The DOI matches its Crossref record; 177 of the 179 references it cites were found in a registry or an index.
An RNA toolbox for cancer immunotherapy
Abstract
Cancer immunotherapy has revolutionized oncology practice. However, current protein and cell therapy tools used in cancer immunotherapy are far from perfect, and there is room for improvement regarding their efficacy and safety. RNA-based structures have diverse functions, ranging from gene expression and gene regulation to pro-inflammatory effects and the ability to specifically bind different molecules. These functions make them versatile tools that may advance cancer vaccines and immunomodulation, surpassing existing approaches. These technologies should not be considered as competitors of current immunotherapies but as partners in synergistic combinations and as a clear opportunity to reach more efficient and personalized results. RNA and RNA derivatives can be exploited therapeutically as a platform to encode protein sequences, provide innate pro-inflammatory signals to the immune system (such as those denoting viral infection), control the expression of other RNAs (including key immunosuppressive factors) post-transcriptionally and conform structural scaffoldings binding proteins that control immune cells by modifying their function. Nascent RNA immunotherapeutics include RNA vaccines encoding cancer neoantigens, mRNAs encoding immunomodulatory factors, viral RNA analogues, interference RNAs and protein-binding RNA aptamers. These approaches are already in early clinical development with promising safety and efficacy results.
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“RNA vaccines, for example, have exhibited encouraging results in both infection therapy and cancer immunotherapy.[6, 7, 11–15]”
From RNA delivery biomaterials for the treatment of genetic and rare diseases (2019) · cites this paper as [7]
Citations
Cites
Improved Survival with Ipilimumab in Patients with Metastatic Melanoma
Hodi, F. S., O'Day, S. J., McDermott, D. F., Weber, R. W., Sosman, J. A., Haanen, J. B., Gonzalez, R., Robert, C., Schadendorf, D., Hassel, J. C., et al. (2010) · New England Journal of Medicine · doi:10.1056/nejmoa1003466 · Cited by 15,155
Tuerk, C., & Gold, L. (1990) · Science · doi:10.1126/science.2200121 · Cited by 10,421
In vitro selection of RNA molecules that bind specific ligands
Ellington, A. D., & Szostak, J. W. (1990) · Nature · doi:10.1038/346818a0 · Cited by 9,845
Pattern Recognition Receptors and Inflammation
Takeuchi, O., & Akira, S. (2010) · Cell · doi:10.1016/j.cell.2010.01.022 · Cited by 8,895
Origins and Mechanisms of miRNAs and siRNAs
Carthew, R. W., & Sontheimer, E. J. (2009) · Cell · doi:10.1016/j.cell.2009.01.035 · Cited by 5,161
mRNA vaccines — a new era in vaccinology
Pardi, N., Hogan, M. J., Porter, F. W., & Weissman, D. (2018) · Nature Reviews Drug Discovery · doi:10.1038/nrd.2017.243 · Cited by 4,667
N6-methyladenosine-dependent regulation of messenger RNA stability
Wang, X., Lu, Z., Gomez, A., Hon, G. C., Yue, Y., Han, D., Fu, Y., Parisien, M., Dai, Q., Jia, G., et al. (2014) · Nature · doi:10.1038/nature12730 · Cited by 4,558
Pan, Q., Shai, O., Lee, L. J., Frey, B. J., & Blencowe, B. J. (2008) · Nature Genetics · doi:10.1038/ng.259 · Cited by 3,951
Unique features of long non-coding RNA biogenesis and function
Quinn, J. J., & Chang, H. Y. (2015) · Nature Reviews Genetics · doi:10.1038/nrg.2015.10 · Cited by 3,700
Chimeric Antigen Receptor–Modified T Cells for Acute Lymphoid Leukemia
Grupp, S. A., Kalos, M., Barrett, D., Aplenc, R., Porter, D. L., Rheingold, S. R., Teachey, D. T., Chew, A., Hauck, B., Wright, J. F., et al. (2013) · New England Journal of Medicine · doi:10.1056/nejmoa1215134 · Cited by 3,509
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Items 201–230 of 230
RNA with chemotherapeutic base analogues as a dual-functional anti-cancer drug
Jarzębska, N. T., Tusup, M., Frei, J., Weiß, T., Holzinger, T., Mellett, M., Diken, M., Bredl, S., Weller, M., Speck, R. F., et al. (2022) · OncoImmunology · doi:10.1080/2162402x.2022.2147665 · Cited by 1
“aptamers), or express proteins of interest (antigens in vaccines or therapeutic proteins such as cytokines).(1) RNA is also a natural danger signal recognized by several immune receptors and activating a broad range of cells including Dendritic cells (DCs), plasmacytoid DCs (pDCs), B cells, monocytes and Natural Kille…”
BackgroundCancer Nanoimmunotherapy: Recent Advances and New Opportunities
Veluchamy, C., Kamaraj, S., Ramasamy, T., Sánchez‐Cárdenas, M., & Sánchez‐Olmos, L. A. (2021) · Nanotechnology in the life sciences · doi:10.1007/978-3-030-76263-6_6 · Cited by 1
Fluorescent Aptamers for Detection and Treatment of Pathogenic Bacteria and CancerPreprint
Sharma, A., & Ramena, G. T. (2021) · Preprints.org · doi:10.20944/preprints202101.0471.v1 · Cited by 1
A novel Adenoviral miRNA, a candidate for development of a novel gene therapy startegy
Danish, B. (2019) · Uppsala University Publications (Uppsala University)
Conforti, A., Palombo, F., & Aurisicchio, L. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-823901-8.00002-9
In silico antibody-peptide epitope prediction for personalized cancer therapy
Jacobs, I., Ming, L. C., Mong, J. C. Y., Μaragoudakis, M., & Malik, N. (2023) · Frontiers in Applied Mathematics and Statistics · doi:10.3389/fams.2023.1150381
“, map the qualitative measures “positive,” “positivehigh,” and “negative” to bins of intervals [30, 300), [300, 1, 500), [0,−1500) where the qualitative measures class is assigned to all measurements whose PMBC values fall into its respective bin range.”
BackgroundIn Vitro Evolution and Aptamers
de Franciscis, V., Mayer, G., & Giangrande, P. H. (2022) · Royal Society of Chemistry eBooks · doi:10.1039/9781837671328-00403
Di-Trani, C. A. (. A. (2023) · Deposito Adademico Digital Universidad De Navarra (University of Navarra) · doi:10.15581/10171/67876
Nguyen, D. H., Uddin, M. J., Al‐Tawfiq, J. A., Memish, Z. A., & Chu, D. (2024) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2023.12.004
mRNA Vaccination for Breast Cancer
Schmidt, M., & Sahin, U. (2024) · Cancer immunotherapy · doi:10.1007/13905_2024_46
An Update on Recent Treatment Approaches for Prostate Cancer
Bijanvand, A., Khalilian, S., Loghman, A. H., & Rezaei, N. (2024) · Springer eBooks · doi:10.1007/978-3-030-80962-1_393-1
Immunotherapy for Prostate Cancer
Bijanvand, A., Khalilian, S., Loghman, A. H., & Rezaei, N. (2024) · Springer eBooks · doi:10.1007/978-3-030-80962-1_393-2
Tungariya, G. (2025) · International Journal for Research in Applied Science and Engineering Technology · doi:10.22214/ijraset.2025.69295
Lipid Based Nano Carriers in Cancer Therapy
Nerkar, K. B. (2025) · International Journal for Research in Applied Science and Engineering Technology · doi:10.22214/ijraset.2025.69259
Arrizabalaga, L., Melero, I., Berraondo, P., & Aranda, F. (2025) · OncoImmunology · doi:10.1080/2162402x.2025.2510998
“8,9 Although our findings have been demonstrated with TransIT®, which is not approved for clinical use, they provide a compelling proof-of-concept.”
Shankar, D., Mishra, D. K., Singh, A., Pathak, N., Minocha, N., Pandey, P., & Malhotra, P. (2025) · Current Nanomedicine · doi:10.2174/0124681873339647250214070805
The RNA-based immunotherapy and future perspectives
Atalay, B. R., Aydemir, E., & Ayaz, F. (2025) · Discover Immunity. · doi:10.1007/s44368-025-00012-9
“As a result, more than 20 mRNA-based cancer immunotherapies have progressed into clinical trials, showing encouraging outcomes [27, 101, 102].”
Immunotherapy for Prostate Cancer
Bijanvand, A., Khalilian, S., Loghman, A. H., & Rezaei, N. (2025) · Springer eBooks · doi:10.1007/978-3-032-00769-8_393
Beyond mutations: personalising oncology via RNA-editing
Fierro-Monti, I. (2026) · Frontiers in RNA Research · doi:10.3389/frnar.2026.1779364
Cancer immunotherapy : efficacy and safety of a melanin-based vaccine
Cuzzubbo, S. (2021) · theses.fr (ABES) · doi:10.70675/2e1d38a6z8d99z458dza769zb7bccda2b709
Engineering polymeric RNA scaffolds as programmable combinatorial innate immune agonists
Yang, Y. Z., Alvarez, A. K., Wang, W., Issa, E. C., Dorsey, E., & Wu, C. (2026) · Nucleic Acids Research · doi:10.1093/nar/gkag328
“Comparison of TLR7 activation levels showed that polyR-NAs containing GU-rich ssRNA regions activated TLR7 more strongly, consistent with previous observations [ 29 ].”
Wang, S., Zhang, J., Zheng, M., Feng, Y., & Li, T. (2026) · Frontiers in Oncology · doi:10.3389/fonc.2026.1802679
Mustafa, A., Irfan, T., Babar, M. M., & Rajadas, J. (2026) · Springer eBooks · doi:10.1007/978-981-95-3957-4_24
Advances in RNA-Based Therapeutics in Oncology
Lopes-Cardoso, H., Panão-Costa, J., Amaral, A. T., Soares-Gonçalves, J., Neves, B. F., Voronovska, A., Batista, A., Biscaia-Caleiras, M., Fonseca, N. A., Simões, S., et al. (2026) · Springer handbooks · doi:10.1007/978-3-032-01636-2_19
Gantai, Y., Yang, Z., Chen, Y., Chen, M., Hu, Y. M., Ye, T., Xu, J., Zhou, S., Yu, Y., Chen, Y., et al. (2026) · Pharmaceutics · doi:10.3390/pharmaceutics18060660
Spatial Tail Design in Ionizable Lipids Enhances the Safety and Efficacy of mRNA Delivery
Li, H., Tian, C., Kong, W., Weiss, J., Gang, J., Zhong, T., Ma, Y., Xu, J., Tai, W., Zeng, F., et al. (2026) · Small Methods · doi:10.1002/smtd.70796
Lipoplex Nanoparticle-Based RNA Delivery to 3D Melanoma Spheroids
Rudolf, R., Cesetti, T., Keller, F., & Hafner, M. (2026) · Methods in molecular biology · doi:10.1007/978-1-0716-5619-8_37
Metadata
- Authors
- Pastor, F., Berraondo, P., Etxeberria, I., Frederick, J., Sahin, U., Gilboa, E., & Melero, I.
- Affiliations
- Centro de Investigación Médica Aplicada (ES)
- Navarre Institute of Health Research (ES)
- Moderna Therapeutics (United States) (US)
- University of Miami (US)
- Corresponding author
- Melero, Ignacio
- Venue
- Nature Reviews Drug Discovery
- Published
- 2018-09-07
- Volume
- 17
- Issue
- 10
- Pages
- 751-767
- ISSN
- 1474-1776 (ISSN-L)
- 1474-1784
- OpenAlex
- W2889813782
- Cited by
- 229
- References
- 179
- Citations by year
- 2026: 11 · 2025: 27 · 2024: 24 · 2023: 39 · 2022: 40 · 2021: 33 · 2020: 27 · 2019: 27 · 2018: 1
- FWCI
- 2.25
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Reviews Drug Discovery (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
- Health Sciences › Medicine › Oncology › Cancer Immunotherapy and Biomarkers
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Interference and Gene Delivery
- Keywords
- cancer immunotherapy, RNA vaccines, neoantigens, mRNA vaccines, RNA interference, RNA aptamers, immunomodulation, innate immune activation, post-transcriptional regulation, cancer vaccines, combination immunotherapy
- MeSH terms
- Animals, Humans, Immunotherapy, Neoplasms, RNA, Cancer Vaccines, RNA Interference, Immunomodulation
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