Evidence map›Paper›PMID 41068915›Full record

ReviewMolecular cancer2025

Advances in RNA-based cancer therapeutics: pre-clinical and clinical implications.

Yubo Yan, Shuang Liu, Jie Wen, Yunlong He, Chenyang Duan, Noushin Nabavi, Milad Ashrafizadeh, Gautam Sethi, Lubin Liu, Rong Ma

Abstract readReview
In one paragraph

Review in Molecular cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

28 citing papers in PubMed.

  1. Article
  2. Review
  3. RNA splicing in health and disease.Molecular biomedicine · 2026
    Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Review
  14. Review
  15. Article
  16. Review
  17. Review
  18. Article
  19. RNA therapeutic targeting of recalcitrant and rare cancers.Exploration of targeted anti-tumor therapy · 2026
    Review
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Yubo Yan *Department of Thoracic Surgery, Harbin Medical University Cancer Hospital, Harbin, China.
Shuang Liu *Department of Gynecology, Harbin Medical University Cancer Hospital, 150 Haping RD, Harbin, Heilongjiang, China.
Jie Wen *Department of Interventional Oncology, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Yunlong HeDepartment of Radiation Oncology, Harbin Medical University Cancer Hospital, Harbin, Heilongjiang, China.
Chenyang DuanDepartment of Anesthesiology, The Second Affiliated Hospital of Chongqing Medical University, Chongqing, P.R. China.
Noushin NabaviIndependent Researcher, Victoria, BC, V8V 1P7, Canada.
Milad AshrafizadehDepartment of Radiation Oncology, Shandong Cancer Hospital and Institute, Shandong First Medical University, Shandong Academy of Medical Sciences, Jinan, 250000, Shandong, China.
Gautam SethiDepartment of Pharmacology and NUS Centre for Cancer Research, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, 117600, Singapore. phcgs@nus.edu.sg.
Lubin LiuDepartment of Obstetrics and Gynecology, Chongqing Health Center for Women and Children, No.64 Jintang Street, Chongqing, China. liulubin1975@126.com.
Rong MaDepartment of Gynecology, Harbin Medical University Cancer Hospital, 150 Haping RD, Harbin, Heilongjiang, China. 600543@hrbmu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer therapy has been revolutionised by the emergence of RNA-based therapeutics, providing several strategies and mechanisms to regulate gene expression via messenger RNA (mRNA), small interfering RNA (siRNA), microRNAs (miRNA), antisense oligonucleotides (ASOs), and RNA aptamers. The present review highlights the recent advances in the preclinical development and clinical applications of RNA-based therapeutics, focusing on the delivery strategies, biological targets, and pharmacological optimisation, together with key clinical data. mRNA therapeutics, especially those adapted from vaccine platforms are being developed for the cancer immunotherapy and protein replacement, while siRNAs and ASOs enable highly specific gene silencing and splice correction. miRNA therapies show potential for diverse oncogenic pathway control, despite ongoing challenges in the delivery and specificity. RNA aptamers are obtaining attention as tumor-targeting agents in the drug delivery systems. Progress in lipid nanoparticles, chemical modifications, and tissue-specific delivery has improved the stability and efficacy of these agents. Early-phase clinical trials report encouraging outcomes in both solid tumours and haematologic malignancies, particularly in overcoming resistance and modulating the tumor microenvironment (TME). Although challenges remain in scalability, immune activation, and deep-tumour penetration, RNA-based strategies are advancing towards integration into clinical oncology. Continued refinement of delivery technologies and targeted trial designs will be critical for translating these therapies into effective, personalized cancer treatments.

Indexed as

Genetic TherapyNeoplasmsRNAAnimalsAptamers, NucleotideClinical Trials as TopicDrug Delivery SystemsHumansMicroRNAsOligonucleotides, AntisenseRNA, MessengerRNA, Small InterferingAptamers, NucleotideMicroRNAsOligonucleotides, AntisenseRNARNA, MessengerRNA, Small InterferingAntisense oligonucleotidesCancer immunotherapyMRNA vaccineRNA aptamersSiRNA

Identifiers

PMID41068915
PMCPMC12512572

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.