Evidence map›Paper›PMID 11042692›Full record

ArticleOncogene2000

Interferon-beta induces S phase slowing via up-regulated expression of PML in squamous carcinoma cells.

S Vannucchi, Z A Percario, M V Chiantore, P Matarrese, M K Chelbi-Alix, M Fagioli, P G Pelicci, W Malorni, G Fiorucci, G Romeo and 1 more

Open access · hybridAbstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

14 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. 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

11 authors at 7 institutions in 2 countries.

S VannucchiLaboratory of Virology, Istituto Superiore di Sanità, Viale Regina Elena 299, 00161 Rome, Italy.
Z A Percario
M V Chiantore
P Matarrese
M K Chelbi-Alix
M Fagioli
P G Pelicci
W Malorni
G Fiorucci
G Romeo
E Affabris
Istituto Superiore di Sanità · ITMarconi University · ITCentre National de la Recherche Scientifique · FREuropean Institute of Oncology · ITInstitute of Biomedical Technologies · ITIstituto per le Tecnologie Didattiche · ITUniversity of Perugia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Type I Interferon (IFN) and all-trans retinoic acid (RA) inhibit cell proliferation of squamous carcinoma cell lines (SCC). Examinations of growth-affected cell populations show that SCC lines ME-180 and SiHa treated with IFN-beta undergo a specific slower progression through the S phase that seems to trigger cellular death. In combination treatment RA potentiates IFN-beta effect in SCC ME-180 but not in SiHa cell line, partially resistant to RA antiproliferative action. RA added as single agent affects cell proliferation differently by inducing a slight G1 accumulation. The IFN-beta-induced S phase lengthening parallels the increased expression of PML, a nuclear phosphoprotein specifically up-regulated at transcriptional level by IFN, whose overexpression induces cell growth inhibition and tumor suppression. We report that PML up-regulation may account for the alteration of cell cycle progression induced by IFN-beta in SCC by infecting cells with PML-PINCO recombinant retrovirus carrying the PML-3 cDNA under the control of the 5' LTR. In fact PML overexpression reproduces the IFN-beta-induced S phase lengthening. These findings provide important insight into the mechanism of tumor suppressing function of PML and could allow PML to be included in the pathways responsible for IFN-induced cell growth suppression.

Indexed as

Nuclear ProteinsAntineoplastic AgentsAntineoplastic Combined Chemotherapy ProtocolsCarcinoma, Squamous CellCell DivisionDNA, NeoplasmFemaleGene Expression Regulation, NeoplasticGrowth InhibitorsHumansInterferon Type INeoplasm ProteinsPromyelocytic Leukemia ProteinProtein IsoformsRecombinant ProteinsS PhaseAntineoplastic AgentsDNA, NeoplasmGrowth InhibitorsInterferon Type INeoplasm ProteinsNuclear ProteinsPML protein, humanPromyelocytic Leukemia ProteinProtein IsoformsRecombinant ProteinsTranscription FactorsTretinoinTumor Suppressor Proteins

Identifiers

PMID11042692
OpenAlexW2312341819

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.