» Articles » PMID: 39217377

MRNA Vaccines in Tumor Targeted Therapy: Mechanism, Clinical Application, and Development Trends

Overview
Journal Biomark Res
Publisher Biomed Central
Date 2024 Aug 31
PMID 39217377
Authors
Affiliations
Soon will be listed here.
Abstract

Malignant tumors remain a primary cause of human mortality. Among the various treatment modalities for neoplasms, tumor vaccines have consistently shown efficacy and promising potential. These vaccines offer advantages such as specificity, safety, and tolerability, with mRNA vaccines representing promising platforms. By introducing exogenous mRNAs encoding antigens into somatic cells and subsequently synthesizing antigens through gene expression systems, mRNA vaccines can effectively induce immune responses. Katalin Karikó and Drew Weissman were awarded the 2023 Nobel Prize in Physiology or Medicine for their great contributions to mRNA vaccine research. Compared with traditional tumor vaccines, mRNA vaccines have several advantages, including rapid preparation, reduced contamination, nonintegrability, and high biodegradability. Tumor-targeted therapy is an innovative treatment modality that enables precise targeting of tumor cells, minimizes damage to normal tissues, is safe at high doses, and demonstrates great efficacy. Currently, targeted therapy has become an important treatment option for malignant tumors. The application of mRNA vaccines in tumor-targeted therapy is expanding, with numerous clinical trials underway. We systematically outline the targeted delivery mechanism of mRNA vaccines and the mechanism by which mRNA vaccines induce anti-tumor immune responses, describe the current research and clinical applications of mRNA vaccines in tumor-targeted therapy, and forecast the future development trends of mRNA vaccine application in tumor-targeted therapy.

Citing Articles

Regulating Immune Responses Induced by PEGylated Messenger RNA-Lipid Nanoparticle Vaccine.

Jo H, Jeoung J, Kim W, Jeoung D Vaccines (Basel). 2025; 13(1).

PMID: 39852793 PMC: 11768904. DOI: 10.3390/vaccines13010014.


Vaccine Therapies for Prostate Cancer: Current Status and Future Outlook.

Zhou W, Lu X, Tian F, Luo Q, Zhou W, Yang S Vaccines (Basel). 2025; 12(12.

PMID: 39772046 PMC: 11679746. DOI: 10.3390/vaccines12121384.


The Utilization of PRAME in the Diagnosis, Prognosis, and Treatment of Melanoma.

Blount S, Liu X, McBride J Cells. 2024; 13(20.

PMID: 39451258 PMC: 11505691. DOI: 10.3390/cells13201740.

References
1.
Sahin U, Oehm P, Derhovanessian E, Jabulowsky R, Vormehr M, Gold M . An RNA vaccine drives immunity in checkpoint-inhibitor-treated melanoma. Nature. 2020; 585(7823):107-112. DOI: 10.1038/s41586-020-2537-9. View

2.
Nair S, Morse M, Boczkowski D, Cumming R, Vasovic L, Gilboa E . Induction of tumor-specific cytotoxic T lymphocytes in cancer patients by autologous tumor RNA-transfected dendritic cells. Ann Surg. 2002; 235(4):540-9. PMC: 1422470. DOI: 10.1097/00000658-200204000-00013. View

3.
Lezcano C, Jungbluth A, Busam K . PRAME Immunohistochemistry as an Ancillary Test for the Assessment of Melanocytic Lesions. Surg Pathol Clin. 2021; 14(2):165-175. PMC: 8152939. DOI: 10.1016/j.path.2021.01.001. View

4.
Kariko K, Buckstein M, Ni H, Weissman D . Suppression of RNA recognition by Toll-like receptors: the impact of nucleoside modification and the evolutionary origin of RNA. Immunity. 2005; 23(2):165-75. DOI: 10.1016/j.immuni.2005.06.008. View

5.
Khan M, Filipczak N, Torchilin V . Cell penetrating peptides: A versatile vector for co-delivery of drug and genes in cancer. J Control Release. 2020; 330:1220-1228. DOI: 10.1016/j.jconrel.2020.11.028. View