Evidence map›Paper›PMID 8440237›Full record

ArticleThe EMBO journal1993

mdm2 expression is induced by wild type p53 activity.

Y Barak, T Juven, R Haffner, M Oren

Open access · greenAbstract read
In one paragraph

Article in The EMBO journal, 1993. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 505 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
505citing papers in PubMed, 3 pooled it
25.4field-weighted citation impact, top 1% 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

505 citing papers in PubMed, 3 syntheses or guidelines pooled it, 1,285 citations in OpenAlex.

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445 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

4 authors at 1 institution in 1 country.

Y BarakDepartment of Chemical Immunology, Weizmann Institute of Science, Rehovot, Israel.
T Juven
R Haffner
M Oren
Weizmann Institute of Science · IL

Funding

FUNCTIONAL ANALYSIS OF THE P53 CELLULAR TUMOR ANTIGENR01CA040099 · NCI · WEIZMANN INSTITUTE OF SCIENCE · PI OREN, MOSHE · 1985 to 2002
$546k
NCI NIH HHS R01 CA40099
6 · The paper itself

Abstract

We have recently characterized a 95 kDa protein, p95, which exhibits enhanced binding to temperature-sensitive p53 (ts-p53) when cells are shifted down to 32.5 degrees C, a temperature at which ts-p53 possesses wild-type (wt)-like activities. In the present study we show that p95 is a product of the mdm2 putative proto-oncogene. The enhanced complex formation of mdm2 with ts-p53 in cells maintained at 32.5 degrees C is due to an elevation in total mdm2 protein levels following the temperature shift. We further demonstrate that the induction of mdm2 expression by t p53 activity is at the mRNA level. The induction occurs with very rapid kinetics and does not require de novo protein synthesis, suggesting a direct involvement of p53 in the process. Based on these data and on recent findings implicating p53 as a transcription factor, we suggest that the mdm2 gene is a target for activation by wt p53. In view of the ability of mdm2 to act as a specific antagonist of p53 activity, this induction process may serve to tightly autoregulate p53 activity in living cells.

Indexed as

Gene Expression RegulationGenes, p53Nuclear ProteinsProto-Oncogene ProteinsAnimalsBase SequenceCells, CulturedDNAMolecular Sequence DataNeoplasm ProteinsProto-Oncogene Proteins c-mdm2RatsRNA, MessengerDNAMdm2 protein, ratNeoplasm ProteinsNuclear ProteinsProto-Oncogene ProteinsProto-Oncogene Proteins c-mdm2RNA, Messenger

Identifiers

PMID8440237
PMCPMC413229
OpenAlexW1591281137

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.