Evidence map›Paper›PMID 37096775›Full record

ArticleCancer medicine2023

Phosphatidylcholine in bile-derived small extracellular vesicles as a novel biomarker of cholangiocarcinoma.

Ryuta Muraki, Yoshifumi Morita, Shinya Ida, Ryo Kitajima, Satoru Furuhashi, Makoto Takeda, Hirotoshi Kikuchi, Yoshihiro Hiramatsu, Yusuke Takanashi, Yasushi Hamaya and 8 more

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 10% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Diagnostic and prognostic significance of circulating extracellular vesicles in gastrointestinal cancers.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
  4. Article
  5. Review
  6. Review
  7. Mutational Analysis of Bile Cell-Free DNA in Primary Sclerosing Cholangitis: A Pilot Study.Liver international : official journal of the International Association for the Study of the Liver · 2025
    Article
  8. Review
  9. Article
  10. Review
  11. 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

18 authors at 3 institutions in 2 countries.

Ryuta MurakiSecond Department of Surgery, Hamamatsu University School of Medicine, Hamamatsu, Japan.ORCID 0000-0001-9261-3506
Yoshifumi MoritaSecond Department of Surgery, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Shinya IdaSecond Department of Surgery, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Ryo KitajimaSecond Department of Surgery, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Satoru FuruhashiSecond Department of Surgery, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Makoto TakedaSecond Department of Surgery, Hamamatsu University School of Medicine, Hamamatsu, Japan.ORCID 0000-0003-1523-1103
Hirotoshi KikuchiSecond Department of Surgery, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Yoshihiro HiramatsuSecond Department of Surgery, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Yusuke TakanashiFirst Department of Surgery, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Yasushi HamayaFirst Department of Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Ken SugimotoFirst Department of Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Jun ItoSecond Department of Internal Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Kazuhito KawataSecond Department of Internal Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Hideya KawasakiPreeminent Medical Photonics Education & Research Center, Institute for NanoSuit Research, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Tomohito SatoDepartment of Cellular and Molecular Anatomy, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Tomoaki KahyoDepartment of Cellular and Molecular Anatomy, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Mitsutoshi SetouDepartment of Cellular and Molecular Anatomy, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Hiroya TakeuchiSecond Department of Surgery, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Hamamatsu University School of Medicine · JPHamamatsu University · JPHamamatsu Photonics (Japan) · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOwing to the lack of definite diagnostic modalities, it is challenging to distinguish malignant cases of cholangiocarcinoma (CCA), which often causes biliary tract obstruction, from benign ones. Here, we investigated a novel lipid biomarker of CCA in bile-derived small extracellular vesicles (sEVs) and developed a simple detection method for clinical application.

methodsBile samples from seven patients with malignant diseases (hilar CCA = 4, distal CCA = 3) and eight patients with benign diseases (gallstones = 6, primary sclerosing cholangitis = 1, autoimmune pancreatitis = 1) were collected through a nasal biliary drainage tube. sEVs were isolated via serial ultracentrifugation and characterized using nanoparticle tracking analysis, transmission electron microscopy, and immunoblotting (with CD9, CD63, CD81, and TSG101). Comprehensive lipidomic analysis was performed using liquid chromatography-tandem mass spectrometry. Using a measurement kit, we further confirmed whether lipid concentrations could be used as a potential CCA marker.

resultsLipidomic analysis of bile sEVs in the two groups identified 209 significantly increased lipid species in the malignant group. When focusing on lipid class, phosphatidylcholine (PC) level was 4.98-fold higher in the malignant group than in the benign group (P = 0.037). The receiver operating characteristic (ROC) curve showed a sensitivity of 71.4%, a specificity of 100%, and an area under the curve (AUC) of 0.857 (95% confidence interval [CI]:0.643-1.000). Using a PC assay kit, the ROC curve showed a cutoff value of 16.1 μg/mL, a sensitivity of 71.4%, a specificity of 100%, and an AUC of 0.839 (95% CI: 0.620-1.000).

conclusionPC level in sEVs from human bile is a potential diagnostic marker for CCA and can be assessed by a commercially available assay kit.

Indexed as

Bile Duct NeoplasmsCholangiocarcinomaExtracellular VesiclesBileBile Ducts, IntrahepaticBiomarkersBiomarkers, TumorHumansPhosphatidylcholinesBiomarkersBiomarkers, TumorPhosphatidylcholinesbilebiomarkercholangiocarcinomaextracellular vesiclephosphatidylcholine

Identifiers

PMID37096775
PMCPMC10315768
OpenAlexW4366986985

What OpenQuestion holds

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LicenceCC BY
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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.