Evidence map›Paper›PMID 11401315›Full record

ArticleBritish journal of cancer2001

Modulation of TcR/CD3-zeta chain expression by a circulating factor derived from ovarian cancer patients.

D D Taylor, D P Bender, Gerçel-Taylor C, J Stanson, T L Whiteside

Abstract read
In one paragraph

Article in British journal of cancer, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Trial
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  6. Article
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  8. Article
  9. Covert operations: cancer's many subversive tactics in overcoming host defenses.Transactions of the American Clinical and Climatological Association · 2013
    Article
  10. Article
  11. The mechanisms by which polyamines accelerate tumor spread.Journal of experimental & clinical cancer research : CR · 2011
    Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  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

5 authors.

D D TaylorDepartment of Obstetrics, University of Louisville School of Medicine, Louisville, KY 40292, USA.
D P Bender
Gerçel-Taylor C
J Stanson
T L Whiteside

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In women with ovarian cancer, suppression of components of the immune system may promote tumour development. Previous studies in ovarian cancer have demonstrated that decreased expression and function of the T-cell receptor (TcR)-associated signal transducing zeta-chain correlates with deficient immune responsiveness of T cells. In this study, sera and ascitic fluids obtained from woman with advanced ovarian cancer were found to suppress the expression of TcR-associated zeta chain. This suppression of zeta chain expression was dose-dependent and was not observed with biologic fluids obtained from healthy women. The factor responsible for the loss of zeta chain was purified from ascites and characterized as a protein with an appropriate molecular weight of 14 kD. Suppression of T-cell TcR-zeta was specific, since neither lck nor ZAP-70 expression was affected, while zeta chain was almost completely suppressed. This selective suppression of TcR-zeta expression by the 14 kD ascites-derived factor was shown to operate at the mRNA level. By defining the mechanism through which this protein modulates TcR-zeta chain levels, it might be possible to ultimately prevent the suppressive influences of the tumour microenvironment and restor immune competence in patients with ovarian carcinoma.

Indexed as

Immunosuppression TherapyAdultAscitesBlotting, WesternCarcinomaCase-Control StudiesFemaleGene Expression Regulation, NeoplasticHumansImmunocompetenceMembrane ProteinsOvarian NeoplasmsProteinsReceptor-CD3 Complex, Antigen, T-CellReceptors, Antigen, T-Cellantigen T cell receptor, zeta chainMembrane ProteinsProteinsReceptor-CD3 Complex, Antigen, T-CellReceptors, Antigen, T-Cell

Identifiers

PMID11401315
PMCPMC2363678

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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.