Evidence map›Paper›PMID 15572682›Full record

ArticleMolecular and cellular biology2004

Functional genetic screen for genes involved in senescence: role of Tid1, a homologue of the Drosophila tumor suppressor l(2)tid, in senescence and cell survival.

Marina Tarunina, Lynsey Alger, Grace Chu, Karl Munger, Andrei Gudkov, Parmjit S Jat

Abstract read
In one paragraph

Article in Molecular and cellular biology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.0field-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

17 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. The one thousand and one chaperones of the NF-κB pathway.Cellular and molecular life sciences : CMLS · 2020
    Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Novel regulators of the systemic response to lipopolysaccharide.American journal of respiratory cell and molecular biology · 2011
    Article
  14. Activation of Erk by sonic hedgehog independent of canonical hedgehog signalling.The international journal of biochemistry & cell biology · 2010
    Article
  15. Review
  16. Multi-faceted role of HSP40 in cancer.Clinical & experimental metastasis · 2009
    Review
  17. 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

6 authors at 4 institutions in 3 countries.

Marina TaruninaLudwig Institute for Cancer Research, 91 Riding House St., London W1W 7BS, United Kingdom.
Lynsey Alger
Grace Chu
Karl Munger
Andrei Gudkov
Parmjit S Jat
Ludwig Cancer Research · BECleveland Clinic · USDana-Farber/Harvard Cancer Center · USUniversity College London · GB

Funding

GENETIC ELEMENTS TRANSFORMING MOUSE FIBROBLASTSR01CA060730 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI GUDKOV, ANDREI V · 1994 to 2009
$2.6M
NCI NIH HHS CA 60730NCI NIH HHS R01 CA060730
6 · The paper itself

Abstract

We performed a genetic suppressor element screen to identify genes whose inhibition bypasses cellular senescence. A normalized library of fragmented cDNAs was used to select for elements that promote immortalization of rat embryo fibroblasts. Fragments isolated by the screen include those with homology to genes that function in intracellular signaling, cellular adhesion and contact, protein degradation, and apoptosis. They include mouse Tid1, a homologue of the Drosophila tumor suppressor gene l(2)tid, recently implicated in modulation of apoptosis as well as gamma interferon and NF-kappaB signaling. We show that GSE-Tid1 enhances immortalization by human papillomavirus E7 and simian virus 40 T antigen and cooperates with activated ras for transformation. Expression of Tid1 is upregulated upon cellular senescence in rat and mouse embryo fibroblasts and premature senescence of REF52 cells triggered by activated ras. In accordance with this, spontaneous immortalization of rat embryo fibroblasts is suppressed upon ectopic expression of Tid1. Modulation of endogenous Tid1 activity by GSE-Tid1 or Tid1-specific RNA interference alleviates the suppression of tumor necrosis factor alpha-induced NF-kappaB activity by Tid1. We also show that NF-kappaB sequence-specific binding is strongly downregulated upon senescence in rat embryo fibroblasts. We therefore propose that Tid1 contributes to senescence by acting as a repressor of NF-kappaB signaling.

Indexed as

AnimalsAnti-Bacterial AgentsCells, CulturedCell SurvivalCellular SenescenceElectrophoretic Mobility Shift AssayEmbryo, MammalianFibroblastsGenes, ReporterGentamicinsHeat-Shock ProteinsHSP40 Heat-Shock ProteinsLuciferasesMiceMice, Inbred C57BLModels, BiologicalAnti-Bacterial Agentsantibiotic G 418Dnaja3 protein, mouseGentamicinsHeat-Shock ProteinsHSP40 Heat-Shock ProteinsLuciferasesMolecular ChaperonesNF-kappa BProteinsRNATumor Necrosis Factor-alphaTumor Suppressor Proteins

Identifiers

PMID15572682
PMCPMC533960
OpenAlexW2044832154

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.