Evidence map›Paper›PMID 38255300›Full record

ArticleBiomedicines2024

Sialidase NEU3 Contributes to the Invasiveness of Bladder Cancer.

Takeo Tatsuta, Jun Ito, Koji Yamamoto, Shigeki Sugawara, Masahiro Hosono, Makoto Sato, Taeko Miyagi

Open access · goldAbstract read
In one paragraph

Article in Biomedicines, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

7 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Degradation System: Sialidase.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  3. Review
  4. Review
  5. Review
  6. Review
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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 3 institutions in 1 country.

Takeo TatsutaDivision of Cell Recognition Study, Tohoku Medical and Pharmaceutical University, Sendai 981-8558, Japan.
Jun ItoDepartment of Urology, Faculty of Medicine, Tohoku Medical and Pharmaceutical University, Sendai 983-8536, Japan.
Koji YamamotoFaculty of Health and Medical Care, Saitama Medical University, Saitama 350-0496, Japan.
Shigeki SugawaraDivision of Cell Recognition Study, Tohoku Medical and Pharmaceutical University, Sendai 981-8558, Japan.ORCID 0000-0001-8806-5973
Masahiro HosonoDivision of Cell Recognition Study, Tohoku Medical and Pharmaceutical University, Sendai 981-8558, Japan.ORCID 0000-0003-0663-5560
Makoto SatoDepartment of Urology, Faculty of Medicine, Tohoku Medical and Pharmaceutical University, Sendai 983-8536, Japan.
Taeko MiyagiDivision of Cancer Chemotherapy, Miyagi Cancer Center Research Institute, Natori 981-1293, Japan.
Tohoku Medical and Pharmaceutical University · JPMiyagi Prefectural Hospital Organization · JPSaitama Medical University · JP

Funding

Japan Society for the Promotion of Science 21K07198
6 · The paper itself

Abstract

Bladder cancer is the 10th most commonly diagnosed cancer worldwide. The current standard treatment for advanced bladder cancer is neoadjuvant cisplatin (NAC)-based chemotherapy followed by cystectomy. However, the response rate to chemotherapy is only 50%, owing to cisplatin resistance, and there is a need for novel therapies. Because the invasiveness of bladder cancer greatly influences patient prognosis, a mechanistic analysis of the invasive function can lead to therapeutic targets. Sialidases, which remove sialic acid residues from the nonreducing ends of sugar chains and catalyze the initial reaction in the degradation of sugar chains, are predicted to be involved in cell invasion and motility. However, the involvement of sialidases in bladder cancer, especially their relationship with the invasive ability, remains unclear. Here, using patient tissues and multiple bladder cancer cell lines, we show that the sialidase

Indexed as

bladder cancerinvasionsialidase

Identifiers

PMID38255300
PMCPMC10813053
OpenAlexW4390912921

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.