Evidence mapPaperPMID 41559804Full record

ReviewCell communication and signaling : CCS2026

Large extracellular vesicles and blebbisomes in cancer: emerging and translational opportunities highlights.

Xin Zhang, Jianan Zhe, Changling Duan, Xinyi Wei, Zhong He, Chengran Shi, Lei Yuan, Hao Wen, Wei Bao, Qiong Fan

Abstract readReview
In one paragraph

Review in Cell communication and signaling : CCS, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Condensates on the Move: Midbody Remnants as Large, Translation-Competent Extracellular Vesicles.BioEssays : news and reviews in molecular, cellular and developmental biology · 2026
    Review
  2. 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.

Xin Zhang *Department of Gynecologic Oncology, Shanghai Key Laboratory of Embryo Original Diseases, The International Peace Maternity and Child Health Hospital, Shanghai Jiao Tong University School of Medicine, No. 910, Hengshan Road, Shanghai, 200030, China.
Jianan Zhe *Department of Gynecologic Oncology, Shanghai Key Laboratory of Embryo Original Diseases, The International Peace Maternity and Child Health Hospital, Shanghai Jiao Tong University School of Medicine, No. 910, Hengshan Road, Shanghai, 200030, China.
Changling Duan *Department of Gynecologic Oncology, Shanghai Geriatric Medical Center, Shanghai, 201100, China.
Xinyi WeiDepartment of Gynecologic Oncology, Shanghai Key Laboratory of Embryo Original Diseases, The International Peace Maternity and Child Health Hospital, Shanghai Jiao Tong University School of Medicine, No. 910, Hengshan Road, Shanghai, 200030, China.
Zhong HeDepartment of Gynecologic Oncology, Shanghai Key Laboratory of Embryo Original Diseases, The International Peace Maternity and Child Health Hospital, Shanghai Jiao Tong University School of Medicine, No. 910, Hengshan Road, Shanghai, 200030, China.
Chengran ShiDepartment of Gynecologic Oncology, Shanghai Key Laboratory of Embryo Original Diseases, The International Peace Maternity and Child Health Hospital, Shanghai Jiao Tong University School of Medicine, No. 910, Hengshan Road, Shanghai, 200030, China.
Lei YuanDepartment of Gynecologic Oncology, Obstetrics and Gynecology Hospital, Fudan University, Shanghai, 200001, China.
Hao WenDepartment of Gynecologic Oncology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Wei BaoDepartment of Gynecology, Shanghai Key Laboratory of Maternal Fetal Medicine, Shanghai Institute of Maternal-Fetal Medicine and Gynecologic Oncology, Shanghai First Maternity and Infant Hospital, School of Medicine, Tongji University, Shanghai, 200092, China. forever_chipper@hotmail.com.
Qiong FanDepartment of Gynecologic Oncology, Shanghai Key Laboratory of Embryo Original Diseases, The International Peace Maternity and Child Health Hospital, Shanghai Jiao Tong University School of Medicine, No. 910, Hengshan Road, Shanghai, 200030, China. sailajoan@hotmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Large extracellular vesicles (lEVs), particularly the recently identified blebbisomes, are emerging as critical mediators of tumor progression and intercellular communication. Compared with small vesicles, lEVs exhibit pronounced heterogeneity in size, cargo composition, and mechanisms of biogenesis. While EVs of all sizes can carry proteins, nucleic acids, lipids, and metabolites, lEVs more frequently encapsulate bulky cargos-including intact organelles such as mitochondria-reflecting their size-enabled loading capacity rather than a feature unique to lEVs. These characteristics position lEVs as key regulators of immune responses, metabolic reprogramming, and the establishment of pre-metastatic niches within the tumor microenvironment. Blebbisomes, distinguished by their dynamic membrane behavior, bidirectional cargo transfer, and high expression of immunosuppressive molecules, represent a novel paradigm in extracellular communication. However, challenges persist in defining lEV subtypes, achieving efficient purification and isolation, and accurately tracking their behavior in vivo. This review systematically summarizes recent advances in lEV research in tumor biology, highlights the distinctive functions of blebbisomes, and examines their translational potential in diagnostics and therapy. Key knowledge gaps are identified, including the need for single-vesicle multi-omics, advanced lipidomics, and engineered analytical platforms. We advocate for expanded investigation into lEVs as promising targets and tools in precision oncology.

Indexed as

Extracellular VesiclesNeoplasmsTranslational Research, BiomedicalAnimalsCell CommunicationHumansTumor MicroenvironmentApoptotic bodiesBiogenesis and regulationBlebbisomesCargo and functionDrug delivery vehiclesExophersImmune evasionImmunotherapy targetsLarge extracellular vesiclesLarge oncosomesLiquid biopsyLocal invasionMicrovesiclesMidbody remnantsMigrasomesTumor immunologyTumor microenvironment

Identifiers

PMID41559804
PMCPMC12905855

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.