The DOI matches its Crossref record; 203 of the 203 references it cites were found in a registry or an index.
mRNA-based cancer therapeutics
Abstract
Due to the fact that mRNA technology allows the production of diverse vaccines and treatments in a shorter time frame and with reduced expense compared to conventional approaches, there has been a surge in the use of mRNA-based therapeutics in recent years. With the aim of encoding tumour antigens for cancer vaccines, cytokines for immunotherapy, tumour suppressors to inhibit tumour development, chimeric antigen receptors for engineered T cell therapy or genome-editing proteins for gene therapy, many of these therapeutics have shown promising efficacy in preclinical studies, and some have even entered clinical trials. Given the evidence supporting the effectiveness and safety of clinically approved mRNA vaccines, coupled with growing interest in mRNA-based therapeutics, mRNA technology is poised to become one of the major pillars in cancer drug development. In this Review, we present in vitro transcribed mRNA-based therapeutics for cancer treatment, including the characteristics of the various types of synthetic mRNA, the packaging systems for efficient mRNA delivery, preclinical and clinical studies, current challenges and future prospects in the field. We anticipate the translation of promising mRNA-based treatments into clinical applications, to ultimately benefit patients.
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“It is possible to have adverse effects and safety concerns associated with the expression of proteins in non-target cells or tissues [53].”
From Exosome for mRNA delivery: Strategies and therapeutic applications (2024) · cites this paper as [53]
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Items 201–203 of 203
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Treatment success in hereditary transthyretin amyloidosis
Fyfe, I. (2018) · Nature Reviews Neurology · doi:10.1038/s41582-018-0048-1 · Cited by 7
Startups set off new wave of mRNA therapeutics
Dolgin, E. (2021) · Nature Biotechnology · doi:10.1038/s41587-021-01056-6 · Cited by 7
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- Chew, W. L. Immunity to CRISPR Cas9 and Cas12a therapeutics. Wiley Interdiscip. Rev. Syst. Biol. Med. 10, e1408 (2018).
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Adjuvant and neoadjuvant immunotherapies in hepatocellular carcinoma
Llovet, J. M., Pinyol, R., Yarchoan, M., Singal, A. G., Marron, T. U., Schwartz, M., Pikarsky, E., Kudo, M., & Finn, R. S. (2024) · Nature Reviews Clinical Oncology · doi:10.1038/s41571-024-00868-0 · Cited by 391
Exosome for mRNA delivery: Strategies and therapeutic applications
Iqbal, Z., Rehman, K., Mahmood, A., Shabbir, M., Liang, Y., Duan, L., & Zeng, H. (2024) · Journal of Nanobiotechnology · doi:10.1186/s12951-024-02634-x · Cited by 144
Han, E. L., Padilla, M. S., Palanki, R., Kim, D., Mrksich, K., Li, J. J., Tang, S., Yoon, I.-C., & Mitchell, M. J. (2024) · Nano Letters · doi:10.1021/acs.nanolett.3c03509 · Cited by 72
Metadata
- Authors
- Liu, C., Shi, Q., Huang, X., Koo, S., Kong, N., & Tao, W.
- Affiliations
- Brigham and Women's Hospital (US)
- Corresponding author
- Kong, Na
- Tao, Wei
- Venue
- Nature Reviews Cancer
- Published
- 2023-06-13
- Volume
- 23
- Issue
- 8
- Pages
- 526-543
- ISSN
- 1474-175X (ISSN-L)
- 1474-1768
- OpenAlex
- W4380568974
- Semantic Scholar
- 51029cd9a0af75f7f0de6dc2c45583bba600345a
- Cited by
- 500
- References
- 203
- Citations by year
- 2026: 137 · 2025: 190 · 2024: 138 · 2023: 35
- FWCI
- 13.18
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- Locations
- Nature reviews. Cancer (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Interference and Gene Delivery
- Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biotechnology › Bacterial Cancer Therapy
- Keywords
- mRNA therapeutics, cancer vaccines, mRNA vaccines, mRNA delivery, in vitro transcribed mRNA, synthetic mRNA, tumor antigens, cytokines, tumour suppressor, CAR T-cell therapy, genome editing, gene therapy, cancer immunotherapy, personalized medicine, clinical trials
- MeSH terms
- Receptors, Chimeric Antigen, Humans, Immunotherapy, Neoplasms, RNA, Messenger, Cytokines
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