Evidence map›Paper›PMID 31301084›Full record

ArticleCancer science2019

Mucin 21 is a key molecule involved in the incohesive growth pattern in lung adenocarcinoma.

Taichiro Yoshimoto, Daisuke Matsubara, Manabu Soda, Toshihide Ueno, Yusuke Amano, Atsushi Kihara, Takashi Sakatani, Tomoyuki Nakano, Tomoki Shibano, Shunsuke Endo and 6 more

Abstract readCase Reports
In one paragraph

Article in Cancer science, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. MUC21: a new target for tumor treatment.Frontiers in oncology · 2024
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Unique Glycoform-Dependent Monoclonal Antibodies for Mouse Mucin 21.International journal of molecular sciences · 2022
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. DifferentialOncology reports · 2021
    Observational
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

16 authors.

Taichiro YoshimotoDepartment of Integrative Pathology, Jichi Medical University, Japan.ORCID https://orcid.org/0000-0002-4714-5261
Daisuke MatsubaraDepartment of Integrative Pathology, Jichi Medical University, Japan.
Manabu SodaDepartment of Cellular Signaling, The University of Tokyo, Japan.
Toshihide UenoDepartment of Cellular Signaling, The University of Tokyo, Japan.
Yusuke AmanoDepartment of Integrative Pathology, Jichi Medical University, Japan.
Atsushi KiharaDepartment of Integrative Pathology, Jichi Medical University, Japan.
Takashi SakataniDepartment of Diagnostic Pathology, Nippon Medical School Hospital, Japan.
Tomoyuki NakanoDepartment of Thoracic Surgery, Jichi Medical University, Japan.
Tomoki ShibanoDepartment of Thoracic Surgery, Jichi Medical University, Japan.
Shunsuke EndoDepartment of Thoracic Surgery, Jichi Medical University, Japan.
Koichi HagiwaraDivision of Pulmonary Medicine, Department of Internal Medicine, Jichi Medical University, Japan.
Masashi FukayamaHuman Pathology, Graduate School of Medicine, The University of Tokyo, Japan.
Kaori Denda-NagaiDivision of Glycobiologics, Intractable Disease Research Center, Juntendo University, Japan.
Tatsuro IrimuraDivision of Glycobiologics, Intractable Disease Research Center, Juntendo University, Japan.
Hiroyuki ManoDepartment of Cellular Signaling, The University of Tokyo, Japan.
Toshiro NikiDepartment of Integrative Pathology, Jichi Medical University, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Decreased cell adhesion has been reported as a significant negative prognostic factor of lung cancer. However, the molecular mechanisms responsible for the cell incohesiveness in lung cancer have not yet been elucidated in detail. We herein describe a rare histological variant of lung adenocarcinoma consisting almost entirely of individual cancer cells spreading in alveolar spaces in an incohesive pattern. A whole exome analysis of this case showed no genomic abnormalities in CDH1 or other genes encoding cell adhesion molecules. However, whole mRNA sequencing revealed that this case had an extremely high expression level of mucin 21 (MUC21), a mucin molecule that was previously shown to inhibit cell-cell and cell-matrix adhesion. The strong membranous expression of MUC21 was found on cancer cells using mAbs recognizing different O-glycosylated forms of MUC21. An immunohistochemical analysis of an unselected series of lung adenocarcinoma confirmed that the strong membranous expression of MUC21 correlated with incohesiveness. Thus, MUC21 could be a promising biomarker with potential diagnostic and therapeutic applications for lung adenocarcinoma showing cell incohesiveness.

Indexed as

Adenocarcinoma of LungAgedAntigens, CDCadherinsExome SequencingFemaleGene Expression ProfilingHumansLungLung NeoplasmsMembrane GlycoproteinsMucinsTomography, X-Ray ComputedAntigens, CDCadherinsCDH1 protein, humanMembrane GlycoproteinsMUC21 protein, humanMucinsadenocarcinomacell adhesionlung cancerMUC21STAS

Identifiers

PMID31301084
PMCPMC6726699

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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.