Evidence map›Paper›PMID 28166442›Full record

ReviewCell adhesion & migration2017

Exosomes in cancer theranostic: Diamonds in the rough.

Marine Cordonnier, Gaëtan Chanteloup, Nicolas Isambert, Renaud Seigneuric, Pierre Fumoleau, Carmen Garrido, Jessica Gobbo

Open access · goldAbstract readReview
In one paragraph

Review in Cell adhesion & migration, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
3.7field-weighted citation impact, top 6% of its field
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

43 citing papers in PubMed, 81 citations in OpenAlex.

  1. Review
  2. Review
  3. New uses of halofuginone to treat cancer.Journal of pharmaceutical analysis · 2025
    Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Microfluidic Approaches for Affinity-Based Exosome Separation.International journal of molecular sciences · 2022
    Review
  15. Review
  16. Molecular and Circulating Biomarkers in Patients with Glioblastoma.International journal of molecular sciences · 2022
    Review
  17. Review
  18. Exosome-Laden Hydrogels: A Novel Cell-free Strategy forFrontiers in bioengineering and biotechnology · 2022
    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 at 3 institutions in 1 country.

Marine Cordonniera INSERM, UMR 866, Laboratoire d'Excellence LipSTIC , Dijon , France.
Gaëtan Chanteloupa INSERM, UMR 866, Laboratoire d'Excellence LipSTIC , Dijon , France.
Nicolas Isamberta INSERM, UMR 866, Laboratoire d'Excellence LipSTIC , Dijon , France.
Renaud Seigneurica INSERM, UMR 866, Laboratoire d'Excellence LipSTIC , Dijon , France.
Pierre Fumoleauc Department of Medical Oncology , Georges-François Leclerc Centre , Dijon , France.
Carmen Garridoa INSERM, UMR 866, Laboratoire d'Excellence LipSTIC , Dijon , France.
Jessica Gobboa INSERM, UMR 866, Laboratoire d'Excellence LipSTIC , Dijon , France.
Centre Georges François Leclerc · FRInserm · FRUniversité de Bourgogne · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During the last 10 years, exosomes, which are small vesicles of 50-200 nm diameter of endosomal origin, have aroused a great interest in the scientific and clinical community for their roles in intercellular communication in almost all physiological and pathological processes. Most cells can potentially release these nanovesicles that share with the parent cell a similar lipid bilayer with transmembrane proteins and a panel of enclosed soluble proteins such as heat shock proteins and genetic material, thus acting as potential nanoshuttles of biomarkers. Exosomes surface proteins allow their targeting and capture by recipient cells, while the exosomes' content can modify the physiological state of recipient cells. Tumor derived exosomes by interacting with other cells of the tumor microenvironment modulate tumor progression, angiogenic switch, metastasis, and immune escape. Targeting tumor-derived exosomes might be an interesting approach in cancer therapy. Furthermore, because a key issue to improve cancer patients' outcome relies on earlier cancer diagnosis (metastases, as opposed to the primary tumor, are responsible for most cancer deaths) exosomes have been put forward as promising biomarker candidates for cancer diagnosis and prognosis. This review summarizes the roles of exosomes in cancer and clinical interest, focusing on the importance of exosomal heat shock proteins (HSP). The challenges of clinical translation of HSP-exosomes as therapeutic targets and biomarkers for early cancer detection are also discussed.

Indexed as

AnimalsBiomarkers, TumorDrug Delivery SystemsExosomesHumansModels, BiologicalNeoplasmsTheranostic NanomedicineBiomarkers, Tumorcancer diagnosiscancer therapyexosomesheat shock proteins

Identifiers

PMID28166442
PMCPMC5351734
OpenAlexW2586804218

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.