Effective delivery of anti-PD-L1 siRNA with human heavy chain ferritin (HFn) in acute myeloid leukemia cell lines.


Journal

Medical oncology (Northwood, London, England)
ISSN: 1559-131X
Titre abrégé: Med Oncol
Pays: United States
ID NLM: 9435512

Informations de publication

Date de publication:
13 May 2024
Historique:
received: 20 03 2024
accepted: 24 04 2024
medline: 13 5 2024
pubmed: 13 5 2024
entrez: 13 5 2024
Statut: epublish

Résumé

Because of the high biocompatibility, self-assembly capability, and CD71-mediated endocytosis, using human heavy chain ferritin (HFn) as a nanocarrier would greatly increase therapeutic effectiveness and reduce possible adverse events. Anti-PD-L1 siRNA can downregulate the level of PD-L1 on tumor cells, resulting in the activation of effector T cells against leukemia. Therefore, this study aimed to produce the tumor-targeting siPD-L1/HFn nanocarrier. Briefly, the HFn coding sequence was cloned into a pET-28a, and the constructed expression plasmid was subsequently transformed into E. coli BL21. After induction of Isopropyl β-D-1-thiogalactopyranoside (IPTG), HFn was purified with Ni-affinity chromatography and dialyzed against PBS. The protein characteristics were analyzed using SDS-PAGE, Western Blot, and Dynamic light scattering (DLS). The final concentration was assessed using the Bicinchoninic acid (BCA) assay. The encapsulation was performed using the standard pH system. The treatment effects of siPD-L1/HFn were carried out on HL-60 and K-562 cancer cell lines. The RT-PCR was used to determine the mRNA expression of PD-L1. The biocompatibility and excretion of siPD-L1/HFn have also been evaluated. The expression and purity of HFn were well verified through SDS-PAGE, WB, and DLS. RT-PCR analyses also showed significant siRNA-mediated PD-L1 silencing in both HL-60 and K-562 cells. Our study suggested a promising approach for siRNA delivery. This efficient delivery system can pave the way for the co-delivery of siRNAs and multiple chemotherapies to address the emerging needs of cancer combination therapy.

Identifiants

pubmed: 38739199
doi: 10.1007/s12032-024-02393-7
pii: 10.1007/s12032-024-02393-7
doi:

Substances chimiques

RNA, Small Interfering 0
B7-H1 Antigen 0
Apoferritins 9013-31-4
CD274 protein, human 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

149

Subventions

Organisme : Mazandran University of Medical Science
ID : 10600
Organisme : Mazandran University of Medical Science
ID : 10600

Informations de copyright

© 2024. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

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Auteurs

Misagh Rajabinejad (M)

Department of Immunology, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.

Reza Valadan (R)

Department of Immunology, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.
Molecular and Cell-Biology Research Center, Mazandaran University of Medical Sciences, Sari, Iran.

Mohsen Tehrani (M)

Department of Immunology, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.
Molecular and Cell-Biology Research Center, Mazandaran University of Medical Sciences, Sari, Iran.

Ahmad Najafi (A)

Department of Immunology, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.

Reza Negarandeh (R)

Department of Pharmaceutics, Faculty of Pharmacy, Mazandaran University of Medical Sciences, Sari, Iran.
Student Research Committee, Department of Pharmaceutics, Faculty of Pharmacy, Mazandaran University of Medical Sciences, Sari, Iran.

Majid Saeedi (M)

Department of Pharmaceutics, Faculty of Pharmacy, Mazandaran University of Medical Sciences, Sari, Iran.

Hossein Asgarian-Omran (H)

Department of Immunology, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran. Asgarianhossein@yahoo.com.
Gastrointestinal Cancer Research Center, Non-Communicable Diseases Institute, Mazandaran University of Medical Sciences, Sari, Iran. Asgarianhossein@yahoo.com.

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