Evidence map›Paper›PMID 10491412›Full record

ArticleThe Journal of clinical investigation1999

Renal cell carcinoma-derived gangliosides suppress nuclear factor-kappaB activation in T cells.

R G Uzzo, P Rayman, V Kolenko, P E Clark, M K Cathcart, T Bloom, A C Novick, R M Bukowski, T Hamilton, J H Finke

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

32 citing papers in PubMed, 124 citations in OpenAlex.

  1. Review
  2. Lipids as Targets for Renal Cell Carcinoma Therapy.International journal of molecular sciences · 2023
    Review
  3. Review
  4. Role of Globotriaosylceramide in Physiology and Pathology.Frontiers in molecular biosciences · 2022
    Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Cutting Edge: Engineering Active IKKβ in T Cells Drives Tumor Rejection.Journal of immunology (Baltimore, Md. : 1950) · 2016
    Article
  10. Review
  11. T cell-NF-κB activation is required for tumor control in vivo.Journal for immunotherapy of cancer · 2015
    Article
  12. Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Basic research in kidney cancer.European urology · 2011
    Review
  18. Article
  19. Article
  20. 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

10 authors at 5 institutions in 2 countries.

R G UzzoDepartment of Immunology, Lerner Research Institute, Cleveland, Ohio 44195, USA.
P Rayman
V Kolenko
P E Clark
M K Cathcart
T Bloom
A C Novick
R M Bukowski
T Hamilton
J H Finke
Cleveland Clinic · USCase Comprehensive Cancer CenterCerner (United States) · USCleveland Clinic Lerner College of Medicine · USInstitute of Molecular Medicine · IN

Funding

T-CELL UNRESPONSIVENESS IN TUMORSR01CA056937 · NCI · CLEVELAND CLINIC LERNER COM-CWRU · PI FINKE, JAMES H · 1992 to 2007
$2.3M
NCI NIH HHS CA56937NCI NIH HHS R01 CA056937
6 · The paper itself

Abstract

Activation of the transcription factor nuclear factor-kappaB (NFkappaB) is impaired in T cells from patients with renal cell carcinomas (RCCs). In circulating T cells from a subset of patients with RCCs, the suppression of NFkappaB binding activity is downstream from the stimulus-induced degradation of the cytoplasmic factor IkappaBalpha. Tumor-derived soluble products from cultured RCC explants inhibit NFkappaB activity in T cells from healthy volunteers, despite a normal level of stimulus-induced IkappaBalpha degradation in these cells. The inhibitory agent has several features characteristic of a ganglioside, including sensitivity to neuraminidase but not protease treatment; hydrophobicity; and molecular weight less than 3 kDa. Indeed, we detected gangliosides in supernatants from RCC explants and not from adjacent normal kidney tissue. Gangliosides prepared from RCC supernatants, as well as the purified bovine gangliosides G(m1) and G(d1a), suppressed NFkappaB binding activity in T cells and reduced expression of the cytokines IL-2 and IFN-gamma. Taken together, our findings suggest that tumor-derived gangliosides may blunt antitumor immune responses in patients with RCCs.

Indexed as

I-kappa B ProteinsCarcinoma, Renal CellDNA-Binding ProteinsGangliosidesHumansImmunosuppressive AgentsInterferon-gammaInterleukin-2Kidney NeoplasmsNF-kappa BNF-KappaB Inhibitor alphaT-LymphocytesDNA-Binding ProteinsGangliosidesI-kappa B ProteinsImmunosuppressive AgentsInterferon-gammaInterleukin-2NF-kappa BNF-KappaB Inhibitor alphaNFKBIA protein, human

Identifiers

PMID10491412
PMCPMC408430
OpenAlexW1993396683

What OpenQuestion holds

Textmetadata
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.