Evidence map›Paper›PMID 19155295›Full record

ReviewCancer research2009

The transcriptional corepressor CtBP: a foe of multiple tumor suppressors.

G Chinnadurai

Open access · bronzeAbstract readReview
In one paragraph

Review in Cancer research, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 151 papers.

0numbers the graph read from it
0cells of the map it votes in
151citing papers in PubMed
7.3field-weighted citation impact, top 2% 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

151 citing papers in PubMed, 290 citations in OpenAlex.

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91 more citing papers are in PubMed but not listed here.

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

1 author at 1 institution in 1 country.

G ChinnaduraiInstitute for Molecular Virology, Saint Louis University Health Sciences Center, Doisy Research Center, St Louis, Missouri 63104, USA. chinnag@slu.edu
Saint Louis University · US

Funding

Modulation of Oncogenesis by E1A--Role of CtBP and CtIPR01CA084941 · NCI · SAINT LOUIS UNIVERSITY · PI CHINNADURAI, GOVINDASWAMY · 2001 to 2011
$2.5M
NCI NIH HHS CA84941NCI NIH HHS R01 CA084941
6 · The paper itself

Abstract

CtBP1 and CtBP2 are closely related and evolutionarily conserved transcriptional corepressors. There is strong evidence linking CtBPs to tumorigenesis and tumor progression. CtBPs promote epithelial-mesenchymal transition and function as apoptosis antagonists. Also, CtBPs mediate repression of several tumor suppressor genes. Certain tumor suppressors also target CtBPs to restrain their tumor-promoting activity. Down-regulation of CtBPs mediated by some tumor suppressors results in p53-independent apoptosis and reduced tumor cell migration and invasion. The role of CtBPs in modulating the activities of different tumor suppressors is reviewed here. The results discussed here suggest that CtBPs may constitute a novel p53-independent anticancer target.

Indexed as

Alcohol OxidoreductasesAnimalsCell Transformation, NeoplasticDNA-Binding ProteinsHumansNeoplasmsRepressor ProteinsAlcohol OxidoreductasesC-terminal binding proteinDNA-Binding ProteinsRepressor Proteins

Identifiers

PMID19155295
PMCPMC4367538
OpenAlexW2153481815

What OpenQuestion holds

Textmetadata
LicenceTDM
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.