Evidence mapPaperPMID 41712137Full record

ReviewDiscover oncology2026

The emerging role of exosomal circRNAs in modulating apoptotic pathways and overcoming cancer therapy resistance.

Mokhtar Rejili, Najma Farahani, Farid Hashemi

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

3 authors.

Mokhtar RejiliDepartment of Biology, College of Sciences, Imam Mohammad Ibn Saud Islamic University (IMSIU), Riyadh, 11623, Saudi Arabia.
Najma FarahaniFarhikhtegan Medical Convergence Sciences Research Center, Farhikhtegan Hospital, TeMs.C, Islamic Azad University, Tehran, Iran.
Farid HashemiDepartment of Comparative Biosciences, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran. faridhashemi360@gmail.com.

Funding

the Deanship of Scientific Research at Imam Mohammad Ibn Saud Islamic University (IMSIU) grant number IMSIU-DDRSP2601
6 · The paper itself

Abstract

Exosomal circular RNAs (circRNAs) have emerged as key regulators of tumor apoptosis, with significant implications for cancer development and treatment response. These persistent, covalently closed-loop RNAs are preferentially packed into exosomes, which are nanoscale extracellular vesicles that allow cells to communicate within the tumor microenvironment. This study investigates the molecular mechanisms underlying exosomal circRNA synthesis, selective cargo sorting, and their modulatory effects on apoptotic signaling pathways in various malignancies, including hepatocellular carcinoma, lung, gastric, pancreatic, and colorectal cancers. Exosomal circRNAs regulate apoptosis primarily through microRNA sponging, interaction with RNA-binding proteins, and the encoding of functional peptides, which influence tumor cell survival, treatment resistance, and metastatic potential. We highlight recent advances in the translational potential of exosomal circRNAs as diagnostic biomarkers and therapeutic targets for overcoming apoptosis evasion in malignancies. Targeting exosomal circRNA-mediated apoptotic networks is a promising approach to precision oncology and better clinical outcomes. This review highlights the critical need for more mechanistic and clinical investigations to utilize exosome biology in cancer therapy innovation.

Indexed as

BiomarkersCancer progressionExosomal circular RNAsSignaling pathwaysTherapeutic TargetsTumor apoptosis

Identifiers

PMID41712137
PMCPMC13083682

What Socratic holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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 Socratic graph.