Evidence map›Paper›PMID 38424607›Full record

ReviewCell communication and signaling : CCS2024

Exosomes derived from programmed cell death: mechanism and biological significance.

Min Xiong, Zhen Chen, Jiaqi Tian, Yanjie Peng, Dandan Song, Lin Zhang, Yulan Jin

Abstract readReview
In one paragraph

Review in Cell communication and signaling : CCS, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing 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

30 citing papers in PubMed.

  1. Article
  2. Review
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  11. Article
  12. Pandora's Box of AML: HowBiomedicines · 2025
    Review
  13. Nanomedicine (London, England) · 2025
    Article
  14. Article
  15. Article
  16. Article
  17. Circulating Extracellular Vesicles in Cardiovascular Disease.International journal of molecular sciences · 2025
    Review
  18. Review
  19. Review
  20. Article
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

7 authors.

Min XiongSchool of Public Health, North China University of Science and Technology, Tangshan, 063000, China.
Zhen ChenSchool of Public Health, Weifang Medical University, Weifang, 261000, China.
Jiaqi TianClinical Medical Research Center for Women and Children Diseases, Key Laboratory of Birth Regulation and Control Technology of National Health Commission of China, Shandong Provincial Maternal and Child Health Care Hospital Affiliated to Qingdao University, Jinan, 250001, China.
Yanjie PengClinical Medical Research Center for Women and Children Diseases, Key Laboratory of Birth Regulation and Control Technology of National Health Commission of China, Shandong Provincial Maternal and Child Health Care Hospital Affiliated to Qingdao University, Jinan, 250001, China.
Dandan SongClinical Medical Research Center for Women and Children Diseases, Key Laboratory of Birth Regulation and Control Technology of National Health Commission of China, Shandong Provincial Maternal and Child Health Care Hospital Affiliated to Qingdao University, Jinan, 250001, China. songdandan1872@163.com.
Lin ZhangClinical Medical Research Center for Women and Children Diseases, Key Laboratory of Birth Regulation and Control Technology of National Health Commission of China, Shandong Provincial Maternal and Child Health Care Hospital Affiliated to Qingdao University, Jinan, 250001, China. zhanglin8901@sdu.edu.cn.
Yulan JinSchool of Public Health, North China University of Science and Technology, Tangshan, 063000, China. 13932579151@163.com.

Funding

Maternal and Child Health Association of Shandong Province YJKY2022-026National Natural Science Foundation of China No. 82003405Natural Science Foundation of Shandong Province ZR2020QH290Natural Science Foundation of Shandong Province ZR2022QH339Taishan Scholar Program of Shandong Province No. tsqn202211359
6 · The paper itself

Abstract

Exosomes are nanoscale extracellular vesicles present in bodily fluids that mediate intercellular communication by transferring bioactive molecules, thereby regulating a range of physiological and pathological processes. Exosomes can be secreted from nearly all cell types, and the biological function of exosomes is heterogeneous and depends on the donor cell type and state. Recent research has revealed that the levels of exosomes released from the endosomal system increase in cells undergoing programmed cell death. These exosomes play crucial roles in diseases, such as inflammation, tumors, and autoimmune diseases. However, there is currently a lack of systematic research on the differences in the biogenesis, secretion mechanisms, and composition of exosomes under different programmed cell death modalities. This review underscores the potential of exosomes as vital mediators of programmed cell death processes, highlighting the interconnection between exosome biosynthesis and the regulatory mechanisms governing cell death processes. Furthermore, we accentuate the prospect of leveraging exosomes for the development of innovative biomarkers and therapeutic strategies across various diseases.

Indexed as

ExosomesExtracellular VesiclesApoptosisBiomarkersCell CommunicationBiomarkersBiogenesisExosomeProgrammed cell deathRegulatory mechanisms

Identifiers

PMID38424607
PMCPMC10905887

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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.