Evidence map›Paper›PMID 16091761›Full record

ArticleBritish journal of cancer2005

Prognostic impact of FAS/CD95/APO-1 in urothelial cancers: decreased expression of Fas is associated with disease progression.

K Yamana, V Bilim, N Hara, T Kasahara, T Itoi, R Maruyama, T Nishiyama, K Takahashi, Y Tomita

Open access · hybridAbstract readComparative Study
In one paragraph

Article in British journal of cancer, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
4.8field-weighted citation impact, top 5% 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

27 citing papers in PubMed, 72 citations in OpenAlex.

  1. Article
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  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. The role of CD95 and CD95 ligand in cancer.Cell death and differentiation · 2015
    Review
  13. Article
  14. Article
  15. Article
  16. Prognostic value of the Fas/Fas ligand system in breast cancer.Contemporary oncology (Poznan, Poland) · 2013
    Article
  17. MMP-2 and DcR3 expression in esophageal cancer tissue and correlation with patient survival.International journal of clinical and experimental medicine · 2013
    Article
  18. Article
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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

9 authors at 2 institutions in 1 country.

K YamanaDivision of Molecular Oncology, Department of Signal Transduction Research, Niigata University Graduate School of Medical and Dental Sciences, Asahimachi 1-757, Niigata 951-8510, Japan.
V Bilim
N Hara
T Kasahara
T Itoi
R Maruyama
T Nishiyama
K Takahashi
Y Tomita
Niigata University · JPYamagata University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The death receptor Fas (Apo1/CD95) and Fas ligand (FasL) system is recognised as a major pathway for the induction of apoptosis in vivo, and antiapoptosis via its blockade plays a critical role in carcinogenesis and progression in several malignancies. However, the function of Fas-FasL system in urothelial cancer (UC) has not been elucidated. We therefore investigated the expression of Fas, FasL and Decoy receptor 3 for FasL (DcR3) in UC specimens and cell lines, and examined the cytotoxic effect of an anti-Fas-activating monoclonal antibody (mAb) in vitro. Immunohistochemical examinations of Fas-related molecules were performed on 123 UC and 30 normal urothelium surgical specimens. Normal urothelium showed Fas staining in the cell membrane and cytoplasm. In UC, less frequent Fas expression was significantly associated with a higher pathological grade (P < 0.0001), a more advanced stage (P = 0.023) and poorer prognosis (P = 0.010). Fas and the absence thereof were suggested to be crucial factors with which to select patients requiring more aggressive treatment. Moreover, low-dose anti-Fas-activating mAb sensitised resistant cells to adriamycin, and this synergistic effect could be applied in the development of new treatment strategy for UC patients with multidrug-resistant tumours.

Indexed as

AdultAgedAged, 80 and overAntibiotics, AntineoplasticApoptosisCase-Control StudiesCell MembraneCytoplasmDisease ProgressionDoxorubicinDrug Resistance, NeoplasmFas Ligand Proteinfas ReceptorFemaleFlow CytometryHumansAntibiotics, AntineoplasticDoxorubicinFASLG protein, humanFas Ligand Proteinfas ReceptorMembrane GlycoproteinsReceptors, Cell SurfaceReceptors, Tumor Necrosis FactorReceptors, Tumor Necrosis Factor, Member 6bTNFRSF6B protein, human

Identifiers

PMID16091761
PMCPMC2361597
OpenAlexW1985924296

What OpenQuestion holds

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LicenceCC BY
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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.