Evidence map›Paper›PMID 26470851›Full record

ArticleCancer science2015

Upregulation of sialidase NEU3 in head and neck squamous cell carcinoma associated with lymph node metastasis.

Kiyoto Shiga, Kohta Takahashi, Ikuro Sato, Kengo Kato, Shigeru Saijo, Setsuko Moriya, Masahiro Hosono, Taeko Miyagi

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2015. 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
1.5field-weighted citation impact, top 18% 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, 34 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Sialidase Inhibitors with Different Mechanisms.Journal of medicinal chemistry · 2022
    Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Gangliosides as Signaling Regulators in Cancer.International journal of molecular sciences · 2021
    Review
  11. Review
  12. Review
  13. 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

8 authors at 2 institutions in 1 country.

Kiyoto ShigaDepartment of Otolaryngology-Head and Neck Surgery, Iwate Medical University, Morioka, Japan.
Kohta TakahashiDivision of Cancer Glycosylation Research, Tohoku Pharmaceutical University, Sendai, Japan.
Ikuro SatoDepartment of Pathology, Miyagi Cancer Center, Natori, Japan.
Kengo KatoDepartment of Head and Neck Surgery, Miyagi Cancer Center, Natori, Japan.
Shigeru SaijoDepartment of Head and Neck Surgery, Miyagi Cancer Center, Natori, Japan.
Setsuko MoriyaDivision of Cancer Glycosylation Research, Tohoku Pharmaceutical University, Sendai, Japan.
Masahiro HosonoDivision of Cell Recognition Study, Institute of Molecular Biomembrane and Glycobiology, Tohoku Pharmaceutical University, Sendai, Japan.
Taeko MiyagiDivision of Cancer Glycosylation Research, Tohoku Pharmaceutical University, Sendai, Japan.
Miyagi Prefectural Hospital Organization · JPTohoku Medical and Pharmaceutical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Regional lymph node metastasis in head and neck squamous cell carcinoma (HNSCC) is a crucial event for its progression, associated with a high rate of mortality. Sialidase, a key enzyme for the regulation of cellular sialic acids through catalyzing the initial step of degradation of glycoproteins and glycolipids, has been implicated in cancer progression. To facilitate the development of novel treatments for HNSCC, we have investigated whether sialidase is involved in the progression of this cancer. We found plasma membrane-associated sialidase (NEU3) to be significantly upregulated in tumor compared to non-tumor tissues; particularly, an increase in its mRNA levels was significantly associated with lymph node metastasis. To understand the mechanisms, we analyzed the NEU3-mediated effects on the malignant phenotype using squamous carcinoma HSC-2 and SAS cells. NEU3 promoted cell motility and invasion, accompanied by the increased expression of MMP-9, whereas NEU3 silencing or the activity-null mutant did not. NEU3 enhanced phosphorylation of epidermal growth factor receptor (EGFR), and an EGFR inhibitor, AG1478, abrogated the NEU3-induced MMP9 augmentation. These findings identify NEU3 as a participant in HNSCC progression through the regulation of EGFR signaling and thus as a potential target for inhibiting EGFR-mediated tumor progression.

Indexed as

AdultAgedAged, 80 and overBiomarkers, TumorCarcinoma, Squamous CellChromatography, Thin LayerDisease ProgressionFemaleHead and Neck NeoplasmsHumansImmunoblottingImmunohistochemistryLymphatic MetastasisMaleMiddle AgedNeuraminidaseBiomarkers, TumorNeu3 protein, humanNeuraminidaseRNA, Small InterferingEpidermal growth factor receptorhead and neck squamous cell carcinomalymph node metastasisMMP9sialidase

Identifiers

PMID26470851
PMCPMC4714679
OpenAlexW2096469690

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.