Evidence map›Paper›PMID 27358229›Full record

Trial reportJournal of gastroenterology2017

Wisteria floribunda agglutinin-sialylated mucin core polypeptide 1 is a sensitive biomarker for biliary tract carcinoma and intrahepatic cholangiocarcinoma: a multicenter study.

Junichi Shoda, Atsushi Matsuda, Takashi Shida, Masakazu Yamamoto, Masato Nagino, Toshio Tsuyuguchi, Takahiro Yasaka, Susumu Tazuma, Kazuhisa Uchiyama, Michiaki Unno and 4 more

Open access · hybridAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in Journal of gastroenterology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 11% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Assessment of tumor characteristics based on glycoform analysis of membrane-tethered MUC1.Laboratory investigation; a journal of technical methods and pathology · 2017
    Article
  9. 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

14 authors at 9 institutions in 1 country.

Junichi ShodaDepartment of Medical Science, Faculty of Medicine,, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki, 305-8575, Japan. shodaj@md.tsukuba.ac.jp.ORCID http://orcid.org/0000-0001-9374-994X
Atsushi MatsudaResearch Center for Medical Glycoscience (RCMG), National Institute of Advanced Industrial Science and Technology (AIST), Central 2, Tsukuba, Ibaraki, Japan.
Takashi ShidaDepartment of Medical Science, Faculty of Medicine,, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki, 305-8575, Japan.
Masakazu YamamotoDepartment of Surgery, Institute of Gastroenterology, Tokyo Women's Medical University, Tokyo, Japan.
Masato NaginoDivision of Surgical Oncology, Department of Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Toshio TsuyuguchiDepartment of Gastroenterology and Nephrology, Graduate School of Medicine, Chiba University, Chiba, Japan.
Takahiro YasakaDivision of Surgery, Nagasaki Prefectural Kamigoto Hospital, Nagasaki, Japan.
Susumu TazumaDepartment of General Internal Medicine, Hiroshima University Hospital, Hiroshima, Japan.
Kazuhisa UchiyamaDepartment of General and Gastroenterological Surgery, Osaka Medical College, Takatsuki, Osaka, Japan.
Michiaki UnnoDepartment of Surgery, Tohoku University School of Medicine, Sendai, Japan.
Nobuaki OhkohchiDepartment of Gastrointestinal Surgery, Faculty of Medicine, University of Tsukuba, Tsukuba, Ibaraki, Japan.
Yasuni NakanumaDepartment of Human Pathology, Graduate School of Medical Science, Kanazawa University, Kanazawa, Japan.
Atsushi KunoResearch Center for Medical Glycoscience (RCMG), National Institute of Advanced Industrial Science and Technology (AIST), Central 2, Tsukuba, Ibaraki, Japan.
Hisashi NarimatsuResearch Center for Medical Glycoscience (RCMG), National Institute of Advanced Industrial Science and Technology (AIST), Central 2, Tsukuba, Ibaraki, Japan.
National Institute of Advanced Industrial Science and Technology · JPUniversity of Tsukuba · JPChiba University · JPHiroshima University Hospital · JPKanazawa University · JPNagoya University · JPOsaka Medical and Pharmaceutical University · JPTohoku University · JPTokyo Women's Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWisteria floribunda agglutinin (WFA)-sialylated mucin core polypeptide 1 (MUC1) was investigated as a new glycoprotein marker for cholangiocarcinoma (CC) using glycoproteomics technologies. In this multicenter study, WFA-sialylated MUC1 levels in serum and bile samples were measured to determine their diagnostic capability in biliary tract carcinoma (BTC) and intrahepatic (Ih) CC.

methodsThe study included 244 patients with BTC, 59 patients with IhCC, 287 patients with benign biliary tract diseases, and 44 control subjects.

resultsSerum WFA-sialylated MUC1 levels were significantly higher in patients with either BTC or IhCC than in control subjects and those with benign biliary tract diseases. Patients with IhCC showed higher WFA-sialylated MUC1 levels than patients with tumors at other sites. No significant differences in WFA-sialylated MUC1 levels were found with regard to cancer stage or tissue type. Receiver operating characteristic curve analysis showed that WFA-sialylated MUC1 was superior to carbohydrate antigen 19-9 (CA19-9) and carcinoembryonic antigen (CEA) for the diagnosis of benign biliary tract diseases, BTC, and IhCC, as well as for stage I and II carcinomas. Significantly higher levels of biliary WFA-sialylated MUC1 were observed in BTC/IhCC than in benign biliary tract diseases. The diagnostic capability of biliary WFA-sialylated MUC1 was also superior to that of CA19-9, and diagnostic sensitivity was higher than that of biliary cytology for BTC/IhCC.

conclusionsWFA-sialylated MUC1 is a useful novel biomarker for BTC/IhCC. In the future, this measurement should be applied in the clinical setting.

Indexed as

AdultAgedAged, 80 and overBile Duct NeoplasmsBiliary Tract DiseasesBiliary Tract NeoplasmsBiomarkers, TumorCA-19-9 AntigenCase-Control StudiesCholangiocarcinomaFemaleHumansMaleMiddle AgedMucin-1Neoplasm StagingBiomarkers, TumorCA-19-9 AntigenMUC1 protein, humanMucin-1Plant LectinsReceptors, N-Acetylglucosaminewisteria lectinBiliary tract carcinomaBiomarkerGlycoproteomicsIntrahepatic cholangiocarcinomaMulticenter study

Identifiers

PMID27358229
PMCPMC5281651
OpenAlexW2460490434

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.