Evidence map›Paper›PMID 42261358›Full record

ArticleInternational journal of nanomedicine2026

Royal Jelly-Derived Extracellular Vesicles: Key Bioactive Components Mediating Anti-Hepatocellular Carcinoma Activity.

Xuepeng Chi, Lingyu Jia, Ying Wang, Chao Liu, Shuai Wang, Zhenguo Liu, Ge Zhang, Baohua Xu

Abstract read
In one paragraph

Article in International journal of nanomedicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

8 authors.

Xuepeng ChiKey Laboratory of Efficient Utilization of Non-Grain Feed Resources (Co-Construction by Ministry and Province), Shandong Agricultural University, Tai'an, Shandong, People's Republic of China.
Lingyu JiaKey Laboratory of Efficient Utilization of Non-Grain Feed Resources (Co-Construction by Ministry and Province), Shandong Agricultural University, Tai'an, Shandong, People's Republic of China.
Ying WangKey Laboratory of Efficient Utilization of Non-Grain Feed Resources (Co-Construction by Ministry and Province), Shandong Agricultural University, Tai'an, Shandong, People's Republic of China.
Chao LiuDepartment of Minimally Invasive Oncology, Tai'an City Central Hospital, Tai'an, Shandong, People's Republic of China.
Shuai WangBeekeeping Division, Shandong Provincial Animal Husbandry and Veterinary Bureau, Ji'nan, Shandong, People's Republic of China.
Zhenguo LiuKey Laboratory of Efficient Utilization of Non-Grain Feed Resources (Co-Construction by Ministry and Province), Shandong Agricultural University, Tai'an, Shandong, People's Republic of China.
Ge ZhangKey Laboratory of Efficient Utilization of Non-Grain Feed Resources (Co-Construction by Ministry and Province), Shandong Agricultural University, Tai'an, Shandong, People's Republic of China.
Baohua XuKey Laboratory of Efficient Utilization of Non-Grain Feed Resources (Co-Construction by Ministry and Province), Shandong Agricultural University, Tai'an, Shandong, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: To investigate the role of royal jelly derived extracellular vesicles (RJEVs) as key active components contributing to the anti-hepatocellular carcinoma (HCC) effects of royal jelly and to elucidate the underlying mechanisms. Patients and Methods: This study used H22 tumor-bearing mice as an in vivo model. RJEVs were isolated and identified and their effects were evaluated after oral administration. Analyses included the assessment of liver-targeting properties, immune and antioxidant responses, gut microbiota composition (specifically Muribaculaceae abundance), and short-chain fatty acid metabolism. This study also examined the influence of RJEVs on translation-related signaling networks and the Phosphatidylinositol 3-kinase (PI3K) / Protein Kinase B (AKT) signaling pathway to determine their role in promoting tumor cell apoptosis. Results: Orally administered RJEVs exhibited liver-accumulating properties in H22 tumor-bearing mice and demonstrated moderate antitumor efficacy. They enhanced immune and antioxidant responses, increased the abundance of Muribaculaceae, modulated gut microbiota composition, and improved short-chain fatty acid metabolism. Mechanistically, RJEVs synergistically regulate translation-related signaling networks and remodel the immune microenvironment, ultimately promoting tumor cell apoptosis via the PI3K/AKT signaling pathway. Conclusion: These findings provide novel insights into the functional role of royal jelly by identifying RJEVs as important bioactive constituents that contribute to the anti-HCC effects by modulating the immune microenvironment, gut microbiota, and PI3K/AKT signaling. This offers both theoretical and methodological advances in research on the bioactive components of bee products.

Indexed as

Antineoplastic AgentsCarcinoma, HepatocellularExtracellular VesiclesFatty AcidsLiver NeoplasmsRoyal JellyAnimalsAntioxidantsApoptosisCell Line, TumorGastrointestinal MicrobiomeHumansMaleMicePhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktAntineoplastic AgentsAntioxidantsFatty AcidsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktRoyal Jellyantioxidantapoptosisgut microbiotaimmunomodulationPI3K/AKT signaling pathway

Identifiers

PMID42261358
PMCPMC13242828

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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.