visible and FTIR spectroscopy, Zeta potential and MTT were used to confirm the allocation of the miR-497 on SPION@Ag@Cs and its cytotoxicity against CRC cell lines. Immunofluorescence was employed to confirm transfection of cells with miR-497@NPs, and the down- regulation of CTLA4 in HT29, and Caco2 cell lines. On the other hand, PDL1 showed a significant increase in colorectal cell lines (HT-29 and Caco-2) in response to mir497-5p@Nano treatment. The data suggest that the mir-497 -loaded SPION@Ag@Cs nano-formulation could be a good candidate for the suppression of CTLA4in CRC human cell lines. Consequently, the targeting miR-497/CTLA4 axis is a potential immunotherapy treatment strategy for CRC.
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spelling doaj-art-7c4fe1557c9949d89b7b969bff317ffb2025-02-09T12:33:42ZengNature PortfolioScientific Reports2045-23222025-02-0115111310.1038/s41598-025-88165-3Production of novel theranostic nano-vector based on superparamagnetic iron oxide nanoparticles/miR-497 targeting colorectal cancerAsmaa M. Elfiky0May M. Eid1May El-Manawaty2Zeinab A. Elshahid3Elham Mohamed Youssef4Khaled Mahmoud5Environmental and Occupational Medicine Department, Environment and Climate Change Research Institute, National Research CentrePhysics Institute, National Research CenterPharmaceutical Sciences Institute, Department of Pharmacognosy, National Research CentreChemistry of Natural and Microbial Products, Pharmaceutical Industry Research Institute, National Research CentreBiochemistry Department, National Research CentrePharmaceutical Sciences Institute, Department of Pharmacognosy, National Research CentreAbstract Colorectal cancer (CRC) is a serious public health concern worldwide. Immune checkpoint inhibition medication is likely to remain a crucial part of CRC clinical management. This study aims to create new super paramagnetic iron oxide nano-carrier (SPION) that can effectively transport miRNA to specific CRC cell lines. In addition, evaluate the efficiency of this nano-formulation as a therapeutic candidate for CRC. Bioinformatics tools were used to select a promising tumor suppressor miRNA (mir-497-5p). Green route, using Fusarium oxyporium fungal species, manipulated for the synthesis of SPION@Ag@Cs nanocomposite as a carrier of miR-497-5p. That specifically targets the suppression of PD1/PDL1 and CTLA4pathways for colorectal therapy. UV/visible and FTIR spectroscopy, Zeta potential and MTT were used to confirm the allocation of the miR-497 on SPION@Ag@Cs and its cytotoxicity against CRC cell lines. Immunofluorescence was employed to confirm transfection of cells with miR-497@NPs, and the down- regulation of CTLA4 in HT29, and Caco2 cell lines. On the other hand, PDL1 showed a significant increase in colorectal cell lines (HT-29 and Caco-2) in response to mir497-5p@Nano treatment. The data suggest that the mir-497 -loaded SPION@Ag@Cs nano-formulation could be a good candidate for the suppression of CTLA4in CRC human cell lines. Consequently, the targeting miR-497/CTLA4 axis is a potential immunotherapy treatment strategy for CRC.https://doi.org/10.1038/s41598-025-88165-3Colorectal cancerSPION@Ag@Cs nano-carriermiR-497-5pPD1/PDL1CTLA-4 oncogenes
spellingShingle Asmaa M. Elfiky
May M. Eid
May El-Manawaty
Zeinab A. Elshahid
Elham Mohamed Youssef
Khaled Mahmoud
Production of novel theranostic nano-vector based on superparamagnetic iron oxide nanoparticles/miR-497 targeting colorectal cancer
Scientific Reports
Colorectal cancer
SPION@Ag@Cs nano-carrier
miR-497-5p
PD1/PDL1
CTLA-4 oncogenes
title Production of novel theranostic nano-vector based on superparamagnetic iron oxide nanoparticles/miR-497 targeting colorectal cancer
title_full Production of novel theranostic nano-vector based on superparamagnetic iron oxide nanoparticles/miR-497 targeting colorectal cancer
title_fullStr Production of novel theranostic nano-vector based on superparamagnetic iron oxide nanoparticles/miR-497 targeting colorectal cancer
title_full_unstemmed Production of novel theranostic nano-vector based on superparamagnetic iron oxide nanoparticles/miR-497 targeting colorectal cancer
title_short Production of novel theranostic nano-vector based on superparamagnetic iron oxide nanoparticles/miR-497 targeting colorectal cancer
title_sort production of novel theranostic nano vector based on superparamagnetic iron oxide nanoparticles mir 497 targeting colorectal cancer
topic Colorectal cancer
SPION@Ag@Cs nano-carrier
miR-497-5p
PD1/PDL1
CTLA-4 oncogenes
url https://doi.org/10.1038/s41598-025-88165-3
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