Evidence map›Paper›PMID 22678923›Full record

ArticleEMBO molecular medicine2012

p53 suppresses type II endometrial carcinomas in mice and governs endometrial tumour aggressiveness in humans.

Peter J Wild, Kristian Ikenberg, Thomas J Fuchs, Markus Rechsteiner, Strahil Georgiev, Niklaus Fankhauser, Aurelia Noske, Matthias Roessle, Rosmarie Caduff, Athanassios Dellas and 4 more

Open access · goldAbstract read
In one paragraph

Article in EMBO molecular medicine, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
2.7field-weighted citation impact, top 9% 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

35 citing papers in PubMed, 1 synthesis or guideline pooled it, 69 citations in OpenAlex.

  1. Pooled it
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  16. Endometrial cancer: a genetic point of view.Translational cancer research · 2020
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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

14 authors at 6 institutions in 2 countries.

Peter J WildInstitute of Surgical Pathology, University Hospital Zurich, Zurich, Switzerland.
Kristian Ikenberg
Thomas J Fuchs
Markus Rechsteiner
Strahil Georgiev
Niklaus Fankhauser
Aurelia Noske
Matthias Roessle
Rosmarie Caduff
Athanassios Dellas
Daniel Fink
Holger Moch
Wilhelm Krek
Ian J Frew
University Hospital of Zurich · CHUniversity of Zurich · CHETH Zurich · CHCalifornia Institute of Technology · USSwiss Integrative Center for Human Health · CHUniversity Hospital of Basel · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Type II endometrial carcinomas are a highly aggressive group of tumour subtypes that are frequently associated with inactivation of the TP53 tumour suppressor gene. We show that mice with endometrium-specific deletion of Trp53 initially exhibited histological changes that are identical to known precursor lesions of type II endometrial carcinomas in humans and later developed carcinomas representing all type II subtypes. The mTORC1 signalling pathway was frequently activated in these precursor lesions and tumours, suggesting a genetic cooperation between this pathway and Trp53 deficiency in tumour initiation. Consistent with this idea, analyses of 521 human endometrial carcinomas identified frequent mTORC1 pathway activation in type I as well as type II endometrial carcinoma subtypes. mTORC1 pathway activation and p53 expression or mutation status each independently predicted poor patient survival. We suggest that molecular alterations in p53 and the mTORC1 pathway play different roles in the initiation of the different endometrial cancer subtypes, but that combined p53 inactivation and mTORC1 pathway activation are unifying pathogenic features among histologically diverse subtypes of late stage aggressive endometrial tumours.

Indexed as

AnimalsDisease Models, AnimalEndometrial NeoplasmsFemaleGene DeletionHumansMechanistic Target of Rapamycin Complex 1MiceMultiprotein ComplexesProteinsSurvival AnalysisTOR Serine-Threonine KinasesTumor Suppressor Protein p53Mechanistic Target of Rapamycin Complex 1Multiprotein ComplexesProteinsTOR Serine-Threonine KinasesTumor Suppressor Protein p53

Identifiers

PMID22678923
PMCPMC3494078
OpenAlexW1924675596

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.