Evidence map›Paper›PMID 42176156›Full record

ReviewDiscover oncology2026

Exosome-mediated post-transcriptional oncogene regulation as a novel cancer therapeutic strategy.

Bunty Sharma, Kawaljit Singh Kaura, Ranjay Kumar Choudhary, Suresh Babu Kondaveeti, Malathi Hanumanthayya, Abhishek Chauhan, Sanjana Gupta, Himanshu Sharma, Anuj Ranjan, Ambrish Mishra and 1 more

Abstract readReview
In one paragraph

Review in Discover oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Bunty Sharma *Department of Biochemistry, All India Institute of Medical Sciences, Bathinda, 151001, India.
Kawaljit Singh Kaura *Department of Urology, All India Institute of Medical Sciences, Bathinda, 151001, India.
Ranjay Kumar ChoudharyCollege of Applied and Health Sciences, A'Sharqiyah University, P.O. Box 42, 400, Ibra, Sultanate of Oman.
Suresh Babu KondaveetiDepartment of Biochemistry, Symbiosis Medical College for Women, Symbiosis International (Deemed University), Pune, India.
Malathi HanumanthayyaDepartment of Biotechnology and Genetics, School of Sciences, JAIN (Deemed to be University), Bangalore, Karnataka, India.
Abhishek ChauhanAmity Institute of Environmental Toxicology, Safety and Management, Amity University, Noida, Uttar Pradesh, India.
Sanjana GuptaDepartment of Biotechnology, Himachal Pradesh University, Shimla, Himachal Pradesh, India.
Himanshu SharmaDepartment of Biochemistry, All India Institute of Medical Sciences, Bathinda, 151001, India.
Anuj RanjanAmity Institute of Environmental Toxicology, Safety and Management, Amity University, Noida, Uttar Pradesh, India.
Ambrish MishraDepartment of Human Genetics and Molecular Medicine, Central University of Punjab, Bhatinda, 151001, India.
Ujjawal SharmaDepartment of Human Genetics and Molecular Medicine, Central University of Punjab, Bhatinda, 151001, India. ujjawal.sharma@cup.edu.in.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Exosomes are tiny vesicles (30-150 nm in size) secreted by nearly every cell type that have lately emerged as essential regulators of intercellular communication and gene expression in cancer. They accommodate bioactive cargos such as miRNAs, lncRNAs, circRNAs, and mRNAs, all of which direct oncogene expression at the post-transcriptional level. Exosomal RNAs influence post-transcriptional and epigenetic regulatory mechanisms implicated in tumor activity, including mRNA degradation, translation repression and activation, alternative splicing interference, and epigenetic remodeling, which contribute to tumorigenic processes such as proliferation, angiogenesis, metastasis, immune evasion, and drug resistance. Tumor-derived exosomes also regulate the key oncogenic pathways such as PI3K/AKT, JAK/STAT, and Wnt/β-catenin to promote tumor stroma remodeling, thereby inducing macrophage M2 polarization, fibroblast transformation into cancer-associated fibroblasts, and pre-metastatic niche formation, favoring metastases. Targeting exosome-mediated oncogenic communication has therapeutic potential. Strategies include inhibiting exosome biogenesis and release using GW4869 or blocking Rab GTPases, blocking exosome uptake, and modulating oncogenic RNA cargo using antisense oligonucleotides, RNA interference, or CRISPR/Cas13-mediated RNA editing. Engineered exosomes also serve as natural, biocompatible carriers for the therapeutic delivery of siRNAs, miRNA mimics, mRNAs, or CRISPR components, offering improved stability, specificity, and reduced immunogenicity compared to synthetic counterparts. There are significant translational challenges, including large-scale manufacturing, purification, standardization, and biosafety testing, despite promising preclinical and early clinical results. In summary, comprehending and implementing post-transcriptional oncogene regulation via exosomes is a transformative strategy in precision oncology, creating new opportunities in targeted diagnosis, prognostication, and advanced cancer therapies.

Indexed as

ExosomeslncRNAmiRNAOncogene modulationPost-transcriptional regulationTumor microenvironment

Identifiers

PMID42176156
PMCPMC13376311

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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.