Evidence map›Paper›PMID 34808019›Full record

ArticleCancer science2022

Glycosylation of MUC6 by α1,4-linked N-acetylglucosamine enhances suppression of pancreatic cancer malignancy.

Atsuko Yuki, Chifumi Fujii, Kazuhiro Yamanoi, Hisanori Matoba, Satoru Harumiya, Masatomo Kawakubo, Jun Nakayama

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Article
  3. Multiple roles and mechanisms of MUC6 in cancer (Review).International journal of molecular medicine · 2025
    Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
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  11. Article
  12. Analysis ofJournal of Cancer · 2022
    Article
  13. Review
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 1 institution in 1 country.

Atsuko YukiDepartment of Molecular Pathology, Shinshu University School of Medicine, Matsumoto, Japan.
Chifumi FujiiDepartment of Molecular Pathology, Shinshu University School of Medicine, Matsumoto, Japan.ORCID https://orcid.org/0000-0001-8735-5274
Kazuhiro YamanoiDepartment of Molecular Pathology, Shinshu University School of Medicine, Matsumoto, Japan.ORCID https://orcid.org/0000-0002-5361-8053
Hisanori MatobaDepartment of Molecular Pathology, Shinshu University School of Medicine, Matsumoto, Japan.
Satoru HarumiyaDepartment of Molecular Pathology, Shinshu University School of Medicine, Matsumoto, Japan.
Masatomo KawakuboDepartment of Molecular Pathology, Shinshu University School of Medicine, Matsumoto, Japan.ORCID https://orcid.org/0000-0001-5106-5742
Jun NakayamaDepartment of Molecular Pathology, Shinshu University School of Medicine, Matsumoto, Japan.ORCID https://orcid.org/0000-0001-6773-2802
Shinshu University · JP

Funding

Grants-in-Aid for Scientific Research (KAKENHI) from the Japan Society for the Promotion of Science 18K08613Grants-in-Aid for Scientific Research (KAKENHI) from the Japan Society for the Promotion of Science 19H03441
6 · The paper itself

Abstract

Biomarkers for early diagnosis of pancreatic cancer are greatly needed, as the high fatality of this cancer is in part due to delayed detection. α1,4-linked N-acetylglucosamine (αGlcNAc), a unique O-glycan specific to gastric gland mucus, is biosynthesized by α1,4-N-acetylglucosaminyltransferase (α4GnT) and primarily bound at the terminal glycosylated residue to scaffold protein MUC6. We previously reported that αGlcNAc expression decreases at early stages of neoplastic pancreatic lesions, followed by decreased MUC6 expression, although functional effects of these outcomes were unknown. Here, we ectopically expressed α4GnT, the αGlcNAc biosynthetic enzyme, together with MUC6 in the human pancreatic cancer cell lines MIA PaCa-2 and PANC-1, neither of which expresses α4GnT and MUC6. We observed significantly suppressed proliferation in both lines following coexpression of α4GnT and MUC6. Moreover, cellular motility decreased following MUC6 ectopic expression, an effect enhanced by cotransduction with α4GnT. MUC6 expression also attenuated invasiveness of both lines relative to controls, and this effect was also enhanced by additional α4GnT expression. We found αGlcNAc-bound MUC6 formed a complex with trefoil factor 2. Furthermore, analysis of survival curves of patients with pancreatic ductal adenocarcinoma using a gene expression database showed that samples marked by higher A4GNT or MUC6 mRNA levels were associated with relatively favorable prognosis. These results strongly suggest that αGlcNAc and MUC6 function as tumor suppressors in pancreatic cancer and that decreased expression of both may serve as a biomarker of tumor progression to pancreatic cancer.

Indexed as

AcetylglucosamineBiomarkers, TumorCarcinoma, Pancreatic DuctalCell Line, TumorCell MovementCell ProliferationGlycosylationHumansMucin-6N-AcetylglucosaminyltransferasesPancreatic NeoplasmsPrognosisRNA, MessengerTrefoil Factor-2Tumor Suppressor ProteinsAcetylglucosamineBiomarkers, TumorMUC6 protein, humanMucin-6N-AcetylglucosaminyltransferasesRNA, MessengerTFF2 protein, humanTrefoil Factor-2Tumor Suppressor Proteinsmalignant phenotypeMUC6pancreatic cancerα4GnTαGlcNAc

Identifiers

PMID34808019
PMCPMC8819301
OpenAlexW3216425481

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.